What is TRESTOLONE E 100 Deus Medical?

What is TRESTOLONE E 100 Deus Medical?

Manufacturer: Deus Medical

Active Substance: Trestolone Enanthate 100 mg/ml

Pack: 1 Box of 10 Ampoules, 1ml (1 cc) per Ampoule (150mg/ml)

TRESTOLONE E 100 (Trestolone Enanthate) is the methylated form of Nandrolone which has a much higher potency than Trenbolone, it is popularly considered a mix between Trenbolone and Nandrolone, being the most powerful steroid that exists.

It is a compound that aromatizes heavily, so if it is used, it should be taken into account to regulate estradiol using different strategies that are not normally applied with normal compounds, or using reduced doses.

It is not reduced to DHT.

It is the compound milligram per milligram with the highest inhibition constant, in fact one of the uses of this substance is as a male contraceptive.

CABERMED 0.5 Deus Medical

Active Substance: Cabergoline (0.5 mg/tab)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (0.5 mg per Tablet)

Form: Oral

What Is Cabergoline (CABERMED 0.5)?

Cabergoline is a potent compound classified as a dopamine receptor agonist (specifically targeting the D2 and D3 receptors). It belongs to a group of drugs known as prolactin inhibitors.

Its primary physiological function is to suppress the release of the hormone Prolactin by the pituitary gland. Clinically, it is used to treat hyperprolactinemia (excessive prolactin) and to prevent lactation (milk production).

Critical Role in Steroid Cycles

For athletes and bodybuilders, Cabergoline is an essential ancillary component when cycling with 19-nor anabolic steroids such as Nandrolone (Deca-Durabolin, NPP) and Trenbolone. These compounds are notorious for significantly increasing prolactin levels.

• Prevents Sexual Dysfunction: High prolactin levels, particularly when testosterone is suppressed, are the direct cause of severe libido loss and erectile dysfunction (often termed "Deca Dick" or "Tren Dick"). Cabergoline effectively suppresses prolactin to prevent these issues.

• Mitigates Gynecomastia Risk: High prolactin can potentiate the effects of estrogen, leading to prolactin-induced gynecomastia. Controlling prolactin minimizes this risk.

Usage and Dosage Protocols

Cabergoline's long half-life means it requires very infrequent dosing.

• Typical Performance Dosage: Due to its potency, the dosage is usually very low: 0.25 mg to 0.5 mg administered just one to two times per week.

• Administration: It is best taken with a meal to minimize the risk of gastrointestinal upset.

• Timing: Cabergoline is used proactively throughout the duration of any cycle involving Nandrolone or Trenbolone.

 Side Effects and Management

Cabergoline is generally well-tolerated, but proper dosing is crucial to avoid severe side effects.

• Common Side Effects: Nausea, dizziness, headache, and potential temporary drops in blood pressure (orthostatic hypotension).

• Dosing Sensitivity: Using too high a dose can suppress prolactin too much, which can also be unhealthy and lead to side effects like mood changes or lethargy. Users should start low and increase only if symptoms warrant.

 Frequently Asked Questions (FAQs)

1. Why is Cabergoline preferred over Bromocriptine for prolactin control?

Cabergoline is strongly preferred over older dopamine agonists like Bromocriptine primarily due to its significantly longer half-life and superior side effect profile. Cabergoline requires dosing only once or twice per week, whereas Bromocriptine often requires daily dosing and is associated with more severe gastrointestinal issues and nausea.

2. Is Cabergoline necessary if I only use Testosterone?

No, Cabergoline is not necessary if you only use Testosterone. Testosterone itself does not significantly raise prolactin levels. Cabergoline is strictly reserved for cycles involving 19-nor derivatives like Nandrolone (Deca-Durabolin) or Trenbolone, which are the primary culprits for prolactin elevation.

3. How do I know if my prolactin levels are too high?

The most common symptoms indicating high prolactin during a cycle include: severe libido suppression, difficulty achieving or maintaining an erection, and in rare cases, lactation (discharge from the nipples). Blood work is the most reliable method for confirming elevated prolactin levels, but symptoms often guide initial dosing.

4. What is the risk of crashing prolactin levels too low?

The risk of suppressing prolactin too low is significant. Prolactin is still essential for immune function and overall well-being. Side effects of overly low prolactin can include fatigue, irritability, mood changes, and reduced immune response. This is why low, infrequent dosing (0.5 mg 1–2 times per week) is critical.

CIAMED 5 PDE5 INHIBITOR Deus Medical

Active Substance: Tadalafil (5 mg/tab)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (5 mg per Tablet)

Form: Oral

What Is Tadalafil (CIAMED 5)?

CIAMED 5 is a medication containing the active substance Tadalafil, which belongs to a class of drugs known as PDE5 Inhibitors.¹ Tadalafil works by relaxing the smooth muscles of blood vessels, thereby increasing blood flow to specific areas of the body.²

This low-dose 5 mg format is primarily utilized for its therapeutic benefits in two key areas:

1. Erectile Dysfunction (Impotence): Tadalafil is highly effective at treating ED by facilitating erections upon sexual stimulation.³

2. Benign Prostatic Hypertrophy (BPH): It is also used to treat the symptoms associated with an enlarged prostate.⁴

How Tadalafil Works

As a PDE5 Inhibitor, Tadalafil operates by blocking the Phosphodiesterase Type 5 enzyme.⁵ This action prevents the degradation of cGMP, a substance that signals smooth muscles to relax.⁶ When blood vessels in the penis are relaxed, circulation improves, leading to a firm erection in the presence of sexual arousal.

Key Advantage: Long Duration and Daily Use

Tadalafil's unique half-life makes it distinct among PDE5 inhibitors:

• Extended Duration: Tadalafil can remain active for up to 36 hours, earning it the nickname "The Weekend Pill" in higher doses.⁷

• Low-Dose Daily Use: The 5 mg tablet is ideal for once-daily administration, providing constant therapeutic support.⁸ This allows for increased spontaneity and continuous treatment for BPH symptoms.

 Usage and Dosage

• Standard Therapeutic Dosage: The suggested dosage for daily use is 5 mg daily, taken orally.⁹

• Timing: For daily BPH or spontaneity support, the tablet should be taken at the same time each day.

 Side Effects and Safety Warning

Tadalafil is generally well-tolerated.¹⁰ Common side effects can include headache, indigestion, back pain, and muscle aches, which usually subside after a few hours.¹¹

Warning: Tadalafil should never be used with nitrate components (often prescribed for chest pain/angina), as this combination can cause a dangerous drop in blood pressure.¹² Individuals with heart conditions or low blood pressure should consult a physician before use.

 Frequently Asked Questions (FAQs)

1. What is the main benefit of using Tadalafil at 5 mg daily instead of a higher dose (20 mg) as needed?

The primary benefit of the 5 mg daily dose is continuous therapeutic support and spontaneity. The user doesn't have to plan the dosage ahead of sexual activity, as the drug's effects are present constantly. It is also the preferred dosage for managing the daily symptoms of Benign Prostatic Hypertrophy (BPH).

2. Is Tadalafil (CIAMED 5) used by bodybuilders for purposes other than ED?

Yes. Due to its vasodilatory (blood vessel relaxing) properties, Tadalafil is sometimes used by athletes for its ability to increase muscular pumps and nutrient delivery during workouts.¹³ This increased blood flow is also believed to help mitigate cardiovascular strain associated with certain anabolic steroids.

3. Does Tadalafil interact with Anti-Estrogens or SERMs used in PCT?

No, Tadalafil does not typically interact negatively with SERMs (like Nolvadex) or Aromatase Inhibitors (AIs) used during Post Cycle Therapy (PCT). In fact, it is often used during and after a steroid cycle to combat potential libido issues caused by hormonal suppression or imbalances.

4. How long does it take for the 5 mg daily dosage to reach full effectiveness?

When starting daily Tadalafil, stable blood concentration (and thus maximum effectiveness for ED/BPH) is typically reached after 4 to 5 days of continuous use. This steady concentration is what provides the 24/7 therapeutic benefit.

ENCLOMIMED 25 Deus Medical (Enclomiphene Citrate): The Pure PCT Component

Active Substance: Enclomiphene Citrate ($25 \text{ mg/tab}$)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets

Form: Oral

What Is Enclomiphene Citrate?

Enclomiphene Citrate is the pharmacologically active isomer of the drug Clomiphene Citrate (Clomid). Traditional Clomiphene is a ¹$50/50$ mixture of two isomers: Enclomiphene (the active, beneficial component) and Zuclomiphene (the less active component often linked to side effects).²

ENCLOMIMED 25 provides the pure Enclomiphene isomer, making it a highly targeted component preferred for restoring hormonal balance during Post Cycle Therapy (PCT).

Core Functions and Superiority in PCT

Enclomiphene belongs to the class of Selective Estrogen Receptor Modulators (SERMs). Its function is crucial for speeding up recovery after the severe hormonal suppression caused by anabolic steroid use.

1. Superior Testosterone Restoration

Enclomiphene works by selectively blocking estrogen receptors in the hypothalamus and pituitary gland. This action prevents estrogen from inhibiting the pituitary, effectively "tricking" the brain into believing estrogen levels are low.³

This signaling dramatically increases the release of:

• Luteinizing Hormone (LH)

• Follicle-Stimulating Hormone (FSH)

LH and FSH are the direct triggers for the testes to restart and significantly boost the production of natural testosterone.⁴

2. Reduced Side Effects

The main advantage is purity. By eliminating the less desirable Zuclomiphene isomer, which has a longer half-life and is often linked to side effects, pure Enclomiphene is theorized to have a lower rate of adverse effects, particularly those affecting mood and vision, compared to traditional Clomiphene.⁵

Usage and Dosage Protocols

Enclomiphene is highly effective at a lower dosage than the mixed-isomer Clomiphene.⁶

• Dosage: A common dosage for PCT is ⁷$25 \text{ mg}$ to ⁸$50 \text{ mg}$ per day.⁹ The $25 \text{ mg}$ tablets allow for precise titration. Functionally, $25 \text{ mg}$ of pure Enclomiphene is equivalent to $50 \text{ mg}$ of standard Clomiphene.

• Timing: Like all PCT SERMs, Enclomiphene should be started after the active steroid components have dropped to low levels (e.g., 3 weeks after the last long-ester injection).

• Duration: Used for a standard PCT duration of 4 to 6 weeks.

Side Effects

Enclomiphene is generally well-tolerated.¹⁰ Side effects are rare but may include mild headache, nausea, and minor visual disturbances (though the risk is lower due to the removal of the Zuclomiphene isomer).¹¹

 Frequently Asked Questions (FAQs)

1. What is the main advantage of pure Enclomiphene over generic Clomiphene (Clomid)?

The main advantage is purity and side effect reduction. Standard Clomid is a ¹²$50/50$ mix of Enclomiphene (active) and Zuclomiphene (inactive, but with a longer half-life that contributes to vision and mood side effects).¹³ ENCLOMIMED removes the Zuclomiphene, potentially offering the same hormonal benefits with a cleaner, lower-risk profile.

2. Can Enclomiphene be used to fight gynecomastia during the cycle?

Yes, indirectly. As an SERM, Enclomiphene acts by blocking estrogen receptors in the breast tissue, thus preventing estrogen from stimulating tissue growth.¹⁴ While its primary role is PCT, it can be used during a cycle for this protective, anti-gyno effect.

3. Does Enclomiphene still need to be stacked with Nolvadex (Tamoxifen) in PCT?

It is often recommended. While Enclomiphene is highly effective at boosting LH/FSH for testosterone restoration, Nolvadex (Tamoxifen) is considered more potent at directly blocking estrogen receptors in the breast tissue. Combining the two provides a highly effective and robust PCT protocol.

4. Is the $25 \text{ mg}$ dose of Enclomiphene equal to the $50 \text{ mg}$ dose of Clomiphene?

Yes, functionally. Since standard $50 \text{ mg}$ Clomiphene is only $50\%$ Enclomiphene, the $25 \text{ mg}$ of pure Enclomiphene (ENCLOMIMED 25) provides the exact same amount of the desired active isomer, ensuring full effectiveness with less of the unnecessary isomer.

EZETIMED 10 Deus Medical

Active Substance: Ezetimibe (10 mg/tab)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (10 mg per Tablet)

Form: Oral

What Is Ezetimibe (EZETIMED 10)?

Ezetimibe is a medication used to treat and manage high cholesterol levels.² It is unique because it works through a mechanism fundamentally different from statins (which block cholesterol production in the liver).

Ezetimibe is a potent Cholesterol Absorption Inhibitor.³ It effectively lowers the levels of total cholesterol, "bad" cholesterol ($\text{LDL}$ cholesterol), and triglycerides circulating in the blood, while simultaneously raising levels of "good" cholesterol ($\text{HDL}$ cholesterol).

Core Functions and Mechanism

Ezetimibe works by reducing the absorption of cholesterol in the digestive tract.⁴

• Selective Inhibition: It acts on the intestinal brush border, specifically inhibiting the Niemann-Pick C1-Like 1 (⁵$\text{NPC}1\text{L}1$) transport protein.⁶ This protein is responsible for absorbing cholesterol from the small intestine.⁷

• Lowered Circulating Cholesterol: By blocking this absorption pathway, Ezetimibe reduces the amount of dietary and biliary cholesterol that enters the bloodstream, resulting in lower circulating ⁸$\text{LDL}$ levels.⁹

• Synergistic Effect: Ezetimibe adds significantly to the cholesterol-lowering effect of statins, a group of drugs that lower cholesterol made by the body.¹⁰ Combining Ezetimibe and a statin targets both sources of cholesterol (absorption and production).

Usage and Dosage Protocols

Ezetimibe is designed for simple, once-daily administration.¹¹

• Recommended Dosage: The standard dose is one Ezetimibe ¹²$10 \text{ mg}$ tablet orally once a day.¹³

• Administration: It can be taken at any time of the day, with or without food.¹⁴

• Combination Therapy: If taken alongside a statin, both medications can be consumed at the same time.¹⁵

 Side Effects and Precautions

Ezetimibe is generally well-tolerated.¹⁶ When used alone, side effects are usually minor. However, when combined with a statin, the risk of statin-related side effects (such as muscle aches or liver enzyme elevation) may increase. Individuals with liver disease should consult a physician before use.

 Frequently Asked Questions (FAQs)

1. Why is Ezetimibe relevant to anabolic steroid users?

Anabolic steroids, particularly oral and ¹⁷$\text{DHT}$-derived components, are known to negatively impact the lipid profile (cholesterol), often severely lowering ¹⁸$\text{HDL}$ (good cholesterol) and raising ¹⁹$\text{LDL}$ (bad cholesterol).²⁰ Ezetimibe is used to help mitigate this steroid-induced cardiovascular strain by directly lowering the problematic $\text{LDL}$ component in the blood.

2. Does Ezetimibe interfere with the effectiveness of anabolic steroids?

No. Ezetimibe's mechanism is confined to the digestive tract and selectively targets cholesterol absorption.²¹ It does not interfere with the hormonal pathways or androgen receptors, meaning it can be safely used during an anabolic steroid cycle to protect cardiovascular health without diminishing muscle gains.

3. If Ezetimibe is taken with a statin, does the dosage need to be split?

No. The product information explicitly states that if Ezetimibe is taken along with a statin, both drugs can be taken at the same time. This simplifies the daily regimen for patients utilizing combination therapy to achieve maximum $\text{LDL}$ reduction.

4. How long does it take for Ezetimibe to start lowering cholesterol levels?

Ezetimibe acts quickly by blocking the absorption pathway, and its $\text{LDL}$-lowering effect typically becomes noticeable within one to two weeks of starting therapy, reaching its maximum effect within about four weeks.

Livamed 1 Deus Medical (Pitavastatin): Potent HMG-CoA Reductase Inhibitor

Active Substance: Pitavastatin Calcium ($1 \text{ mg/tab}$)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets ($1 \text{ mg}$ per Tablet)

Form: Oral

What Is Pitavastatin?

Pitavastatin belongs to the class of medications known as statins, or ¹$\text{HMG-CoA}$ reductase inhibitors.² It is used to lower high cholesterol and triglyceride levels and is considered one of the newer, more potent statins available.³

Pitavastatin works by blocking the enzyme ⁴$\text{HMG-CoA}$ reductase in the liver.⁵ This enzyme is the rate-limiting step in the body's natural production of cholesterol. By inhibiting this process, Pitavastatin effectively reduces the total amount of "bad" cholesterol (⁶$\text{LDL}$) in the bloodstream.⁷

Core Functions and Mechanism

• $\text{LDL}$ Reduction: The primary function is to significantly reduce levels of $\text{LDL}$ cholesterol, which is essential for reducing the risk of cardiovascular events like heart attack and stroke.

• High Potency: Pitavastatin is known to be highly effective at low doses, often achieving the same therapeutic effect as higher doses of older statins.

• Metabolic Profile: It exhibits minimal metabolism through the ⁸$\text{CYP}3\text{A}4$ pathway in the liver, which reduces the potential for drug interactions compared to many other statins.⁹

• Cardiovascular Protection: By improving the lipid profile (lowering ¹⁰$\text{LDL}$ and triglycerides), it helps prevent the build-up of plaque in the arteries.¹¹

 Usage and Dosage Protocols

Pitavastatin is a prescription medication and must be taken according to medical guidance.¹²

• Recommended Dosage: The standard starting dosage for Pitavastatin is typically ¹³$1 \text{ mg}$ to ¹⁴$2 \text{ mg}$ once daily.¹⁵ The $1 \text{ mg}$ tablet allows for precise control over dosing.

• Administration: Typically taken once a day, with or without food.

• Monitoring: Regular blood tests are necessary to monitor lipid levels and check for potential side effects, such as elevated liver enzymes.¹⁶

 Side Effects and Warnings

Like all statins, Pitavastatin carries a risk of side effects, primarily affecting muscle and liver tissue.¹⁷

• Myopathy/Rhabdomyolysis: The most serious, though rare, side effect is rhabdomyolysis (severe muscle breakdown), often preceded by muscle aches and weakness (myopathy). Users must report unexplained muscle pain or weakness to a physician immediately.

• Liver Enzymes: Statins can cause elevation of liver enzymes (¹⁸$\text{ALT}$ and ¹⁹$\text{AST}$).²⁰

• Other Side Effects: Headache, constipation, and common cold symptoms are possible.

Frequently Asked Questions (FAQs)

1. Why is Pitavastatin relevant to anabolic steroid users?

Anabolic steroids severely worsen the lipid profile (cholesterol), drastically lowering protective ²¹$\text{HDL}$ and raising harmful ²²$\text{LDL}$.²³ Pitavastatin is used by some athletes to aggressively combat this steroid-induced $\text{LDL}$ elevation and mitigate the associated cardiovascular risks during a cycle.

2. Is Pitavastatin more potent than other statins?

Yes. Pitavastatin is considered one of the most potent statins on a per-milligram basis.²⁴ This high potency means that very low dosages (like $1 \text{ mg}$) can achieve significant $\text{LDL}$ reduction compared to the starting doses of older statins.

3. Should Pitavastatin be taken at night or in the morning?

Unlike some older, shorter-acting statins (which must be taken at night because cholesterol production peaks then), Pitavastatin is a long-acting statin.²⁵ It can be taken effectively at any time of the day due to its prolonged inhibitory effect on the ²⁶$\text{HMG-CoA}$ reductase enzyme.²⁷

4. How does Pitavastatin differ from Ezetimibe (EZETIMED 10)?

They work differently:

• Pitavastatin (LIVAMED 1): Works in the liver to block the production of cholesterol (²⁸$\text{HMG-CoA}$ reductase inhibitor).²⁹

• Ezetimibe: Works in the intestine to block the absorption of cholesterol.30

  They are often used together to target both sources of cholesterol effectively.31

PRILIMED 30 (Dapoxetine HCl): Fast-Acting Treatment for Premature Ejaculation

Active Substance: Dapoxetine HCl ($30 \text{ mg/tab}$)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets ($30 \text{ mg}$ per Tablet)

Form: Oral

What Is Dapoxetine HCl (PRILIMED 30)?

PRILIMED 30 contains Dapoxetine Hydrochloride, a medication specifically developed and used for the treatment of premature ejaculation (²$\text{PE}$) in men.³

Dapoxetine belongs to the class of drugs known as Selective Serotonin Reuptake Inhibitors (⁴$\text{SSRIs}$).⁵ Its unique property is its short-acting nature, which allows it to be taken on demand, shortly before sexual activity, unlike other ⁶$\text{SSRIs}$ that require chronic daily dosing for mood disorders.⁷

Core Functions and Mechanism

• Ejaculation Control: Dapoxetine works by inhibiting the reuptake of serotonin in the synaptic cleft.⁸ Increased serotonin levels in the central nervous system (⁹$\text{CNS}$) help to increase the time required to reach ejaculation, thereby improving control and satisfaction.¹⁰

• Short-Acting Profile: Dapoxetine is absorbed and eliminated rapidly.¹¹ Its rapid onset (¹²$\sim 1 \text{ hour}$) and quick clearance means it does not accumulate in the body, minimizing the long-term side effects typically associated with chronic ¹³$\text{SSRI}$ use.¹⁴

 Usage and Dosage Protocols

Dapoxetine is used on an as-needed basis only, immediately prior to sexual activity.¹⁵

• Recommended Starting Dose: The recommended initial starting dose is ¹⁶$30 \text{ mg}$.¹⁷

• Timing: The dose should be taken as needed, approximately 1 to 3 hours before sexual activity.¹⁸

• Maximum Dose: If the response to ¹⁹$30 \text{ mg}$ is insufficient and the user has not experienced moderate or severe adverse reactions, the dose may be increased to a maximum recommended dose of ²⁰$60 \text{ mg}$.²¹

• Frequency: Dapoxetine should not be used chronically on a daily basis and should not be taken more frequently than once every 24 hours.²²

• Caution: The incidence and severity of adverse events are greater at the ²³$60 \text{ mg}$ dose.²⁴

 Side Effects and Warnings

As an ²⁵$\text{SSRI}$, Dapoxetine can cause side effects related to the central nervous system (²⁶$\text{CNS}$).²⁷

• Common Side Effects: Dizziness, headache, nausea, and diarrhea are common, particularly at higher doses.²⁸

• Syncope Risk: There is a risk of syncope (fainting), often preceded by prodromal symptoms (like dizziness or palpitations).²⁹ Users should be aware of these symptoms, especially when increasing the dose.

• Drug Interactions: Dapoxetine may interact with other medications, particularly other ³⁰$\text{SSRIs}$, ³¹$\text{MAO}$ inhibitors, and certain antifungal drugs.³²

 Frequently Asked Questions (FAQs)

1. Why is Dapoxetine considered unique among $\text{SSRIs}$?

Dapoxetine is unique because it is specifically designed to be short-acting.³³ Its rapid absorption and elimination mean it is suitable for on-demand use shortly before sexual activity.³⁴ Other $\text{SSRIs}$ (used for depression) have long half-lives and must be taken daily for weeks to become effective, making them unsuitable for episodic $\text{PE}$ treatment.

2. Can Dapoxetine be stacked with a $\text{PDE}5$ Inhibitor (like Tadalafil)?

Yes, it is common. Dapoxetine treats the timing issue ($\text{PE}$), while a $\text{PDE}5$ inhibitor (like Tadalafil or Sildenafil) treats the erection quality issue ($\text{ED}$). Because the two drugs target different mechanisms, they are often used together to address both aspects of male sexual dysfunction.

3. Should I take Dapoxetine every day for better results?

No. Dapoxetine is designed to be taken as needed.³⁵ Chronic, daily use is not recommended and increases the risk of side effects associated with continuous $\text{SSRI}$ activity. It should be taken $1 \text{ to } 3 \text{ hours}$ before the anticipated sexual activity.

4. What are the signs that I should not increase my dose from $30 \text{ mg}$ to $60 \text{ mg}$?

You should not increase the dose if you have experienced any moderate or severe adverse reactions or any prodromal symptoms suggestive of syncope (e.g., sudden sweating, lightheadedness, dizziness, or palpitations) while taking the $30 \text{ mg}$ dose. Given the higher risk profile of the $60 \text{ mg}$ dose, caution is strongly advised.

Supermed 10 Deus Medical
 

Methyldrostanolone (Supermed 10) is one of the most potent oral anabolic steroids available, valued for providing dramatic muscle hardness, fullness, and strength gains, particularly in the final weeks before a competition.

I will search for more detailed information regarding its full chemical name, its androgenic/anabolic ratings, and the specific liver toxicity profile due to its C-17aa modification.

Methyldrostanolone, commonly known by the nickname Superdrol, is one of the most effective and powerful oral anabolic steroids (AAS).1 It is a derivative of Drostanolone (Masteron) that is structurally modified for oral use, making it highly potent for dramatic strength gains and muscular hardness.2

What Is Methyldrostanolone (Supermed 10)?

SUPERMED 10 contains the active substance Methyldrostanolone (also known as Methasterone).³ It is a synthetic, orally active anabolic-androgenic steroid that was never marketed for medical use but was sold illicitly as a "designer steroid."⁴

Core Functions and Extreme Potency

• Chemical Classification: Methyldrostanolone is a ⁵$17\alpha$-alkylated derivative of dihydrotestosterone (⁶$\text{DHT}$).⁷ It is essentially Drostanolone (Masteron) with a ⁸$17\alpha$-methyl group for oral bioavailability.⁹

• Anabolic/Androgenic Ratio: Research indicates Methyldrostanolone is a potent orally active anabolic agent exhibiting only weak androgenic activity.¹⁰ This favorable ratio is highly sought after for gaining lean, high-quality muscle.

• Physique Enhancement: It is widely used before competitions as a "finisher" for its dramatic fullness and hardening effect on muscle tissue.

• Non-Aromatizing: Methyldrostanolone lacks estrogenic activity, meaning it does not aromatize into estrogen. This eliminates the risk of estrogen-related side effects like water retention and gynecomastia.

 Usage, Dosage, and CRITICAL Liver Toxicity

Methyldrostanolone is one of the most hepatotoxic (liver-toxic) oral steroids available and should be used with extreme caution.

• Dosage: Most users begin with a low dosage of $10 \text{ mg}$ to $40 \text{ mg}$ per day.

• Duration: Cycles are strictly limited to 4–8 weeks.

• Mechanism of Toxicity: As an $\text{C-}17\alpha\text{aa}$ modified oral steroid, it survives the first pass through the liver. This process is highly stressful, leading to severe cholestatic liver injury (jaundice, pruritus) and can be associated with acute renal failure.¹¹

Critical Warning: Methyldrostanolone is well-documented in medical literature as a growing cause of severe AAS-induced liver injury (¹²$\text{DILI}$).¹³ Patients often present with symptoms long after stopping the compound, and recovery can take up to 3 months. Liver protection supplements (like Milk Thistle/NAC) are considered mandatory, but may not fully mitigate the risk.

Side Effects and Management

Despite its lack of estrogenic activity, Methyldrostanolone carries significant risks.

• Hepatotoxicity (Severe): The most common serious side effect is liver damage, often characterized by high bilirubin levels and jaundice.¹⁴

• Androgenic Effects: Possible side effects include acne, oily skin, and accelerated male pattern hair loss (due to its ¹⁵$\text{DHT}$-derived nature).¹⁶

• Hormonal Suppression: Methyldrostanolone severely suppresses natural testosterone production (hypogonadism).¹⁷ This requires a mandatory Post Cycle Therapy (PCT) protocol to restore the body's hormonal balance.

• Cardiovascular: It can adversely affect cholesterol levels ($\text{HDL}$ and $\text{LDL}$), increasing the risk of cardiovascular issues.

Frequently Asked Questions (FAQs)

1. Does Supermed 10 require anti-estrogens like Anastrozole?

No. Methyldrostanolone has no estrogenic activity; it cannot convert into estrogen. Therefore, you do not need an Aromatase Inhibitor ($\text{AI}$) to manage estrogen-related side effects like water retention or gynecomastia from this compound.

2. Is Methyldrostanolone safer for the liver than other $\text{C-}17\alpha\text{aa}$ orals?

No. Medical case reports indicate that Methyldrostanolone is one of the most common and severe causes of ¹⁸$\text{AAS}$-induced liver injury, often leading to pronounced cholestasis and jaundice.¹⁹ It is considered one of the most toxic oral steroids available.

3. Why must a cycle of Supermed 10 be so short (4–8 weeks)?

The cycle must be short to minimize the risk of irreversible liver damage and severe cholestasis. The toxicity accumulates rapidly, and prolonged use significantly increases the chance of developing life-threatening complications.

4. Is Supermed 10 known for giving high-quality muscle gains?

Yes. Methyldrostanolone is prized for its ability to produce dry, hard, and high-quality gains. Since it does not cause water retention, the muscle mass gained is dense and permanent (assuming maintenance training and nutrition).

TELMIMED 40 (Telmisartan): Angiotensin II Receptor Blocker (ARB)

Active Substance: Telmisartan (40 mg/tab)
Manufacturer: Deus Medical
Pack: 1 Box of 2x 25 Tablets (40 mg per Tablet)
 Form: Oral  

What Is Telmisartan?

Telmisartan (TELMIMED 40) is a prescription medication belonging to the class of drugs known as Angiotensin II Receptor Blockers (ARBs). It is primarily used to treat and manage hypertension (high blood pressure) and reduce the risk of stroke, heart attack, and death in high-risk patients.  

Telmisartan works by blocking the action of Angiotensin II, a potent hormone that causes blood vessels to constrict and elevate blood pressure.  

Core Functions and Unique Advantages

• Angiotensin II Blockade: Telmisartan selectively blocks the AT1​ receptor, preventing the binding of Angiotensin II. This results in vasodilation (widening of blood vessels) and reduced blood pressure.  

• Long Half-Life: Telmisartan has one of the longest half-lives among ARBs (around 24 hours), allowing for effective, once-daily dosing.  

• PPAR-Gamma Modulation: Telmisartan exhibits a unique partial agonist activity on the PPAR-gamma receptor (Peroxisome Proliferator-Activated Receptor gamma). This activity gives it potential secondary benefits for metabolic health, including improved insulin sensitivity and lipid profiles (cholesterol/triglycerides).  

• Cardiovascular Protection: By reducing vascular resistance and lowering blood pressure, it reduces the overall workload on the heart.

Usage and Dosage Protocols

Telmisartan is a prescription medication and must be taken strictly under medical supervision.  

• Standard Therapeutic Dosage: The typical starting dosage for hypertension is 40 mg once daily. The dosage may be adjusted upward based on individual blood pressure response.  

• Administration: Taken orally once per day, with or without food.  

• Monitoring: Regular monitoring of blood pressure and kidney function is required while on this medication.

 Side Effects and Warnings

Like all prescription ARBs, Telmisartan carries specific safety considerations.

• Common Side Effects: Dizziness, fatigue, back pain, and cold or flu-like symptoms.  

• Kidney Function: ARBs should be used with caution in patients with existing renal (kidney) impairment.

• Hypotension: May cause excessive lowering of blood pressure, especially in patients who are dehydrated or volume-depleted.  

• Contraindications: Should not be used during pregnancy, as ARBs can cause injury and death to the developing fetus.  

Frequently Asked Questions (FAQs)

1. Why is Telmisartan relevant to anabolic steroid users?

Anabolic steroid use often leads to hypertension (high blood pressure) due to increased blood volume and cardiovascular strain. Telmisartan is sometimes misused by athletes to manage this steroid-induced hypertension and leverage its unique PPAR-gamma activity for potential metabolic benefits (e.g., improved nutrient partitioning).  

2. Is Telmisartan a diuretic (water pill)?

No. Telmisartan is an ARB that lowers blood pressure by blocking a hormone (Angiotensin II) that constricts vessels. While ARBs can cause a slight reduction in fluid retention as a secondary effect of lowered pressure, it is not a primary diuretic and does not work directly on the kidneys like a water pill.  

3. What does the PPAR-gamma modulation mean for metabolic health?

PPAR-gamma is a receptor that plays a major role in fatty acid metabolism, glucose uptake, and insulin sensitivity. Telmisartan's partial activation of this receptor means it has therapeutic potential beyond just blood pressure control, including improving how the body manages blood sugar and lipids (cholesterol).  

4. Is Telmisartan safe to take with other performance-enhancing drugs?

No. Combining Telmisartan with other drugs that lower blood pressure, affect electrolytes, or strain the kidneys (like high-dose steroids or some SARMs) can be dangerous. Its use should be strictly managed by a healthcare provider who is aware of all concomitant medications and health conditions.

VIAMED 20 PDE5 INHIBITOR Deus Medical 

VIAMED 20 PDE5 INHIBITOR Deus Medical is a pharmaceutical-grade Sildenafil citrate product created to support healthy blood flow and improve erectile function. Manufactured by Deus Medical, this product contains 20 mg of Sildenafil citrate per tablet and comes in a large pack of 2 x 25 tablets, offering excellent value and consistent dosing. In this guide, we explore how VIAMED 20 works, its benefits, safety instructions, and who can use it.

What Is VIAMED 20 PDE5 INHIBITOR Deus Medical?

VIAMED 20 PDE5 INHIBITOR Deus Medical is a potent PDE5 inhibitor designed to improve blood flow by relaxing smooth muscle tissue. Sildenafil citrate, the active substance, is well-known for its effectiveness in treating erectile dysfunction (ED) and improving vascular response.

Manufacturer Background – Deus Medical

Deus Medical is a respected international brand known for producing reliable medical-grade compounds, oral tablets, and hormone-related products. Their strict testing standards ensure that each VIAMED 20 tablet delivers accurate dosing and dependable quality.

Summary of Key Specifications

• Active ingredient: Sildenafil citrate

• Strength: 20 mg per tablet

• Pack size: 1 box containing 2 blister packs of 25 tablets each

• Category: PDE5 inhibitor

• Manufacturer: Deus Medical

Active Ingredient: Sildenafil Citrate 20mg Explained

Sildenafil citrate is a well-studied medication used for improving erection quality and blood flow.

How Sildenafil Works in the Body

Sildenafil is a PDE5 enzyme inhibitor. PDE5 breaks down cGMP, a compound responsible for relaxing blood vessels. By blocking PDE5, Sildenafil boosts cGMP levels, allowing more blood to flow into targeted areas—especially the penile tissue.

Medical Uses of Sildenafil

• Erectile dysfunction (ED)

• Improving blood circulation

• Supporting vascular health

• Some off-label uses for performance circulation issues

Product Packaging and Format

Tablet Strength Details

Each tablet contains 20 mg of pure Sildenafil citrate—ideal for users who require flexible dosing.

Advantages of Multi-Pack Structure

The 2 x 25 tablet packaging offers:

• Long-term supply

• Cost-effectiveness

• Easy dosage adjustment

• Convenient storage

How VIAMED 20 PDE5 INHIBITOR Works

VIAMED 20 PDE5 INHIBITOR Deus Medical functions by enhancing natural blood flow responses.

Increasing Blood Flow

It promotes vasodilation, allowing smoother circulation to targeted tissues.

Duration and Onset

• Onset: 30–60 minutes

• Effect duration: 4–6 hours (may vary)

Proper Dosage Guidelines

While medical guidance is always recommended, general dosing suggestions include:

Starting Dose Recommendations

Most adults begin with 20 mg to 40 mg, depending on sensitivity and needs.

Maximum Daily Dosage

Do not exceed 100 mg per day unless instructed by a physician.

Benefits of Choosing VIAMED 20 PDE5 INHIBITOR Deus Medical

Quality & Purity Standards

Deus Medical uses strict testing and lab-grade manufacturing.

Consistent Tablet Potency

Each tablet is accurately dosed for predictable and reliable performance.

Safety Precautions and Side Effects

Mild Side Effects

Possible mild effects include:

• Headache

• Flushing

• Nasal congestion

• Light dizziness

When Not to Use Sildenafil

Do not use if:

• Taking nitrates

• You have severe heart issues

• You’re allergic to Sildenafil

Who Is VIAMED 20 PDE5 INHIBITOR For?

Adults With ED

Its primary use is for treating erectile dysfunction.

Circulation Support (Off-Label)

Some individuals use low-dose Sildenafil for improving circulation or physical performance-related blood flow.

Tips for Best Results

Avoiding Interactions

Avoid:

• Alcohol

• Grapefruit

• Nitrate medications

Timing for Maximum Effectiveness

Take 30–60 minutes before needed.

How to Store VIAMED 20 PDE5 INHIBITOR

• Keep at room temperature

• Store away from moisture

• Keep out of children’s reach

Identifying Genuine Deus Medical Products

• Check holograms

• Inspect batch numbers

• Ensure sealed packaging

FAQs About VIAMED 20 PDE5 INHIBITOR Deus Medical

1. What is the main use of VIAMED 20 PDE5 INHIBITOR Deus Medical?

It is primarily used to treat erectile dysfunction and improve blood flow through the action of Sildenafil citrate.

2. How strong is each VIAMED 20 tablet?

Each tablet contains 20 mg of Sildenafil citrate, allowing flexible and adjustable dosing.

3. How many tablets come in one box?

One box includes 2 blister packs of 25 tablets each, totaling 50 tablets.

Conclusion

VIAMED 20 PDE5 INHIBITOR Deus Medical is a trusted and effective Sildenafil citrate product designed for adults seeking improved blood flow, enhanced performance, and dependable results. With high-quality manufacturing, precise dosing, and generous packaging, it offers excellent long-term value.

If you're looking for reliability, consistency, and potency, VIAMED 20 PDE5 INHIBITOR Deus Medical delivers all three with confidence.

EVIMED 60 SERM Deus Medical (Raloxifene HCl)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (60 mg per Tablet)

Form: Oral

What Is Raloxifene HCl (EVIMED 60)?

Raloxifene Hydrochloride is a compound classified as a Selective Estrogen Receptor Modulator (SERM).² It is a third-generation SERM that is often considered to be more tissue-selective than older SERMs like Tamoxifen (Nolvadex).

Raloxifene works by selectively acting as an estrogen receptor antagonist (blocker) in some tissues (like breast tissue) while acting as an agonist (activator) in other tissues (like bone).³

Core Functions for Bodybuilders

While Raloxifene is clinically used to prevent and treat osteoporosis in postmenopausal women, its primary utility in the context of performance enhancement is highly targeted:

• Gynecomastia Treatment: Raloxifene is considered one of the most effective prescription options for treating existing gynecomastia (gyno). Research suggests it is highly effective at reducing the size of developing gynecomastia tissue by blocking estrogen's effects on the breast.

• Bone Health Support: Due to its agonist effect in bone tissue, it helps maintain bone density, which can be beneficial during cycles that might negatively impact bone mineral content.⁴

• Alternative to Tamoxifen: It is often utilized by individuals who cannot tolerate the side effects of Tamoxifen (Nolvadex) but still require breast tissue protection.

Usage and Dosage Protocols

Raloxifene is typically used to address specific needs rather than as a general PCT component.

• Gynecomastia Management: Dosages for treating developing or existing gynecomastia symptoms typically range from $30 \text{ mg}$ to $60 \text{ mg}$ per day.

• Duration: Treatment cycles for gynecomastia are often prolonged, running for 3 to 6 months to achieve optimal reduction or reversal of the breast tissue.

• Administration: Typically taken once daily.⁵

 Side Effects and Precautions

Raloxifene is generally well-tolerated, but its selective action means it carries specific risks that must be understood.

• Deep Vein Thrombosis (DVT) Risk: The most significant concern with Raloxifene is a slightly increased risk of blood clotting events (thromboembolism), including deep vein thrombosis (DVT) and pulmonary embolism.⁶

• Common Side Effects: Hot flashes, flu-like symptoms, and leg cramps are the most common reported side effects.

• Hormonal Impact: While it blocks estrogen in the breast, Raloxifene has a less pronounced effect on stimulating the release of LH/FSH (testosterone restoration) compared to Clomiphene or Tamoxifen, limiting its effectiveness as a sole agent for PCT.

Frequently Asked Questions (FAQs)

1. How does Raloxifene (EVIMED) differ from Tamoxifen (Nolvadex) for gynecomastia?

Both are SERMs that block estrogen at the breast. However, Raloxifene is often cited in research as being more potent and effective than Tamoxifen at reducing the size of existing gynecomastia tissue, making it the preferred choice for therapeutic treatment rather than just prevention.

2. Is Raloxifene suitable as a sole agent for Post Cycle Therapy (PCT)?

No. While Raloxifene blocks estrogen receptors in the breast, it has a weaker stimulatory effect on the production of LH and FSH compared to Clomiphene or Tamoxifen. Therefore, it is generally not recommended as the sole agent for PCT, where the primary goal is to fully restore natural testosterone production.

3. What is the major health risk associated with using Raloxifene?

The major risk is an increased chance of thromboembolism (blood clots), including DVT and pulmonary embolism.⁷ Individuals with a history of blood clots or heart issues should strictly avoid Raloxifene, and all users should stay well-hydrated and monitor for symptoms.

4. Should Raloxifene be used during or after a steroid cycle?

Raloxifene can be used during a cycle for gyno prevention if Tamoxifen is not tolerated. However, its most common and valuable use is after the cycle (or post-PCT) as a therapeutic treatment for a prolonged period (3–6 months) to reverse the formation of existing gynecomastia.

FEMAMED 2.5 AROMATASE INHIBITOR Deus Medical

FEMAMED 2.5 by Deus Medical features Letrozole, the most powerful third-generation Aromatase Inhibitor (AI) available.¹ While other inhibitors like Anastrozole are used for general maintenance, Letrozole is often referred to as the "nuclear option" for estrogen control.

In clinical settings, Letrozole is capable of inhibiting the aromatase enzyme by up to 99%. For athletes and bodybuilders, this makes FEMAMED 2.5 an indispensable tool for halting the progression of existing gynecomastia and managing estrogen levels during extremely high-dose anabolic cycles.²

Technical Product Specifications

Core Functions & Extreme Potency

• Total Estrogen Blockade: Letrozole is significantly more potent than Anastrozole or Exemestane, providing the highest level of peripheral estrogen suppression possible.

• Gynecomastia Emergency Treatment: It is the primary choice for reversing early-stage gynecomastia (lumps or puffiness) that has resisted other treatments.

• Maximum Muscle Hardness: By eliminating nearly all systemic water retention, Letrozole can produce an extremely dry, "paper-thin" skin appearance often sought by pro bodybuilders in the final days before a competition.

• Natural Testosterone Stimulation: By removing estrogenic feedback, it signals the pituitary gland to increase the release of LH and FSH, which can sharply raise natural testosterone production.³

Usage & Dosage Protocols

Due to its extreme strength, Letrozole is rarely used at the full 2.5 mg clinical dose by men. Precision dosing is essential to avoid "crashing" your hormones.

Pro-Tip: Most users find it best to split the 2.5 mg tablet into halves or quarters. A full 2.5 mg daily dose is usually too aggressive for anyone not dealing with a medical emergency.

The Risk of the Estrogen Crash

Crashing your estrogen too low with Letrozole can be as detrimental as having it too high. Estrogen is vital for joint health, libido, and brain function.⁴

• Joint Pain: Severe clicking or aching in the joints is the first sign of an estrogen crash.

• Bone Health: Long-term use of high-dose Letrozole can decrease bone mineral density (osteoporosis risk).⁵

• Lipid Impact: Excessive suppression can negatively affect cholesterol (LDL/HDL) ratios.

• Mental Health: Extremely low estrogen often leads to lethargy, depression, and a total loss of libido.

Frequently Asked Questions (FAQ)

1. Why is Letrozole considered the "strongest" AI?

In comparison to Anastrozole (Arimidex), Letrozole is approximately 10 to 30 times more potent.6 It provides a more complete inhibition of the aromatase enzyme, meaning it leaves almost no circulating estrogen in the body.

2. Can Letrozole actually reverse existing Gynecomastia?

Yes. While surgery is the only permanent cure for long-standing fibrotic tissue, Letrozole is highly effective at shrinking developing or "fresh" gynecomastia tissue. It is the most successful non-surgical intervention for athletes.

3. Should I use Letrozole for my PCT?

No. Letrozole is too aggressive for Post-Cycle Therapy. During PCT, your body needs a healthy amount of estrogen to recover its HPTA axis and protect your heart. SERMs like Nolvadex or Clomid are much better suited for recovery.

4. How do I know if I’ve taken too much?

If you experience dry, painful joints, sudden fatigue, or erectile dysfunction while taking Letrozole, you have likely crashed your estrogen. You should immediately reduce the dose or stop use for a few days to allow levels to normalize.

Clenomed 40 SYMPATHOMIMETIC AMINE Deus Medical

Active Substance: Clenbuterol Hydrochloride

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (40 mcg/tab)

Form: Oral

What Is Clenbuterol Hydrochloride (CLENOMED 40)?

CLENOMED 40 (Clenbuterol HCl) is not an anabolic steroid; it is a powerful stimulant that belongs to the classification of compounds known as sympathomimetics. It works by targeting the beta-2 adrenergic receptors in the body, stimulating the central nervous system (CNS) and accelerating the metabolic rate.¹

Clenbuterol is highly sought after for its dramatic use in fat loss, muscle gain preservation, cutting, and pre-contest cycles, delivering effects often described as "steroid-like" in terms of body composition changes.

Core Mechanisms and Benefits

• Accelerated Fat Loss (Thermogenesis): Clenbuterol increases the body’s core temperature, significantly boosting the Basal Metabolic Rate (BMR) and forcing the body to efficiently burn stored fat (lipolysis) for energy.

• Muscle Preservation: It helps to preserve lean muscle mass during caloric deficits, providing a distinct advantage over simple dieting.

• Enhanced Energy: It acts as a stimulant, increasing energy levels and allowing for more intense and sustained workouts.²

 Usage and Cycling Protocols (Titration is Mandatory)

Clenbuterol cycles require careful management due to the drug's effect on the CNS and the rapid development of receptor tolerance.

• Administration: Due to its long half-life of approximately 37 hours, the entire daily dosage should ideally be consumed at once in the morning to maximize effects while mitigating severe insomnia and sleep disturbances.

• Duration: It is recommended not to use Clenbuterol for more than 12 weeks total to give the cardiovascular system an adequate rest.

• Tolerance and Titration: The body quickly adapts to Clenbuterol. Users must slowly titrate (ramp up) the dosage to maintain effectiveness:

  • Initial Start: Begin with 40 mcg for the first 3 days.

  • Increase: On day 4, increase by 20 mcg (to a total of 60 mcg/day). Continue increasing by 20 mcg every 3 days thereafter.

• Peak Dosages: The maximum suggested dosage is generally 140 mcg per day for men and 80–120 mcg per day for women.

Cycle Types

1. 2 Weeks On / 2 Weeks Off: A common method to combat tolerance, allowing receptors to re-sensitize during the break.

2. Continuous Use (Up to 8 Weeks): Requires the use of a receptor sensitizer like Ketotifen every second week to prevent receptor downregulation.

 Side Effects and Safety Warning

As a powerful sympathomimetic, Clenbuterol's side effects are significant and primarily affect the heart and nervous system.³

• Common Side Effects: Tremors (shakiness), rapid heart rate, anxiety, insomnia, and restlessness.⁴

• Cardiovascular Risks: High doses and prolonged use can lead to serious cardiac issues, including hypertension and potential strain on the heart muscle.⁵

Crucial Warning: Consulting a healthcare professional before use is mandatory. Users must be fully aware of the cardiovascular risks and manage dosages responsibly.

 Frequently Asked Questions (FAQs)

1. Why does Clenbuterol require a specific "ramping up" and "weaning off" protocol?

Clenbuterol requires titration because the body's beta-2 receptors rapidly become desensitized (downregulated) to the compound.⁶ Ramping up ensures the body receives increasing stimulation to maintain the fat-burning effect. Weaning off (gradually decreasing the dose) is vital to allow the Central Nervous System (CNS) and heart rate to stabilize safely.

2. Can Clenbuterol be used during the "off-season" or bulking cycles?

Yes, although its primary use is for cutting, Clenbuterol can be beneficial during bulking. Its ability to preserve muscle mass and enhance endurance means it can help athletes gain cleaner mass and prevent excessive fat accumulation, effectively enhancing the "recomposition" effect.

3. If Clenbuterol is used during an anabolic cycle, does it still require Post Cycle Therapy (PCT)?

Clenbuterol itself is not a steroid and does not suppress natural testosterone production. Therefore, if run alone, it does not require PCT. However, since it is almost always stacked with anabolic steroids, the PCT protocol is mandatory to address the suppression caused by the co-administered steroids.

4. Why should the entire daily dose be taken in the morning?

Clenbuterol has a long half-life (around 37 hours).⁷ Spreading the dosage throughout the day would keep stimulating the CNS late into the evening, drastically increasing the severity of side effects like insomnia and anxiety. Taking the entire dose in the morning ensures peak levels occur during the day while allowing the compound's concentration to fall slightly by bedtime.

THYROMED 50 (Levothyroxine Sodium T4): Thyroid Hormone Support

Active Substance: Levothyroxine Sodium (T4, 50 mcg/tab)
Manufacturer: Deus Medical
Pack: 1 Box of 2x 25 Tablets (50 mcg per Tablet)
Form: Oral

What Is Levothyroxine Sodium (T4)?

Levothyroxine Sodium (THYROMED 50) is a synthetic version of Thyroxine (T4), the hormone naturally produced by the thyroid gland. It is classified as a thyroid agent and is the standard medication used to treat hypothyroidism (low thyroid hormone levels).  

T4 is largely considered the inactive precursor hormone. Once administered, the body converts it into the active hormone, Triiodothyronine (T3), which regulates the body's energy expenditure, metabolism, and protein synthesis.  

Core Functions and Mechanism

• Hormone Replacement: Replaces the hormone the thyroid gland normally produces, regulating energy and metabolism.  

• Metabolic Support: Once converted to T3, it increases the turnover of various endogenous macromolecules (protein, fat) by increasing their synthesis and degradation, affecting the overall metabolic rate.  

• Synergistic Stacking: T4 is often stacked with HGH (Human Growth Hormone) because thyroid hormones are essential for GH to potentiate bone growth and anabolic effects. HGH use can also sometimes suppress natural T4 to T3 conversion, making supplementation necessary.  

 Usage and Dosage Protocols (Stacking)

Levothyroxine dosing requires precision and must be done under medical guidance, especially when used outside of hormone replacement therapy.

• Replacement Dosage (General): The average adult maintenance dose for replacement is generally 100 mcg to 200 mcg daily, though starting doses are lower.

• Bodybuilding/Performance Misuse: Misuse dosages often fall in the range of 50 mcg to 200 mcg daily to support thyroid function and metabolism.

• Administration: Must be taken as a single daily dose, preferably on an empty stomach, 30 to 60 minutes before breakfast, as food and certain supplements can interfere with absorption.  

• Warning: The FDA warns that thyroid hormones should not be used for the treatment of obesity or for weight loss in euthyroid (normal thyroid function) patients.  

 Side Effects and Warnings (Overdosage Risk)

Side effects are primarily those of hyperthyroidism (T4 overdosage), which accelerates all bodily functions.  

• Cardiovascular Risks: Overdosing can cause serious, even life-threatening, manifestations of toxicity, including arrhythmias (abnormal heart rhythms), palpitations, increased pulse, and chest pain. The risk is higher in older patients.  

• Bone Density: Chronic overdosing with T4 can increase the risk of osteoporosis and fractures by increasing bone turnover.  

• Common Hyperthyroid Symptoms: Nervousness, anxiety, insomnia, tremors, heat intolerance, excessive sweating, increased appetite, and modest weight loss.  

• Precautions: Patients should never adjust their dose without medical guidance and should monitor for symptoms of hyperthyroidism.  

Frequently Asked Questions (FAQs)

1. What is the fundamental difference between T4 (Levothyroxine) and T3 (Cytomel)?

• T4 (Levothyroxine): Is the inactive precursor hormone. The body converts it into the active T3 as needed. It has a long half-life, providing smooth, stable hormone levels.  

• T3 (Cytomel): Is the active hormone that directly impacts metabolism. It has a short half-life and causes rapid metabolic spikes, often making it more potent for immediate fat loss but riskier.  

2. Why is T4 stacked with Growth Hormone (HGH)?

HGH use can sometimes suppress the natural conversion of T4 to T3 in the body, potentially leading to a mild hypothyroid state. Stacking T4 ensures adequate thyroid hormone levels are maintained, which is necessary for HGH to fully exert its anabolic and lipolytic effects.

3. Will taking T4 (Levothyroxine) cause significant weight loss in a healthy person?

No. In individuals with healthy thyroid function (euthyroid), doses of T4 within the normal physiological range are ineffective for weight reduction. The modest weight loss reported in hypothyroid patients is usually due to the loss of retained water when their hormone levels are corrected. T4 abuse for weight loss is dangerous due to severe cardiovascular risks.  

4. What is the proper way to take Levothyroxine Sodium?

It must be taken once daily, on an empty stomach, 30 to 60 minutes before breakfast. This timing is crucial because food, coffee, and certain supplements (like calcium or iron) can significantly impair the absorption of the T4 tablet, leading to unstable blood hormone levels.  

 DEUSTROPIN 4/12: Recombinant Human Growth Hormone (HGH)

Active Component: Recombinant Human Growth Hormone (rDNA origin)

Brand: DEUSTROPIN 4/12 (Deus Medical)

Concentration: 4 mg (12 IU) per Vial1

Pack: 1 Box of 10 Vials (120 IU total in box)

What Is Recombinant Human Growth Hormone (HGH)?

DEUSTROPIN is a pharmaceutical-grade form of Recombinant Human Growth Hormone (HGH), often referred to simply as Somatropin. HGH is a vital peptide hormone naturally produced by the pituitary gland.² It stimulates growth, cell reproduction, and regeneration in humans.³

When administered externally, HGH acts to enhance the body's natural processes, primarily through its powerful intermediary, Insulin-like Growth Factor 1 (IGF-1), which is synthesized in the liver.⁴

Core Performance Benefits

• Lipolysis (Fat Loss): HGH is a highly effective agent for promoting sustained fat loss by increasing lipolysis (the breakdown of fat stores) throughout the body.⁵

• Lean Muscle Development: It significantly promotes the growth of lean, high-quality muscle mass, often cited as being drier and denser than gains from traditional steroids.

• Collagen & Joint Health: HGH is renowned for strengthening connective tissues, tendons, ligaments, and cartilage.⁶ This provides excellent support for joints under heavy strain.

• Enhanced Recovery and Anti-Aging: Users experience vastly improved recovery rates, better sleep quality, increased skin elasticity, and an overall sense of enhanced vitality.

 Usage and Dosage Protocols

HGH requires specific dosing and cycle lengths to maximize benefits and ensure safety.⁷

• Therapeutic Dosage: For anti-aging or tissue repair, dosages are typically low, ranging from 1 to 3 IU daily.

• Performance Dosage: For bodybuilding and performance enhancement, dosages range from 4 IU to 10 IU daily. Dosages over 6 IU are often reserved for experienced users due to increased potential side effects.

• Administration: HGH is highly sensitive and must be injected subcutaneously (under the skin), typically in the morning or post-workout.

• Cycle Duration: HGH cycles are measured in months, not weeks. To see full benefits, HGH must be used for a minimum of 3–6 months. The most pronounced aesthetic benefits (fat loss, skin quality) usually appear after the 3rd or 4th month.

•  

 Side Effects and Management Essentials

Side effects from HGH are typically related to dosage and water retention.⁸

• Water Retention & Tingling: The most common side effect is water retention, especially in the extremities (hands, feet), which can cause numbness or tingling (carpal tunnel symptoms). This is generally manageable by reducing the dose or spacing it out.

• Insulin Sensitivity: Long-term, high-dose HGH use can potentially reduce insulin sensitivity (increase blood glucose), necessitating caution and potentially the use of stabilizing supplements.⁹

• Thyroid Function: HGH can potentially lower thyroid function (T3/T4) over time, sometimes requiring ancillary support (like low-dose T3).

 Frequently Asked Questions (FAQs)

1. Why is HGH measured in both mg and IU (International Units)?

HGH is a peptide hormone, and its potency is measured in International Units (IU), with $1 \text{ mg}$ of synthetic GH typically equaling $3 \text{ IU}$. The DEUSTROPIN 4/12 vial contains $4 \text{ mg}$ of active substance, which translates to $12 \text{ IU}$, making the total box content $120 \text{ IU}$ ($10 \text{ vials} \times 12 \text{ IU}$).

2. Should HGH be used alone or stacked with other compounds?

HGH is often stacked, as its mechanism works synergistically with other hormones.¹⁰ It is almost always stacked with Testosterone to amplify muscle growth, and sometimes with Insulin or T3 to maximize its anabolic and metabolic effects. HGH is effective when used alone but delivers maximal results in a well-planned stack.

3. Does HGH require Post Cycle Therapy (PCT)?

No. HGH is a peptide hormone that does not suppress the body's natural production of testosterone.¹¹ Therefore, standard PCT protocols using SERMs (like Nolvadex or Clomid) are not necessary after an HGH cycle. However, if HGH is stacked with an anabolic steroid, PCT is mandatory for the steroid component.

4. What is the best time of day to inject HGH?

There are two common protocols:

1. Morning Injection: Taking it in the morning (on an empty stomach) is preferred for maximizing its fat-burning (lipolytic) effects throughout the day.

2. Post-Workout Injection: Taking it immediately after a workout can maximize its recovery and muscle-building properties.

BPC-157 Deus Medical

Active Component: BPC-157 Pentadecapeptide (5 mg/vial)

Manufacturer: Deus Medical

Pack: 1 Vial x 5 mg

What Is BPC-157?

BPC-157, or "Body Protect Compound," is a naturally occurring peptide—a stable gastric pentadecapeptide—originally found in trace amounts within human gastric juices, where it serves to protect and heal the intestinal tract. When synthesized in a super-concentrated form, it demonstrates extremely high biological healing activity across various bodily systems.

Its long chemical name reflects its fifteen amino acid sequence, which remains stable even in harsh conditions, allowing it to exert anabolic healing effects in both the upper and lower GI tract.

Broad Spectrum Healing and Regeneration

Extensive research, largely conducted in rodent models since 1991, has shown BPC-157 to be remarkably effective in the repair and regeneration of numerous tissues with a favorable side effect profile.

Musculoskeletal and Connective Tissue Repair

• Tendon and Ligament Healing: It promotes the healing of tendons (e.g., Achilles tears) and ligaments (e.g., damaged medial collateral ligaments) by stimulating tendon growth, cell survival, and cell migration. It is shown to promote healing from tendon to bone.

• Muscle and Bone Repair: BPC-157 reverses systemic corticosteroid-damaged muscle healing and promotes bone healing in models with segmental defects.

• Wound Healing: It accelerates general wound healing and, through interaction with the Nitric Oxide (NO) system, promotes angiogenesis (new blood vessel formation).

Gastrointestinal and Anti-Inflammatory Effects

• GI Tract Protection: It provides powerful ulcer-preventive effects and repairs damage from inflammatory bowel disease (IBD) within days after administration.

• Painkiller Damage: It effectively eliminates the harmful effects of common painkillers on the gastrointestinal tract.

 Dosage and Administration (Research and Anecdotal)

While BPC-157 is widely researched, standardized human clinical doses are still being established.

• Research Dosage: Systematically effective doses are shown to range between 1–10 mcg per kilogram of body weight once a day, which usually translates to 200 mcg to 800 mcg total daily.

• Anecdotal Dosage: Many users report success with doses of 250–350 mcg twice a day, totaling 500–700 mcg daily.

 Status and Important Disclaimers

• Non-Patentable Status: Because BPC-157 is a natural peptide, it cannot be patented. This lack of financial incentive explains why it is not marketed to doctors and is not approved by the FDA as a drug for human use.

• Research Status: There have been no long-term human studies to date, and 90% of the studies originated from one initial Croatian clinical study.

• WADA/USADA Status: While some peptides are banned, BPC-157 is not currently listed as an illegal compound by organizations like WADA or USADA. Users should be aware that this status can change.

 Frequently Asked Questions (FAQs)

1. Why hasn't BPC-157 been approved by the FDA if the research shows such positive healing effects?

BPC-157 has not received FDA approval because it is a naturally occurring peptide and therefore cannot be patented. Without patent protection, major pharmaceutical companies lack the financial incentive to invest hundreds of millions of dollars into the mandatory, large-scale, long-term human clinical trials required for drug approval.

2. Is BPC-157 generally taken orally or via injection?

While BPC-157 is stable in gastric juice (making oral administration possible for GI tract issues), it is generally considered more systematically effective when injected (subcutaneously or intramuscularly). Injections deliver the super-concentrated peptide directly into the system or near the site of injury for maximum localized biological healing activity.

3. What is the difference between BPC-157 and BPC-157 Arg?

The difference lies in the formulation's stability. While BPC-157 is known as the stable gastric pentadecapeptide, the Arginine salt form (BPC-157 Arg) is a newer version designed for even greater stability and bioavailability, particularly in acidic environments or when stored as a powder.

4. What is the risk associated with BPC-157 promoting cell growth and healing?

The risk, though not fully established in human studies, lies in its ability to stimulate angiogenesis (new blood vessel formation) and cell growth. If an individual has undiagnosed or existing cancerous conditions, the component's regenerative action could theoretically promote the growth or spread of cancer cells. For this reason, anyone with a history of cancer should strictly avoid its use.

CJC-1295 DAC Deus Medical 

Active Component: Tetrasubstituted 30-Amino Acid Peptide Hormone (CJC-1295 DAC)14

Manufacturer: Deus Medical15

Pack: 1 Vial x 2 mg

Form: Injectable

What Is CJC-1295 DAC?

CJC-1295 DAC (Drug Affinity Complex) is an advanced, synthetic analog of Growth Hormone-Releasing Hormone (GHRH).¹⁶ It is a 30-amino acid peptide that acts by binding to receptors on the pituitary gland, stimulating the pulsatile release of the body's natural Human Growth Hormone (GH).¹⁷

The key feature of this compound is the DAC (Drug Affinity Complex) modification.¹⁸ This modification allows the peptide to permanently bind to plasma proteins (specifically albumin) in the bloodstream.¹⁹ This prevents rapid enzymatic degradation, extending its half-life significantly to approximately 6–8 days.²⁰

Core Performance Benefits

• Long-Lasting Effects: The extended half-life provides a stable and sustained elevation of Growth Hormone (GH) and Insulin-like Growth Factor 1 (IGF-1) levels for days after a single injection, drastically reducing injection frequency to 1–2 times per week.²¹

• Muscle Growth & Recovery: Elevated GH and IGF-1 are crucial for synthesizing new muscle tissue, accelerating post-workout recovery, and supporting healing.

• Body Composition Improvement: It supports fat loss by promoting lipolysis and assists with collagen synthesis for improved skin, tendon, and joint health.²²

• Preserved Pulsatility: Unlike injecting synthetic GH, CJC-1295 DAC preserves the natural, pulsatile secretion of GH, which is thought to be key for maximizing benefits while minimizing adverse effects.²³

Optimal Dosage and Usage

CJC-1295 DAC is administered infrequently due to its prolonged activity.²⁴

• Injection Frequency: Requires only 1–2 weekly injections (twice weekly is often considered ideal for maximum stable results).

• Clinical Dosage: Clinical studies suggest a dose range of $15-30 \text{ mcg/kg/week}$.

• Performance Dosage: Bodybuilders and athletes often use dosages in the range of $2000-5000 \text{ mcg weekly}$ (or $2 \text{ mg}$ to $5 \text{ mg}$ per week) for enhanced performance and physique development.

• Stacking: For the most dramatic effect, CJC-1295 DAC is typically stacked with a GHRP (Growth Hormone Releasing Peptide) such as Ipamorelin. The GHRP initiates the pulse, and the CJC-1295 DAC amplifies the magnitude of that pulse.

 Side Effects and Precautions

As a GH stimulator, CJC-1295 DAC can cause side effects associated with elevated GH/IGF-1 levels.²⁵ Always consult a healthcare professional before use.

• Common Side Effects: Temporary localized pain or irritation at the injection site, headache, light-headedness, and flushing.

• GH-Related Effects: Users may experience a tingling sensation (numbness) in the hands or feet, and mild water retention, especially during the initial phase of use.

 Frequently Asked Questions (FAQs)

1. What is the fundamental difference between CJC-1295 DAC and CJC-1295 without DAC?

The difference lies in the half-life.²⁶ CJC-1295 without DAC (Mod GRF 1-29) has a short half-life of only about 30 minutes, requiring multiple injections per day.²⁷ CJC-1295 DAC binds to albumin, extending its half-life to 6–8 days, thus allowing for a highly convenient weekly or twice-weekly injection schedule.²⁸

2. Does CJC-1295 DAC need to be stacked with another peptide for maximum effect?

Yes, stacking is highly recommended. CJC-1295 DAC (GHRH analog) enhances the size of the GH pulse. It is typically stacked with a GHRP (Growth Hormone Releasing Peptide like Ipamorelin or GHRP-6), which acts through a different receptor to initiate the pulse. Used together, they create a stronger, synergistic release of GH.

3. Does CJC-1295 DAC affect natural testosterone production, requiring PCT?

No, CJC-1295 DAC does not suppress the body's natural production of testosterone. It works by stimulating the pituitary gland to release the body's own GH.²⁹ Therefore, standard Post Cycle Therapy (PCT) protocols used for anabolic steroids are not required after a CJC-1295 DAC cycle.

GHRP-2: The Potent Growth Hormone Releasing Peptide

Active Component: Growth Hormone-Releasing Peptide 2 (GHRP-2)

Manufacturer: Deus Medical

Pack: 1 Vial x 10 mg

Form: Injectable

What Is GHRP-2?

GHRP-2 is a Growth Hormone Secretagogue (GHS), classified as a second-generation peptide.¹ It acts by binding to the ghrelin receptor in the pituitary gland and hypothalamus, stimulating a rapid and powerful pulse of the body's natural Human Growth Hormone (GH).²

GHRP-2 is highly valued for producing a more intense release of GH compared to first-generation peptides like GHRP-6, while generally being considered safer and less likely to cause side effects related to excessive hunger.

Core Functions and Benefits

• Intense GH Release: GHRP-2 is known for triggering a significant, sharp pulse of endogenous GH, which leads to heightened levels of the anabolic hormone IGF-1 (Insulin-like Growth Factor 1).

• Muscle Growth and Recovery: Elevated GH and IGF-1 levels enhance protein synthesis, leading to improved muscle growth, faster recovery from exercise, and stronger anti-aging effects.

• Minimal Hunger Effect: Unlike GHRP-6, which is known for dramatically increasing appetite due to stimulating gastric motility, GHRP-2 has less effect on hunger, making it easier to manage diet during cutting or recomp cycles.

• Cortisol/Prolactin Increase (Slight): While effective, GHRP-2 may slightly increase levels of Prolactin and Cortisol, which should be monitored, especially at higher doses.

 Usage and Dosage Protocols

GHRP-2 has a very short half-life and must be administered frequently to maintain elevated GH levels.

• Dosing Frequency: To maximize results, the saturation dose should be injected multiple times per day. The recommended protocol is 3–5 times a day.

• Saturation Dose: The calculated saturation dose is $1 \text{ mcg/kg}$ of body weight per injection.

• Standard Daily Dose: The common dose used is $100 \text{ mcg}$ per injection, totaling $300 \text{ mcg}$ to $500 \text{ mcg}$ per day.

• Administration: Typically injected subcutaneously (under the skin) on an empty stomach to avoid interference from high blood glucose levels.

 Side Effects

Side effects are generally mild but may include flushing, headache, and temporary irritation at the injection site. The primary hormonal side effects are:

• Prolactin and Cortisol: May slightly increase levels of Prolactin and Cortisol, which should be monitored, especially when stacking with other 19-nor compounds (like Trenbolone or Nandrolone).

• Tolerance: The pituitary gland's response can decrease over time, necessitating breaks or stacking with a GHRH analog (like CJC-1295).

 Frequently Asked Questions (FAQs)

1. What does it mean that GHRP-2 is a "Growth Hormone Secretagogue (GHS)"?

A GHS is a compound that stimulates the pituitary gland to release its stored Growth Hormone (GH), rather than being an external source of GH itself (like synthetic HGH). This results in a natural, pulsatile release of GH, which is often considered safer.

2. Is GHRP-2 used alone or stacked with another peptide?

GHRP-2 is most effectively stacked with a GHRH analog like CJC-1295 (DAC or non-DAC). The GHRP-2 initiates a large pulse of GH, and the GHRH analog amplifies the size of that pulse, resulting in a synergistic and much stronger total GH release.

3. Why is it important to inject GHRP-2 on an empty stomach?

GHRP-2's effectiveness is diminished by high levels of blood glucose. Injecting on an empty stomach (especially post-fasting, pre-meal, or post-workout) ensures that blood sugar levels are low, maximizing the peptide's ability to stimulate the pituitary gland and trigger the largest possible pulse of GH.

4. Does GHRP-2 suppress natural testosterone?

No. GHRP-2 is a peptide that targets the GH axis, not the HPTA (Hypothalamic-Pituitary-Testicular Axis). It does not suppress the body's natural production of testosterone. Therefore, GHRP-2 cycles do not require standard PCT protocols.

GHRP-6 Deus Medical

Active Component: Growth Hormone-Releasing Peptide 6 (GHRP-6)

Manufacturer: Deus Medical

Pack: 1 Vial x 10 mg

Form: Injectable

What Is GHRP-6?

GHRP-6 is a Growth Hormone Secretagogue (GHS), classified as a first-generation peptide.¹ It acts by binding to the ghrelin receptor, powerfully stimulating the pituitary gland to release a natural pulse of the body's Human Growth Hormone (GH).

GHRP-6 is particularly unique because, apart from releasing GH, it also significantly affects appetite and digestive function, making it an ideal choice for specific physique goals.

Core Functions and Benefits

• Intense Hunger Stimulation: GHRP-6 is well-known for its pronounced side effect of dramatically increasing appetite by improving gastric motility and stimulating ghrelin receptors. This is highly beneficial for athletes struggling to consume the necessary calories during a bulking or mass-gaining phase.

• Potent GH Release: It triggers a strong, rapid pulse of endogenous GH, which leads to heightened levels of the anabolic hormone IGF-1.

• Muscle Growth and Recovery: Elevated GH and IGF-1 levels enhance protein synthesis, leading to improved muscle growth, faster recovery from exercise, and support for joint health.

• Cortisol/Prolactin Increase (Slight): While highly effective, GHRP-6 may slightly increase levels of Prolactin and Cortisol, which must be managed, especially when stacking.

 Usage and Dosage Protocols

GHRP-6 has a very short half-life and must be administered frequently to maximize results.

• Dosing Frequency: To sustain elevated GH levels, injections must be frequent. The standard protocol is 3–5 times a day.

• Saturation Dose: The calculated saturation dose is $1 \text{ mcg/kg}$ of body weight per injection.

• Standard Daily Dose: The common dose used is $100 \text{ mcg}$ per injection, totaling $300 \text{ mcg}$ to $500 \text{ mcg}$ per day.

• Administration: Typically injected subcutaneously (under the skin) on an empty stomach (or before a meal) to maximize the GH release, as high blood sugar blunts its effect.

 Side Effects

Side effects are generally mild, but the intense hunger response is predictable.

• Increased Appetite: The most pronounced side effect is a significant and immediate increase in hunger, making it challenging for users in cutting cycles.

• Cortisol and Prolactin: May slightly increase levels of Prolactin and Cortisol. Management may be required, particularly if prolactin-sensitive components (like Trenbolone) are used.

Frequently Asked Questions (FAQs)

1. Is GHRP-6 better for bulking or cutting cycles?

GHRP-6 is generally preferred for bulking and off-season phases due to its intense effect on increasing appetite and improving gastric motility. For cutting cycles, where strict calorie control is essential, the hunger-stimulating effect of GHRP-6 can be counterproductive, and GHRP-2 (which is less hunger-inducing) is often preferred.

2. Why is the stacking of GHRP-6 with CJC-1295 so common?

Stacking GHRP-6 with a GHRH analog like CJC-1295 creates a synergistic effect. The GHRP-6 (like GHRP-2) initiates the natural GH pulse, and the GHRH analog amplifies the size of that pulse, resulting in a much stronger total release of Growth Hormone.

3. Why must GHRP-6 be injected so frequently (3-5 times a day)?

GHRP-6 has a very short half-life (around 15–30 minutes). To maintain a consistently elevated level of Growth Hormone throughout the day and maximize the anabolic window, it must be injected frequently, usually separated by 3–4 hour intervals.

4. Does GHRP-6 suppress natural testosterone?

No. GHRP-6 is a peptide that targets the pituitary gland's GH axis, not the HPTA (Hypothalamic-Pituitary-Testicular Axis). It does not suppress the body's natural production of testosterone. Therefore, GHRP-6 cycles do not require standard PCT protocols, though it is often stacked with steroids that do require PCT.

HCG 5000 Deus Medical 

HCG 5000 Deus Medical is a pharmaceutical preparation containing Human Chorionic Gonadotropin (HCG) in a strength of 5000 IU per vial. This hormone plays a crucial role in reproductive health and is widely used in medical treatments for hormone imbalance, fertility support, and specific pediatric conditions. Manufactured by Deus Medical, it is designed for clinical and therapeutic use under a doctor’s supervision.

What Is HCG 5000 Deus Medical?

HCG 5000 Deus Medical contains a high-purity form of Human Chorionic Gonadotropin, a hormone naturally produced during pregnancy. In medicine, it is used to support hormonal function in both men and women.

Manufacturer – Deus Medical

Deus Medical is known for:

• Pharmaceutical-grade hormone formulations

• Reliable packaging and labeling

• Strict compliance with quality standards

• QR-based authenticity verification

Product Format & Strength

• 1 vial per box

• 5000 IU (International Units)

• Sterile freeze-dried powder for reconstitution under medical guidance

Understanding Human Chorionic Gonadotropin (HCG)

Natural Role of HCG in the Human Body

HCG is produced by the placenta shortly after conception.
It is responsible for maintaining the early stages of pregnancy by supporting progesterone production. Because of its unique presence, pregnancy tests detect HCG levels in urine or blood.

Medical Classification

HCG acts similarly to Luteinizing Hormone (LH), a pituitary hormone that stimulates:

• Testosterone production in men

• Ovulation in women

This hormonal mimicry explains why HCG has powerful medical applications.

How HCG Works in the Human Body

Mimicking Luteinizing Hormone (LH)

Because HCG behaves like LH, it binds to the same receptors in the testes and ovaries.

In men:

• Stimulates Leydig cells

• Encourages natural testosterone production

In women:

• Supports follicle maturation

• Triggers ovulation

Testosterone Production Support

For men with clinically diagnosed hypogonadism, HCG helps restore normal hormonal function and reduce the consequences of low testosterone.

Medically Approved Uses of HCG

HCG is an FDA-approved medication with several important therapeutic uses.

Treatment of Male Hypogonadism

HCG assists men whose bodies cannot produce enough testosterone due to:

• Pituitary dysfunction

• Testicular underactivity

• Hormonal imbalance

Treatment of Undescended Testicles in Young Boys

HCG can stimulate testicular descent when medically appropriate.

Fertility Treatment in Women

Doctors use HCG to:

• Induce ovulation

• Support reproductive cycles

• Assist fertility protocols

Why HCG Is Clinically Important

Supporting Endocrine System Recovery

HCG helps re-activate hormonal pathways by stimulating testosterone production naturally.

Preventing Long-Term Hormone Suppression

Without proper hormonal support, low testosterone levels can affect:

• Muscle preservation

• Bone density

• Mood and energy

• Fertility

HCG helps restore natural endocrine activity under medical care.

Misconceptions About HCG

Not a Muscle-Building Drug

HCG does not directly improve muscle mass or athletic performance.

Not a Substitute for Testosterone Therapy

HCG supports hormonal pathways but does not replace clinical TRT when needed.

Side Effects and Safety Considerations

Common Side Effects

• Injection site redness

• Headache

• Fatigue

• Mood changes

Rare or Serious Side Effects

• Allergic reactions

• Gynecomastia (hormonal imbalance-related)

• Fluid retention

• Severe irritation at injection site

Immediate medical attention is required if severe symptoms appear.

Who Should NOT Use HCG 5000

Avoid use if you have:

• Prostate or breast cancer (men)

• Ovarian cysts (women)

• Thyroid or pituitary tumors

• Allergy to HCG

• Pregnancy-related disorders

Always consult a doctor before starting treatment.

Storage & Handling Instructions

• Store between 20–25°C (68–77°F)

• Protect from light

• Do not freeze

• Use only after proper reconstitution following medical instructions

Authenticity Verification for Deus Medical Products

Deus Medical products include a unique QR code on the packaging.
Scanning it verifies the product’s authenticity and protects users from counterfeit hormones.

FAQs About HCG 5000 Deus Medical

1. What is HCG 5000 Deus Medical used for?

It is used for medically supervised treatments such as male hypogonadism, fertility support in women, and pediatric management of undescended testicles.

2. Does HCG increase testosterone levels?

Yes—HCG mimics Luteinizing Hormone (LH), stimulating the testes to produce testosterone naturally.

3. Is HCG safe to use without a doctor?

No. HCG is a prescription hormone and must be used only under medical supervision due to hormonal risks and potential side effects.

HEXARELIN Deus Medical 2mg

Active Substance: Hexarelin (Growth Hormone-Releasing Peptide)

Manufacturer: Deus Medical

Pack: 1 Vial x 2 mg

Form: Injectable

What Is Hexarelin?

Hexarelin (also known as Examorelin) is a synthetic, peptidic compound classified as a Growth Hormone Secretagogue (GHS).¹ It exhibits a high affinity for the ghrelin/growth hormone secretagogue receptor (²$\text{GHSR}$) and is considered one of the most potent of all GHS peptides.³

Hexarelin is renowned for its ability to trigger the most intense release of Growth Hormone (GH) from the pituitary gland when compared to other GHRPs like GHRP-6 and GHRP-2.⁴

Core Functions and Unique Characteristics

• Maximum GH Release: Hexarelin provides the strongest stimulus for GH release among known $\text{GHRP}$s, leading to significant elevation of $\text{IGF-1}$ for muscle growth, recovery, and fat metabolism.

• Rapid Desensitization: Hexarelin's primary drawback is its tendency for rapid receptor desensitization.⁵ Studies show the GH response can be significantly blunted after just a few weeks of continuous use, necessitating a specific cycling protocol.

• Non-Selective Co-Release: Hexarelin causes a slight, dose-dependent rise in the release of other hormones, including Prolactin and Cortisol (ACTH).⁶ This requires careful monitoring and often necessitates ancillary support.

• Cardioprotective Properties: Research has also indicated that Hexarelin may possess cardioprotective properties by enhancing left ventricular function and reducing cell death (⁷$\text{apoptosis}$) in the heart muscle.⁸

 Usage and Dosage Protocols

Due to the rapid desensitization, Hexarelin cannot be used like other $\text{GHRP}$s and requires an intermittent dosing schedule.⁹

• Desensitization Protocol: To avoid receptor desensitization and maintain efficacy, Hexarelin must be used intermittently, typically every other day ($\text{EOD}$), allowing the $\text{GHSR}$ receptors to resensitize during the "off" day.

• Dosage: The recommended dose is $100 \text{ mcg}$ per injection, administered 3 times per day. This totals $300 \text{ mcg}$ on dosing days.

• Stacking Strategy: It is highly recommended to use Hexarelin on its $\text{EOD}$ schedule while filling the "off" days with another, less desensitizing $\text{GHRP}$ (such as Ipamorelin, GHRP-2, or GHRP-6) to maintain GH elevation without burning out the receptors.

• Stacking Synergy: Combining Hexarelin with a ¹⁰$\text{GHRH}$ analog (like ¹¹$\text{CJC}-1295$) results in a synergistic, massive GH pulse.¹²

 Side Effects and Management

Hexarelin's potency comes with a higher propensity for co-secretion of non-GH hormones.

• Prolactin and Cortisol: Hexarelin causes a slight, dose-dependent rise in both Prolactin and Cortisol.¹³ Prolonged elevation of Cortisol can cause anxiety and suppress the immune system, while elevated Prolactin can cause sexual dysfunction or gynecomastia.¹⁴

• Suppression: Like other $\text{GHRP}$s, it does not suppress natural testosterone but does suppress the body's natural GH production while it is being used.

 Frequently Asked Questions (FAQs)

1. Why does Hexarelin cause rapid receptor desensitization?

Hexarelin is the most potent $\text{GHRP}$, but this high potency leads to rapid saturation and subsequent downregulation of the ghrelin/$\text{GHSR}$ receptors. The receptors rapidly lose their sensitivity to the stimulus, requiring users to take breaks ($\text{EOD}$ use or cycling off) to allow the receptors to resensitize and the peptide to remain effective.

2. Is Hexarelin generally preferred over Ipamorelin or GHRP-2?

Hexarelin is generally preferred when the user is targeting the absolute highest possible peak GH release due to its superior potency. However, Ipamorelin or $\text{GHRP}-2$ are often preferred for long-term, daily use because they cause significantly less co-secretion of unwanted hormones like Prolactin and Cortisol.

3. Should Hexarelin be taken on an empty stomach?

Yes. Like all $\text{GHRP}$s, Hexarelin should be injected on an empty stomach (or before a meal) to maximize the GH pulse.¹⁵ High blood glucose and insulin levels can severely blunt the GH-releasing activity of the peptide, reducing its effectiveness.

4. What is the typical cycle duration for Hexarelin?

Due to its rapid desensitization, Hexarelin cycles are typically much shorter than those for other peptides. Users generally cycle Hexarelin for 4–6 weeks on, followed by a 2–4 week break to allow full receptor recovery.¹⁶ When used with the $\text{EOD}$ protocol, cycles can sometimes be extended, but continuous monitoring is necessary.

HGH FRAGMENT 176-191 Deus Medical

Active Component: Recombinant Human Growth Hormone Fragment 176-191

Manufacturer: Deus Medical

Pack: 1 Vial x 5 mg

What Is HGH Fragment 176-191?

HGH Fragment 176-191 is a modified, isolated part of the Human Growth Hormone (HGH) peptide chain.¹ This peptide is a fragment of the full HGH ²$191$ amino acid sequence.³ It is specifically engineered to contain the C-terminal amino acids ($176$ through $191$) that are known to be solely responsible for HGH's fat-regulating properties.

By isolating this specific fragment, researchers created a component that directly manages fat oxidation (fat burning) without promoting many of the side effects associated with full HGH use (such as potential insulin resistance).

Core Functions and Benefits

• Targeted Fat Oxidation: The primary function of the HGH Fragment ⁴$176-191$ is to stimulate lipolysis (the breakdown of stored fat) and inhibit lipogenesis (the creation of new fat), resulting in effective body fat reduction.⁵

• No Growth Promotion: Unlike full HGH, this fragment is designed to not stimulate IGF-1 production or cell proliferation, meaning it does not cause the bone or organ growth side effects (like acromegaly) linked to high-dose HGH.

• Blood Sugar Neutral: Studies show the fragment has little to no impact on blood glucose levels or insulin sensitivity, which is a key advantage over using full HGH.

• Enhanced Energy Expenditure: It promotes the oxidation of body fat, effectively increasing the body's energy expenditure.⁶

 Usage and Dosage Protocols

HGH Fragment $176-191$ requires frequent, divided injections for optimal fat-loss results.

• Recommended Dosage: Inject a total of $250 \text{ mcg}$ to $500 \text{ mcg}$ per day.

• Administration: The total daily dose should be divided into 3 or 4 injections. This is necessary because of the peptide's short half-life. Common timing is before breakfast, before training, and before bed.

• Duration: The peptide should be used for a minimum of three months to see substantial results.

 Frequently Asked Questions (FAQs)

1. Why must HGH Fragment $176-191$ be injected multiple times a day?

The HGH Fragment $176-191$ has a very short half-life (lasting only a few hours). Injecting the total daily dose into 3 or 4 smaller doses is essential to maintain elevated levels of the peptide in the bloodstream throughout the day. This provides continuous fat-burning signaling, maximizing its effectiveness.

2. Is this peptide legal in organized sports (WADA/USADA)?

No. HGH Fragment $176-191$ is categorized under "Peptide Hormones, Growth Factors, Related Substances, and Mimetics" by organizations like the World Anti-Doping Agency (WADA). Because it acts on the HGH axis to promote lipolysis, it is explicitly banned in competitive sports.

3. How does HGH Fragment $176-191$ compare to using full HGH for fat loss?

HGH Fragment $176-191$ is more selective for fat loss and is safer regarding insulin management. While full HGH promotes lipolysis, it also promotes cell growth and can negatively affect insulin sensitivity. The Fragment provides a targeted fat oxidation effect without the growth-promoting or diabetic risks associated with high-dose full HGH use.

4. Does this peptide require Post Cycle Therapy (PCT)?

No. HGH Fragment $176-191$ is a peptide and does not suppress the body's natural production of testosterone or other sex hormones. Therefore, standard PCT protocols using SERMs (like Nolvadex) or AIs are not required after using this peptide.

IPAMORELIN Deus Medical

Ipamorelin is a sophisticated pentapeptide recognized as a highly selective Growth Hormone Secretagogue (GHS) and a Ghrelin Receptor Agonist.¹ It functions by stimulating the pituitary gland to trigger a potent pulse of the body’s natural growth hormone (GH).² Often regarded as the premier selective secretagogue, it is prized for its ability to maximize GH release while minimizing the secretion of secondary hormones that typically cause unwanted side effects.³

Product Specifications

Core Functions and Superiority

• Selective GH Release: Unlike older generation secretagogues, Ipamorelin does not release significant volumes of Cortisol, Prolactin, Acetylcholine, or Aldosterone.⁴ This high selectivity results in a cleaner therapeutic profile.

• Anabolic Support: The resulting GH pulse elevates IGF-1 (Insulin-like Growth Factor 1) levels, which supports muscle development, metabolic fat loss, and enhanced systemic recovery.⁵

• Controlled Appetite: Ipamorelin provides a powerful GH pulse similar to GHRP-6 but without the intense hunger stimulation, allowing for better dietary control.⁶

• Recovery and Wellness: Increased GH levels contribute to improved sleep quality, joint health, and accelerated tissue repair.

Usage and Dosage Protocols

Ipamorelin possesses a relatively short half-life and is most effective when administered following specific protocols:

• Administration: The standard protocol involves a minimum of 200 mcg injected subcutaneously once daily, typically 5 out of 7 days per week.

• Frequency: Due to its short half-life, users often prefer multiple daily injections (2–3 times) to maintain elevated GH levels throughout the day.⁷

• Synergistic Stacking: It is highly recommended to combine Ipamorelin with a GHRH analog (such as CJC-1295).⁸ This combination acts on different receptors to generate a synergistic effect that can be up to five times more effective than using either peptide alone.⁹

Side Effects

Ipamorelin is known for its "clean" profile due to its high selectivity.¹⁰ It has minimal impact on Prolactin and Cortisol levels.¹¹ Potential minor side effects may include:

• Temporary flushing or headache.

• Mild irritation at the subcutaneous injection site.¹²

Frequently Asked Questions (FAQs)

1. Why is Ipamorelin considered the most selective GH Secretagogue?

It specifically targets the GH receptor without significantly increasing hormones like Cortisol and Prolactin.13 This prevents common issues associated with older peptides, such as water retention, aggression, or sexual dysfunction.

2. Is Ipamorelin effective on its own or must it be stacked?

While effective as a standalone treatment, stacking it with a GHRH analog is strongly recommended to amplify the pulse size.14 This dual-action approach maximizes the total growth hormone release.15

3. Does Ipamorelin require Post Cycle Therapy (PCT)?

No. Because it stimulates the natural GH axis rather than the testosterone-producing HPTA (Hypothalamic-Pituitary-Testicular Axis), it does not suppress natural testosterone production.

4. How does its effect on hunger compare to other peptides?

Ipamorelin has a significantly milder effect on appetite compared to GHRP-6. It allows users to gain the benefits of growth hormone without the immediate, intense hunger pangs often caused by increased gastric motility.16

GW501516 10 SARM Deus Medical

GW501516 by Deus Medical, widely known as Cardarine, is a research compound frequently categorized alongside SARMs, though it technically belongs to a class of drugs known as PPAR-Delta agonists.¹ It does not target androgen receptors; instead, it binds to receptors that regulate energy metabolism in the heart and skeletal muscles.

Cardarine is legendary for its ability to "reprogram" the body's fuel-burning preference. By switching the primary energy source from glucose to fatty acids, it offers unparalleled increases in cardiovascular endurance and fat loss, making it a favorite for endurance athletes and those in the "cutting" phase of their training.

Technical Product Specifications

Core Functions & Performance Effects

• Elite Endurance: Cardarine significantly increases the body's oxidative capacity.² Users report a dramatic "second wind" during cardio, allowing for longer, more intense training sessions with reduced recovery time.

• Rapid Fat Oxidation: It forces the body to burn stored fat for energy rather than breaking down carbohydrates or muscle tissue.³ This results in a potent fat-burning effect while sparing lean muscle mass.

• Glycogen Sparing: By utilizing fatty acids for fuel, the body preserves its glucose stores. This is particularly beneficial for high-intensity training where glycogen depletion usually leads to "hitting the wall."

• Metabolic Health: Clinical research showed that Cardarine could improve insulin sensitivity and help balance cholesterol levels (HDL/LDL), though its development for these purposes was halted.

• Zero Suppression: Because it is not a hormone, Cardarine does not interfere with natural testosterone production.

Usage & Dosage (Research-Based)

Cardarine is typically used in cycles to maximize performance and metabolic efficiency.

Pro-Tip: Many athletes start at 10 mg for the first few weeks to assess their cardiovascular response before increasing to the full 20 mg dose.

Critical Safety Warning

It is vital to acknowledge that clinical development of GW501516 was stopped in 2007.⁴ During long-term, high-dose animal studies, researchers observed the rapid development of cancer in several organs. While the human equivalent of those doses is debated, WADA and USADA have issued public warnings regarding its safety.⁵ Users should approach this compound with full awareness of its research status and potential risks.

Frequently Asked Questions (FAQ)

1. Is Cardarine a SARM?

No. It is often sold as a SARM for marketing purposes, but it does not affect the androgen receptor. It is a PPAR-Delta agonist. This means it will not cause virilization in women or shut down testosterone in men.

2. Can I stack Cardarine with SARMs or Steroids?

Yes. Cardarine is frequently stacked with SARMs like Ostarine for a dry cutting cycle or with Trenbolone to help mitigate the cardiovascular "wind" issues often associated with that steroid.6

3. Does Cardarine require a PCT?

No. Since it does not affect your natural hormone production or suppress testosterone, no Post-Cycle Therapy (PCT) is required. You can stop usage without needing recovery medications like Clomid or Nolvadex.

4. How fast does it start working?

The endurance benefits are often felt within the very first few doses. Most users notice they can run further or train harder within the first 48–72 hours of starting a 10 mg daily dose.

LGD4033 10 SARM Deus Medical

Active Substance: LGD4033 (Also known as Ligandrol, VK5211)1

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets ($10 \text{ mg}$ per Tablet)

Form: Oral

What Is LGD4033 (Ligandrol)?

LGD4033 is a novel, non-steroidal compound belonging to the class of Selective Androgen Receptor Modulators (SARMs).² It is currently an investigational drug, originally developed to treat muscle wasting associated with conditions like aging, cancer, and hip fracture recovery.³

Ligandrol is known for binding to the androgen receptor (⁴$\text{AR}$) with high affinity and selectivity.⁵ Its powerful anabolic effects on muscle and bone are comparable to traditional steroids, but it shows robust selectivity for muscle tissue over androgen-sensitive organs like the prostate gland.⁶

Core Performance Benefits

• Potent Anabolic Activity: LGD4033 has been reported to possess some of the highest anabolic capabilities of any known SARM.⁷ Clinical trials have shown it can increase lean body mass (LBM) in a dose-dependent manner, even during short cycles.⁸

• Tissue Selectivity: It acts as a partial agonist on the ⁹$\text{AR}$ in the prostate and sebaceous glands, while acting as a full agonist in muscle and bone.¹⁰ This selectivity is the theory behind its potential to build muscle and bone mass with a reduced risk of androgenic side effects like prostate enlargement.¹¹

• High Oral Bioavailability: As an oral compound, LGD4033 has a long elimination half-life, allowing for convenient once-daily dosing.¹²

• Strength and Recovery: It effectively stimulates protein synthesis and is used by athletes to gain solid muscle mass, increase strength, and enhance athletic performance.¹³

 Usage and Dosage Protocols

LGD4033 is an investigational drug, and its use outside of clinical trials is banned and ill-advised. Black market dosages often exceed research levels.

• Clinical Dose: Clinical trials used very low doses (e.g., ¹⁴$0.1 \text{ mg}$ to ¹⁵$1.0 \text{ mg}$ daily) to assess safety.¹⁶

• Common Abuse Dose (Black Market): Athletes typically misuse $5 \text{ mg}$ to $20 \text{ mg}$ per day, with $10 \text{ mg}$ being a common intermediate dose.

• Duration: Cycles typically last between 8 to 12 weeks.¹⁷

• Storage: Store below $30^\circ\text{C}$. Protect from light. Do not freeze.

 Side Effects and Hormonal Suppression

Although SARMs are marketed as "safer," LGD4033 is associated with significant, dose-dependent side effects.¹⁸

• Severe Hormonal Suppression (Guaranteed): LGD4033 causes a dose-dependent suppression of total testosterone, sex hormone-binding globulin (¹⁹$\text{SHBG}$), and free testosterone.²⁰ This requires a mandatory Post Cycle Therapy (PCT) protocol.²¹ Hormone levels typically return to baseline after treatment discontinuation.²²

• Adverse Lipid Changes: It significantly decreases ²³$\text{HDL}$ cholesterol (good cholesterol) and increases triglycerides, which could theoretically increase the risk of heart attack and stroke.²⁴

• Liver Concerns: Case reports suggest a risk of drug-induced liver injury (²⁵$\text{DILI}$) and elevated liver enzymes (²⁶$\text{ALT}$ and ²⁷$\text{AST}$), especially at high doses or with prolonged use.²⁸

• WADA Prohibition: LGD4033 is on the World Anti-Doping Agency (²⁹$\text{WADA}$) Prohibited List due to its potential for performance enhancement and is illegal in sports.³⁰

 Frequently Asked Questions (FAQs)

1. Does LGD4033 require a Post Cycle Therapy (PCT)?

Yes, absolutely. The first human clinical trials confirmed that LGD4033 causes dose-dependent suppression of natural testosterone and ³¹$\text{SHBG}$.³² Even though hormone levels typically return to baseline after cessation, a proper PCT protocol using SERMs (Nolvadex or Clomid) is necessary to accelerate recovery and prevent the symptoms of low testosterone.

2. How does LGD4033 compare to Ostarine (MK-2866) in terms of potency?

LGD4033 is generally considered to be more potent and anabolic than Ostarine. LGD4033 is typically favored for bulking and significant mass gain, whereas Ostarine is preferred for cutting, joint support, and maintaining mass on a caloric deficit.

3. Is LGD4033 liver toxic?

While not as hepatotoxic as oral ³³$17\alpha$-alkylated steroids (like Dianabol), LGD4033 is an oral compound that can cause liver strain.³⁴ Clinical trials noted elevated liver enzymes, and there are case reports of severe Drug-Induced Liver Injury (³⁵$\text{DILI}$) associated with its misuse, particularly at high doses and long durations.³⁶ Liver enzyme monitoring is advised.

4. Why is LGD4033 often marketed as having "reduced side effects" on the prostate?

The claim stems from animal studies showing its tissue selectivity: LGD4033 demonstrated potent anabolic activity in muscle and bone but weaker (partial agonist) activity in the prostate gland compared to traditional steroids.³⁷ The theory is that this selectivity avoids unwanted prostate enlargement, though long-term human safety remains unestablished.

What is MK2866 10 SARM Deus Medical?

MK2866 10 mg/tab

1 Box of 2x 25 Tablets, 10mg per Tablet

Store below 30°C.

Protect from light. Do not freeze.

MK677 10 SARM Deus Medical

MK-677 by Deus Medical, widely known as Ibutamoren, is a potent, non-peptide growth hormone secretagogue.¹ Although frequently grouped with SARMs, MK-677 belongs to a different class of compounds. It functions by mimicking the hormone ghrelin and binding to ghrelin receptors in the brain, which triggers the pituitary gland to release significant pulses of natural Growth Hormone (GH) and Insulin-like Growth Factor 1 (IGF-1).²

Because it is orally active and does not require injections, MK-677 is the premier choice for athletes seeking the benefits of elevated GH—such as improved recovery, fat loss, and skin quality—without the cost or hassle of synthetic HGH.

Technical Product Specifications

Core Performance & Metabolic Benefits

• Elevated HGH & IGF-1: MK-677 provides a sustained increase in growth hormone levels, which leads to a downstream rise in IGF-1.³ This creates a powerful environment for tissue repair and cellular regeneration.⁴

• Rapid Recovery: Users report significantly faster healing of muscles, tendons, and ligaments, making it an excellent tool for training longevity.

• Improved Sleep Architecture: One of the most immediate benefits is a dramatic improvement in REM (Rapid Eye Movement) sleep quality, leading to better cognitive function and physical restoration.⁵

• Lean Mass Preservation: MK-677 is highly anti-catabolic.⁶ It helps protect muscle tissue even during calorie-restricted phases, ensuring you lose fat rather than muscle.

• Skin, Hair, and Nails: Elevated GH levels improve collagen production, often resulting in clearer skin, faster-growing nails, and healthier hair.

Usage & Dosage Protocols

Unlike many peptides, MK-677 has a long half-life (approx. 24 hours), allowing for convenient once-daily dosing.⁷

Pro-Tip: Because MK-677 can increase hunger significantly, most users taking it for fat loss prefer to dose it before bed to "sleep through" the initial hunger spike.

Side Effects & Management

• Increased Appetite: A primary effect of ghrelin mimetics.⁸ This is a benefit for those "hard gainers" but requires discipline during a cutting phase.

• Water Retention: Some users experience mild edema (swelling) in the hands and feet.⁹ Reducing sodium intake can help mitigate this.

• Insulin Sensitivity: Long-term use of GH secretagogues can elevate blood sugar.¹⁰ Monitoring fasting glucose and taking periodic breaks (e.g., 5 days on, 2 days off) is a common strategy.

• Lethargy: Some users report feeling tired during the day.¹¹ Adjusting the dosage to nighttime usually resolves this.

• Non-Suppressive: MK-677 does not affect natural testosterone production and does not require a PCT.

Frequently Asked Questions (FAQ)

1. Is MK-677 a SARM?

Technically, no. SARMs target the androgen receptor.12 MK-677 targets the ghrelin receptor to stimulate growth hormone.13 It does not cause hormonal suppression or virilization.

2. Can I stack it with SARMs or Steroids?

Yes. MK-677 is one of the most versatile compounds and is frequently stacked with LGD-4033 or RAD-140 to enhance recovery and "fill out" the muscle with more water and nutrients.

3. Does it cause "Bubble Gut"?

No. The "GH Gut" seen in professional bodybuilders is usually the result of extremely high doses of synthetic HGH combined with insulin. MK-677 stimulates your own natural pulses, which stay within a much safer physiological range.

4. How long does it take to see results?

Sleep and appetite changes happen within the first 48 hours. The cosmetic changes (skin, muscle fullness) and recovery benefits typically manifest after 4 to 6 weeks of consistent use.

RAD140 (Testolone): The Highly Potent, Non-Steroidal SARM

Active Substance: RAD140 (Also known as Testolone)

Manufacturer: Deus Medical

Pack: 1 Box of 2x 25 Tablets (10\mg/tab)

Form: Oral (Tablet)

What Is RAD140 (Testolone)?

RAD140 is a novel, non-steroidal compound belonging to the class of Selective Androgen Receptor Modulators (SARMs).² It is an investigational drug developed to exhibit potent anabolic effects on muscle and bone tissue without causing the unwanted androgenic side effects associated with traditional anabolic steroids (AAS).

Research suggests RAD140 has one of the highest anabolic-to-androgenic ratios of all SARMs discovered to date, offering anabolic potency greater than Testosterone itself, based on preclinical models.

Core Performance Benefits

• Extreme Anabolic Potency: RAD140 is highly effective at stimulating lean body mass (LBM) increases and dramatic strength gains, making it a popular choice for bulking and strength-focused cycles.

• High Tissue Selectivity: It binds with high affinity to the androgen receptors AR in muscle and bone.⁴ The goal of this selectivity is to maximize muscle growth while minimizing androgenic effects in sensitive tissues like the prostate.

• Neuroprotective Effects: Preclinical data suggests RAD140 may possess neuroprotective properties, potentially protecting brain cells from damage (e.g., amyloid-beta toxicity, similar to the action of Testosterone).⁵

• Non-Aromatizing: RAD140 is non-steroidal and cannot aromatize (convert) into estrogen.⁶ This eliminates the risk of estrogen-related side effects like water retention and gynecomastia.

Usage and Dosage Protocols

RAD140 is an investigational drug, and its use outside of clinical trials is banned and ill-advised.⁷ Black market dosages often exceed research levels.

• Typical Dose (Black Market Misuse): Athletes typically misuse $10\mg to 30mg per day, with 10mg being a common starting and therapeutic dose.

• Duration: Cycles typically last between 8 to 12 weeks.

• Administration: Due to its half-life, RAD140 is generally taken once daily.

• Storage: Store below 30. Protect from light. Do not freeze.

Side Effects and Hormonal Suppression

Although selective, RAD140 is potent enough to cause significant hormonal side effects.

• Severe Hormonal Suppression (Guaranteed): RAD140 causes severe suppression of natural testosterone production. This requires a mandatory Post Cycle Therapy (PCT) protocol using SERMs (Nolvadex or Clomid) to accelerate the recovery of the Hypothalamic-Pituitary-Testicular Axis.

• Androgenic Effects: Despite its selectivity, some users report androgenic side effects like acne and accelerated hair loss (in genetically predisposed individuals) due to its overall high potency.

• Hepatotoxicity: Some case reports suggest a risk of elevated liver enzymes  and, necessitating caution and potential monitoring.¹⁰

• WADA Prohibition: RAD140 is explicitly on the World Anti-Doping Agency WADA) Prohibited List due to its potent performance-enhancing capabilities.¹²

 Frequently Asked Questions (FAQs)

1. Does RAD140 require a Post Cycle Therapy (PCT)?

Yes, absolutely. Unlike earlier SARMs, RAD140 is potent enough to cause severe suppression of the body's natural testosterone production. A comprehensive PCT protocol using SERMs (like Nolvadex or Clomid) is mandatory after every cycle to prevent the symptoms of low testosterone and ensure the

{HPTA} recovers fully.

2. How does RAD140 compare to LGD4033 in terms of potency?

Both are highly potent SARMs favored for bulking. While LGD4033 is often preferred for overall mass gain, RAD140 is generally considered to possess a slightly higher anabolic ratio and is favored for raw strength and hardness gains, though the overall effects are quite similar.

3. Will RAD140 cause gynecomastia or water retention?

No. RAD140 is non-steroidal and cannot aromatize (convert) into estrogen.¹³ Therefore, it does not cause estrogen-related side effects like water retention or gynecomastia. If gyno occurs during a RAD140 cycle, it is usually due to the user's natural testosterone production being suppressed, leading to an imbalance where existing estrogen becomes dominant.

4. Is RAD140 toxic to the liver?

As an oral compound, RAD140 is metabolized by the liver, and there are case reports linking its use to elevated liver enzymes {ALT/AST} and potential liver injury, especially at high doses.¹⁵ While not as acutely toxic as alpha-alkylated steroids (like Dianabol), liver monitoring is necessary.¹⁷

S23 10 SARM Deus Medical

Type and Article: S-23 (Selective Androgen Receptor Modulator)

S-23 belongs to a class of compounds called Selective Androgen Receptor Modulators (SARMs).²

• Mechanism: SARMs are non-steroidal compounds designed to selectively stimulate androgen (sex hormone) receptors in certain tissues, such as muscle and bone, while minimizing the effects on other tissues like the prostate.³

• Original Development: S-23 was initially developed by a company called GTX, Inc.⁴ and was primarily investigated as a potential male hormonal contraceptive due to its ability to suppress sperm production (spermatogenesis) in animal models, with effects that were shown to be reversible upon cessation of treatment.⁵

 Why Bodybuilders Use S-23

Despite its investigational status, S-23 is used by some in the bodybuilding and athletic communities because it is often purported to:

1. Increase Muscle Mass and Strength: Like other SARMs, users seek S-23 for its strong anabolic effects, hoping to stimulate rapid muscle growth similar to anabolic steroids but with potentially fewer side effects in non-target tissues.

2. Increase Bone Density: Animal studies have suggested S-23 can increase bone mineral density.⁶

3. Reduce Fat Mass: Research in rats showed that S-23 could reduce body fat in a dose-dependent manner.⁷

4. Cutting/Hardening Agent: It is rumored to be one of the most potent SARMs, often used during "cutting" cycles (periods of fat loss) to retain muscle mass and achieve a "harder," more defined physique.

Note: S-23, like all SARMs, is banned by the World Anti-Doping Agency (WADA) and various athletic organizations due to its performance-enhancing effects.⁸

 What Are the Side Effects?

Since S-23 has not undergone full-scale human clinical trials and is not FDA-approved, the full scope of its risks and long-term side effects is unknown. However, preliminary research and warnings from health authorities like the FDA have associated SARMs, including S-23, with serious health risks:⁹

Common/Reported Side Effects:

• Testosterone Suppression: S-23 is known for causing significant and dose-dependent suppression of natural testosterone levels (HPTA axis), which is the intended mechanism for its contraceptive potential.¹⁰ This often requires a Post-Cycle Therapy (PCT) to help restore natural hormone production.

• Testicular Atrophy: As a consequence of hormonal suppression, testicular shrinkage may occur.¹¹

• Infertility: The contraceptive effect involves suppressing spermatogenesis, leading to temporary infertility that may or may not be fully reversible.

• Aggression and Mood Swings (Anabolic/Androgenic effects).

Serious Health Risks (FDA Warnings):

• Liver Injury/Acute Liver Failure: Severe harm to the liver has been associated with SARM use.¹²

• Increased Risk of Heart Attack or Stroke: Cardiovascular complications are a major concern.¹³

• Psychosis and Hallucinations.¹⁴

• Sleep Disturbances.¹⁵

• Sexual Dysfunction.

❓ 4 Frequently Asked Questions (FAQ)

1. Is S-23 legal to buy?

S-23 is generally sold as a "research chemical" and is not approved for human consumption. While the chemical itself may not be scheduled, selling it for human use as a dietary supplement or drug is illegal according to the FDA. The FDA has issued warnings and taken legal action against companies selling products containing SARMs.¹⁶

2. Is S-23 considered a steroid?

No. S-23 is a Selective Androgen Receptor Modulator (SARM).¹⁷ It is a non-steroidal compound.¹⁸ While it mimics some of the anabolic effects of traditional anabolic-androgenic steroids (AAS) by activating androgen receptors, its chemical structure is different and it is designed to be more selective, although this selectivity is not guaranteed in practice.

3. What is the recommended dosage for S-23?

There is no medically established or safe recommended dosage for S-23 because it is an investigational drug, not a prescribed medication or approved supplement. Dosages found on bodybuilding forums are anecdotal and can be extremely unsafe, potentially leading to severe side effects.

4. How long do the suppressive effects of S-23 last?

Because S-23 is highly suppressive of natural testosterone, the effects on the body's hormonal system will persist after the cycle is completed. While studies in animals suggest reversibility, the time it takes for a user's natural hormone levels to fully recover can vary greatly. Many users require a Post-Cycle Therapy (PCT) protocol to attempt to expedite the recovery of their natural testosterone production.

YK 11 Deus Medical

Active Component: YK11

Brand: YK11 (Deus Medical)

Pack: Oral Tablets (5 mg/tab)

Form: Oral

Product Overview: What Is YK11?

YK11 is a powerful component that is often classified as a SARM (Selective Androgen Receptor Modulator), but its mechanism is structurally and functionally unique.¹ It acts as a gene-specific partial activator of Androgen Receptors (AR).

However, its most notable function is its role as a Myostatin Inhibitor. By stimulating the body to produce Follistatin—a protein that actively blocks Myostatin (a protein that naturally limits muscle growth)—YK11 is designed to promote muscle growth far beyond a user's genetic limitations.²

How YK11 Works (Unique Mechanism)

YK11's action is twofold:

1. Androgen Receptor (AR) Activation: It partially stimulates ARs to promote anabolic effects (muscle and bone growth).³

2. Myostatin Inhibition: Its key mechanism is promoting the synthesis of Follistatin.⁴ By inhibiting the growth-limiting protein Myostatin, YK11 effectively lifts the "genetic brake" on muscle development, leading to potential enhanced muscle growth and strength gains beyond what is typically possible with traditional anabolics alone.⁵

 Recommended Dosage

YK11 is a potent research compound, and only low dosages are suggested.

• Suggested Dosage: 5 mg daily, taken orally.

• Administration: Typically taken once per day.

 Potential Side Effects and Safety Warning

Due to its potent nature and complex mechanism, YK11 carries significant potential side effects. Its status as a research chemical means long-term human safety data is scarce.⁶

Crucial Warning: YK11 is a research compound and is not approved for human consumption. Due to potential risks, including severe liver damage and cancer risk with overuse, extreme caution and medical guidance are paramount before considering its use.

Please provide the article you would like me to add 4 FAQs to.

(If you meant the last article, YK11, here are 4 FAQs based on that content):

Frequently Asked Questions (FAQs) about YK11

1. What makes YK11 different from traditional SARMs (Selective Androgen Receptor Modulators)?

YK11 is unique because it acts not only as a partial androgen receptor activator but primarily as a Myostatin Inhibitor. Myostatin is a protein that naturally limits muscle growth. By stimulating the production of Follistatin, YK11 blocks Myostatin, potentially allowing muscle growth to exceed natural genetic limits, a mechanism not seen in traditional SARMs like Ostarine or LGD-4033.

2. If YK11 is a SARM, why is liver damage a potential side effect?

Like many oral compounds, YK11 may place stress on the liver. Although SARMs are designed to be more selective than traditional oral steroids, the product information specifically cautions about the potential for liver damage and the risk of cancer with overuse. This highlights the fact that YK11 is a powerful research chemical and is not without significant systemic risk.

3. Why is the risk of "Testosterone Suppression" mentioned if YK11 is a partial activator?

While YK11 partially activates androgen receptors, the body recognizes its presence as an exogenous (external) hormone, signaling the HPTA (Hypothalamic-Pituitary-Testicular Axis) to reduce or stop its own natural testosterone production. Therefore, just like with full steroids, users should anticipate and plan for testosterone suppression and require a proper Post Cycle Therapy (PCT) protocol.

4. Given its potent mechanism, why is the suggested dosage only 5 mg daily?

The low suggested dosage of 5 mg is indicative of YK11's extreme potency and its direct action on gene expression and protein synthesis (Myostatin inhibition). At higher doses, the risk of severe side effects—including liver damage, anxiety, and potential cardiac issues—increases dramatically, making a low, tightly controlled dosage the only viable research path.

SR9009 (Stenabolic): The Metabolic and Endurance Enhancer

Active Substance: SR9009 (Stenabolic)
Manufacturer: Deus Medical
Pack: 50 Tablets in Container (10 mg/capsule)
Form: Oral (Capsule/Tablet)

What Is SR9009 (Stenabolic)?

SR9009, commonly known as Stenabolic, is a potent research drug that is often mistakenly classified as a SARM (Selective Androgen Receptor Modulator). It is, in fact, an agonist of the REV-ERBα/REV-ERBβ nuclear receptors.  

Originally developed by Professor Thomas Burris to study the body's circadian rhythm, SR9009 influences the body's biological clock and metabolism, leading to effects that mimic the benefits of exercise. For this reason, it is classified as a Hormone and Metabolic Modulator by the World Anti-Doping Agency (WADA).  

Core Functions and Mechanism

SR9009 works by activating the REV-ERB receptors, which play a pivotal role in regulating cellular energy.  

• Mitochondrial Biogenesis: SR9009 increases the number and efficiency of mitochondria (the cell's powerhouses) in skeletal muscle. This results in higher energy output and reduced fatigue.  

• Enhanced Energy Expenditure: By activating REV-ERBα, it alters the circadian pattern of metabolic genes in the liver and skeletal muscle, increasing overall energy expenditure and raising the Basal Metabolic Rate (BMR), even at rest.  

• Fatty Acid Oxidation: It enhances the metabolism of both fatty acids and glucose, promoting a switch to fat burning and accelerating fat loss.  

• Endurance Boost: Studies in animal models showed SR9009 significantly increased exercise capacity, leading to its illicit use by athletes for its potent ergogenic effects.  

 Usage and Dosage Protocols

Due to its short half-life, SR9009 requires strict, multiple-daily dosing to maintain stable levels, despite its oral form.  

• Recommended Dosage: The generally recommended dosage for misuse ranges between 10 mg to 30 mg per day. Beginners are advised to start at 10 mg per day.  

• Administration Frequency: Due to a relatively short half-life, SR9009 requires multiple daily doses to maintain stable plasma levels. A common protocol is to divide the total daily intake into two to three equal doses, taken approximately every 4 to 6 hours.  

• Cycling Protocol: To prevent the development of tolerance, cycles typically range from 8 to 12 weeks, followed by a minimum 4-week break.  

 Side Effects and Warnings

SR9009 is an investigational drug, and its long-term safety profile in humans is unknown.

• Circadian Rhythm Interference: Because SR9009 directly influences the body's clock, one of the most common user-reported side effects is disrupted sleep, increased wakefulness, and insomnia.  

• Anecdotal Effects: Other reported side effects include nausea and headache.  

• WADA Prohibition: SR9009 is explicitly placed on the World Anti-Doping Agency (WADA) Prohibited List under the category of Hormone and Metabolic Modulators due to its potent ergogenic effects on endurance.  

 Frequently Asked Questions (FAQs)

1. Why must SR9009 be taken multiple times per day despite being a capsule?

SR9009 has a very short half-life (approximately 4 hours). Although it is an oral capsule, it is cleared from the body quickly. To maintain stable activation of the REV-ERB receptors and sustain the metabolic and endurance-boosting effects throughout the day, the total dose must be split into 2-3 administrations.

2. Is SR9009 a SARM or a Metabolic Modulator?

SR9009 is a Metabolic Modulator, specifically a REV-ERBα agonist. It is often falsely advertised as a SARM on the black market, but it does not bind to the androgen receptor. It modulates metabolism, endurance, and fat burning primarily through its effect on mitochondrial function and the circadian clock.  

3. Does SR9009 suppress natural testosterone production?

No. Since SR9009 does not bind to the androgen receptor (AR), it does not interfere with the HPTA (Hypothalamic-Pituitary-Testicular Axis). Therefore, SR9009 cycles do not require standard Post Cycle Therapy (PCT) protocols using SERMs (like Nolvadex or Clomid).

4. What is the primary safety risk associated with SR9009?

The primary user-reported risks are related to disrupted sleep and circadian rhythm interference due to its REV-ERBα mechanism. As a research chemical not FDA-approved, the long-term systemic risks in humans are completely unknown, and it should be approached with extreme caution.  

 S4 25 Andarine SARM Deus Medical: A Complete Guide

Type and Article: Andarine (S-4)

Andarine (S-4) is one of the earliest developed Selective Androgen Receptor Modulators (SARMs).¹

• Original Development: It was developed by GTX, Inc.² for treating conditions like muscle wasting (cachexia), osteoporosis, and benign prostatic hyperplasia (BPH).³

• Mechanism: S-4 acts as a partial agonist of the androgen receptor (AR). In certain tissues (like muscle and bone), it activates the receptor, promoting anabolic effects.⁴ In other androgenic tissues (like the prostate), it acts as a partial agonist/competitive antagonist, which theoretically limits the unwanted androgenic side effects seen with traditional anabolic steroids.⁵

• Discontinued Status: Clinical trials for Andarine were discontinued, reportedly due to findings of visual disturbances in human studies.

 Why Bodybuilders Use Andarine (S-4)

Bodybuilders and athletes use Andarine primarily for its reputation as an effective agent for:

• Muscle Mass Maintenance: It is often used during "cutting" cycles where the goal is to lose body fat while strictly preserving existing lean muscle mass.

• Increased Muscle Hardness/Definition: Users report a "hardening" effect on the muscles, giving a more defined and vascular appearance.

• Moderate Anabolic Effects: Compared to other SARMs like LGD-4033 or RAD-140, its anabolic effects are considered more mild, but its partial agonist nature is thought to confer greater tissue selectivity.

Note: Andarine (S-4) is on the World Anti-Doping Agency (WADA) Prohibited List and is banned in competitive sports.

What Are the Side Effects?

The full safety profile and long-term effects of Andarine are unknown, as it never completed clinical trials. The FDA warns that SARMs carry serious risks.⁶

Distinctive and Serious Side Effects of Andarine:

• Visual Disturbances (Most Notorious): This is the key reason its clinical development was halted. Users often report altered color perception (a yellowish tint or xanthopsia) and impaired night vision (difficulty adjusting to low light).⁷ These effects are usually dose-dependent and reversible upon cessation, but they represent a clear toxicity signal.

• Testosterone Suppression: While considered less suppressive than S-23, Andarine will suppress the body's natural testosterone production, often requiring the implementation of a Post-Cycle Therapy (PCT).

Other Potential SARMs Side Effects (Warned by FDA):

• Liver Injury: Cases of liver damage and acute liver failure have been reported with SARM use.⁸

• Cardiovascular Risk: Increased risk of heart attack or stroke.⁹

• Cholesterol Changes: Adverse impact on lipid profiles (decreased HDL, increased LDL).

• Sleep Disturbances, Sexual Dysfunction, and Infertility.¹⁰

 Frequently Asked Questions (FAQs)

1. Is Andarine (S-4) a more potent SARM than Ostarine (MK-2866)?

   Andarine (S-4) is often anecdotally considered more potent for immediate strength and visual muscle "hardness" than Ostarine (MK-2866), particularly in cutting cycles. However, Ostarine is generally considered the "milder" SARM, with fewer reported severe side effects and a better track record in clinical trials, making it often preferred for a first-time SARM user.

2. Is there a safe or established dosage for Andarine?

   No. Because Andarine is an investigational, unapproved drug, there is no medically established, prescribed, or safe dosage for human consumption.11 The dosages discussed on online forums (often $25 \text{ mg}$ to $75 \text{ mg}$) are purely anecdotal and carry a high risk of adverse effects, particularly the visual disturbances.

3. What causes the visual side effects associated with S-4?

   The visual disturbances (yellow tint and night blindness) are believed to be caused by an S-4 metabolite interacting with receptors in the retina of the eye, leading to temporary visual changes.

4. Can Andarine cause liver damage?

   Yes. Like most SARMs, the FDA and various health authorities warn that the use of Andarine and other SARMs is associated with a risk of liver injury and acute liver failure.12 This underscores the significant and known danger of using these unapproved compounds.

Crucial Warning: The use of Andarine (S-4) for human consumption is highly risky. It is an unapproved, banned substance with known adverse side effects, including visual impairment and potential liver and heart issues. Consult a healthcare professional for advice on safe and legal ways to achieve your health and fitness goals.