Halotestos (Halotestin) 50 tabs 10mg/tab Blister

Description

Halotestos (Halotestin) 50 tabs 10mg/tab Blister

Product: Halotestin (Fluoxymesterone) – 10mg Tablets, 100 Tablets per Bottle

Halotestin, containing the active pharmaceutical ingredient Fluoxymesterone, is a synthetic, orally active anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of testosterone. Originally developed in the 1950s and approved by the U.S. Food and Drug Administration (FDA) in 1956, this compound is classified as a Schedule III controlled substance under federal regulations.

Fluoxymesterone exhibits a high ratio of androgenic to anabolic activity, making it a potent androgen. It is known for its ability to bind to the androgen receptor, producing nitrogen retention, increasing protein anabolism, and decreasing amino acid catabolism. The drug has an oral bioavailability of approximately 80% and an elimination half-life of roughly 9.2 hours.

Clinical Indications and Mechanism of Action

In clinical settings, Halotestin is indicated for replacement therapy in males with conditions associated with a deficiency or absence of endogenous testosterone, including primary hypogonadism and hypogonadotropic hypogonadism. It is also used to treat delayed puberty in males when definitively diagnosed. In females, the drug is indicated for the palliation of androgen-responsive recurrent mammary cancer in women who are more than one year but less than five years postmenopausal.

The pharmacological action of fluoxymesterone is mediated through the androgen receptor. The compound stimulates protein synthesis, contributing to increases in muscle strength and physical performance. It also promotes erythropoiesis, the production of red blood cells, by enhancing the production of erythropoietic stimulation factor. This effect, combined with improved nitrogen balance, underpins its use in conditions requiring tissue-building and blood-building properties.

Characteristics for Athletic and Performance Application

Due to its specific pharmacological profile, fluoxymesterone is primarily utilised by athletes seeking to enhance power performance, muscle hardness, and aggression without a significant increase in overall body weight. It is frequently employed in sports requiring explosive strength, such as boxing and other combat disciplines. In bodybuilding, its use is less common as it does not promote substantial muscle bulking.

A key feature of fluoxymesterone is its capacity to activate erythropoiesis and enhance the branching of the capillary network in muscles. This improved blood supply significantly increases both strength and endurance. Importantly, fluoxymesterone does not aromatise and does not convert to estradiol, eliminating oestrogen-related side effects such as water retention and gynaecomastia. However, due to its potent androgenic nature, female athletes are strongly advised against using this drug due to the high risk of virilisation.

Dosage and Administration

This product provides 10mg of fluoxymesterone per tablet, with a total of 100 tablets per bottle. Clinical dosing guidelines vary based on the indication:

• For male hypogonadism: 5 to 20 mg administered orally once daily.

• For delayed puberty in males: 2.5 to 20 mg orally once daily for 4 to 6 months.

• For metastatic breast cancer in females: 10 to 40 mg per day orally in divided doses for three months or longer.

For performance enhancement, dosages are often individualised. It is critical to consult with a qualified healthcare professional to determine the appropriate dosage and to monitor for adverse effects.

Important Safety Information and Warnings

Fluoxymesterone is a potent pharmaceutical agent with a significant side-effect profile. Use of this product carries serious risks, including:

• Hepatotoxicity: As a 17α-alkylated compound, fluoxymesterone can be hepatotoxic. Liver function should be monitored regularly.

• Cardiovascular Effects: Androgens can affect lipid profiles and may increase the risk of cardiovascular events.

• Endocrine Effects: Exogenous administration suppresses endogenous testosterone production through feedback inhibition of pituitary luteinising hormone (LH) and follicle-stimulating hormone (FSH). Oligospermia may occur with prolonged use or excessive dosage.

• Virilisation in Women: Due to its strong androgenic activity, women may experience masculinisation, including hirsutism, voice deepening, and menstrual irregularities.

• Paediatric Use: Androgens should be used with extreme caution in children and only by specialists aware of the adverse effects on bone maturation.

This product is contraindicated in males with carcinoma of the breast or prostate. It should not be used during pregnancy.

Halotestin (Fluoxymesterone) 10mg tablets are available for purchase through our trusted partner. To secure your supply of this potent androgenic compound, please visit the following secure website:

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Top 10 Frequently Asked Questions (FAQs)

1. What is Halotestin used for?
   Halotestin (fluoxymesterone) is a synthetic androgen used clinically for testosterone replacement therapy in men with hypogonadism, to treat delayed puberty in boys, and as palliative therapy for advanced breast cancer in postmenopausal women.

2. How does Halotestin work?
   Fluoxymesterone binds to the androgen receptor, stimulating protein synthesis, promoting nitrogen retention, and enhancing red blood cell production.

3. What is the half-life of Halotestin?
   The elimination half-life of fluoxymesterone after oral administration is approximately 9.2 hours.

4. Does Halotestin aromatise or convert to oestrogen?
   No, fluoxymesterone does not aromatise and does not convert to estradiol. This property reduces the risk of oestrogenic side effects such as water retention and gynaecomastia.

5. What are the common side effects of Halotestin?
   Side effects can include polycythemia, liver toxicity, menstrual irregularities, hirsutism, acne, electrolyte imbalances, libido changes, headache, voice deepening, and dyspepsia.

6. Is Halotestin safe for women?
   Due to its potent androgenic activity, fluoxymesterone is not recommended for female athletes. It can cause significant virilisation, including deepening of the voice, facial hair growth, and menstrual irregularities.

7. Can Halotestin cause liver damage?
   Yes. As a 17α-alkylated oral steroid, fluoxymesterone can be hepatotoxic. Liver function should be monitored regularly during use.

8. What is the recommended dosage of Halotestin?
   Clinical dosages vary: for male hypogonadism, 5-20 mg daily; for delayed puberty, 2.5-20 mg daily for 4-6 months; for breast cancer, 10-40 mg daily in divided doses.

9. How does Halotestin affect testosterone production?
   Exogenous administration of fluoxymesterone suppresses endogenous testosterone production through feedback inhibition of pituitary luteinising hormone (LH).

10. What are the contraindications for Halotestin?
    Halotestin is contraindicated in males with carcinoma of the breast or prostate and should not be used during pregnancy.

References and Reputable Sources

• U.S. National Library of Medicine. DailyMed. HALOTESTIN- fluoxymesterone tablet. https://dailymed.nlm.nih.gov

• Medscape. Androxy, Halotestin (fluoxymesterone) dosing, indications, interactions, adverse effects. https://reference.medscape.com

• Drugs.com. Halotestin: Package Insert / Prescribing Information. https://www.drugs.com

• Wikipedia. Fluoxymesterone. https://en.wikipedia.org

• PubMed. National Center for Biotechnology Information. https://pubmed.ncbi.nlm.nih.gov