Oxymetholone

Medical uses

The primary clinical applications of oxymetholone include treatment of anemia and osteoporosis, as well as stimulating muscle growth in malnourished or underdeveloped patients. However, in the United States, the only remaining -approved indication is the treatment of anemia.

Following the introduction of oxymetholone, nonsteroidal drugs such as epoetin alfa were developed and shown to be more effective as a treatment for anemia and osteoporosis without the side effects of oxymetholone. The drug remained available despite this and eventually found a new use in treating HIV/AIDS wasting syndrome.

Presented most commonly as a 50 mg tablet, oxymetholone has been said to be one of the "strongest" and "most powerful" AAS available for medical use. Similarly, there is a risk of side effects. Oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis. For this reason, it is often used by bodybuilders and athletes.

Non-medical uses

Oxymetholone is used for physique- and performance-enhancing purposes by competitive athletes, bodybuilders, and powerlifters.

Side effects

The common side effects of oxymetholone include depression, lethargy, headache, swelling, fast and excessive weight gain, priapism, changes in skin color, urination problems, nausea, vomiting, stomach pain (if taken on an empty stomach), loss of appetite, jaundice, breast swelling in men, feeling restless or excited, insomnia, and diarrhea. In women, side effects also include acne, changes in menstrual periods, voice deepening, hair growth on the chin or chest, pattern hair loss, enlarged clitoris, and changes in libido. Because of its 17α-alkylated structure, oxymetholone is hepatotoxic. Long term use of the drug can cause a variety of serious ailments, including hepatitis, liver cancer, and cirrhosis; therefore periodic liver function tests are recommended for those taking oxymetholone.

Pharmacology

Pharmacodynamics

Like other AAS, oxymetholone is an agonist of the androgen receptor (AR). It is not a substrate for 5α-reductase (as it is already 5α-reduced) and is a poor substrate for 3α-hydroxysteroid dehydrogenase (3α-HSD), and therefore shows a high ratio of anabolic to androgenic activity.

As a DHT derivative, oxymetholone is not a substrate for aromatase and hence cannot be aromatized into estrogenic metabolites. However, uniquely among DHT derivatives, oxymetholone is nonetheless associated with relatively high estrogenicity, and is known to have the potential to produce estrogenic side effects such as gynecomastia (rarely) and water retention. It has been suggested that this may be due to direct binding to and activation of the estrogen receptor by oxymetholone. Oxymetholone does not possess any significant progestogenic activity.

Pharmacokinetics

There is limited information available on the pharmacokinetics of oxymetholone. It appears to be well-absorbed with oral administration. Oxymetholone has very low affinity for human serum sex hormone-binding globulin (SHBG), less than 5% of that of testosterone and less than 1% of that of DHT. The drug is metabolized in the liver by oxidation at the C2 position, reduction at the C3 position, hydroxylation at the C17 position, and conjugation. The C2 hydroxymethylene group of oxymetholone can be cleaved to form mestanolone (17α-methyl-DHT), which may contribute to the effects of oxymetholone. The elimination half-life of oxymetholone is unknown. Oxymetholone and its metabolites are eliminated in the urine.

Chemistry

Oxymetholone, also known as 2-hydroxymethylene-17α-methyl-4,5α-dihydrotestosterone (2-hydroxymethylene-17α-methyl-DHT) or as 2-hydroxymethylene-17α-methyl-5α-androstan-17β-ol-3-one, is a synthetic androstane steroid and a 17α-alkylated derivative of DHT.

History

Oxymetholone was first described in a 1959 paper by scientists from Syntex. It was introduced for medical use by Syntex and Imperial Chemical Industries in the United Kingdom under the brand name Anapolon by 1961. Oxymetholone was also introduced under the brand names Adroyd (Parke-Davis) by 1961 and Anadrol (Syntex) by 1962. The drug was marketed in the United States in the early 1960s.

Society and culture

Generic names

Oxymetholone is the generic name of the drug and its , , , , and , while oxymétholone is its .

Brand names

Oxymetholone has been marketed under a variety of brand names including Anadrol, Anadroyd, Anapolon, Anasterona, Anasteronal, Anasterone, Androlic, Androyd, Hemogenin, Nastenon, Oxitoland, Oxitosona, Oxyanabolic, Oxybolone, Protanabol, Roboral, Synasterobe, Synasteron, and Zenalosyn.

Availability

United States

Oxymetholone is one of the few AAS that remains available for medical use in the United States. The others (as of August 2023) are testosterone, testosterone cypionate, testosterone enanthate, testosterone undecanoate, methyltestosterone, fluoxymesterone, and nandrolone

Other countries

The availability of oxymetholone is fairly limited and seems to be scattered into isolated markets in Europe, Asia, and North and South America. It is known to be available in Turkey, Greece, Moldova, Iran, Thailand, Brazil, and Paraguay. At least historically, it has also been available in Canada, the United Kingdom, Belgium, the Netherlands, Spain, Poland, The UAE, Israel, Hong Kong, and India.

Legal status

Oxymetholone, along with other AAS, is a schedule III controlled substance in the United States under the Controlled Substances Act.

References

References

1. Anvisa. (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial". [[Diário Oficial da União]].
2. (2022-11-04). "Anabolic steroid misuse".
3. William Llewellyn. (2011). "Anabolics". Molecular Nutrition Llc.
4. (June 2001). "Review of oxymetholone: a 17alpha-alkylated anabolic-androgenic steroid". Clinical Therapeutics.
5. "Oxymetholone Powder Uses".
6. (June 2008). "Pharmacology of anabolic steroids". British Journal of Pharmacology.
7. "Oxymetholone". Springer Nature Switzerland AG.
8. (December 2006). "Anadrol-50". Meda Pharmaceuticals.
9. "Oxymetholone Side Effects". drugs.com.
10. "Anadrol Official FDA Information, Side Effects and Uses". drugs.com.
11. (March 2003). "Double-blind, randomized, placebo-controlled phase III trial of oxymetholone for the treatment of HIV wasting". AIDS.
12. (January 1982). "Spontaneous and Oxymetholone-Induced Gynecomastia.". C/O Allen Press, Inc Po Box 368, Lawrence, Ks 66044: Amer Soc Andrology, Inc..
13. (January 1982). "5-Alpha Reductase Blockade May Be Responsible for Spontaneous and Oxymetholone-Induced Gynecomastia.". Social Apdo Postal 73-032, Mexico Df 03020, Mexico: Inst Mexicano Seguro..
14. (June 1984). "Relative binding affinity of anabolic-androgenic steroids: comparison of the binding to the androgen receptors in skeletal muscle and in prostate, as well as to sex hormone-binding globulin". Endocrinology.
15. (1 April 2015). "Mosby's Drug Reference for Health Professions". Elsevier Health Sciences.
16. (14 November 2014). "The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies". Springer.
17. (January 2000). "Index Nominum 2000: International Drug Directory". Taylor & Francis.
18. (January 1959). "Steroids. CVI. Synthesis of 7β-Methyl Hormone Analogs". Journal of the American Chemical Society.
19. (1961). "Advertisements". Proceedings of the Royal Society of Medicine.
20. (1961). "Advertisements". British Medical Journal.
21. (1961). "Latest Pharmaceutical Preparations". The Central African Journal of Medicine.
22. (August 1962). "New drugs in rheumatic disease". Arthritis and Rheumatism.
23. Matusow, Paul D. (1962). "If - Then; C.A.M.S.I.; In the future". Dalhousie Medical Journal.
24. (6 December 2012). "Concise Dictionary of Pharmacological Agents: Properties and Synonyms". Springer Science & Business Media.
25. "Oxymetholone".
26. Kochakian, Charles D.. (6 December 2012). "Anabolic-Androgenic Steroids". Springer Science & Business Media.
27. "Drugs@FDA: FDA Approved Drug Products". United States Food and Drug Administration.
28. (21 December 2006). "Drug Abuse Handbook, Second Edition". CRC Press.