Template:Parenteral durations of androgens/anabolic steroids
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Medication | Form | Major brand names | Duration |
---|---|---|---|
Testosterone | Aqueous suspension | Andronaq, Sterotate, Virosterone | 2–3 days |
Testosterone propionate | Oil solution | Androteston, Perandren, Testoviron | 3–4 days |
Testosterone phenylpropionate | Oil solution | Testolent | 8 days |
Testosterone isobutyrate | Aqueous suspension | Agovirin Depot, Perandren M | 14 days |
Mixed testosterone estersa | Oil solution | Triolandren | 10–20 days |
Mixed testosterone estersb | Oil solution | Testosid Depot | 14–20 days |
Testosterone enanthate | Oil solution | Delatestryl | 14–20 days |
Testosterone cypionate | Oil solution | Depovirin | 14–20 days |
Mixed testosterone estersc | Oil solution | Sustanon 250 | 28 days |
Testosterone undecanoate | Oil solution | Aveed, Nebido | 100 days |
Testosterone buciclated | Aqueous suspension | 20 Aet-1, CDB-1781e | 90–120 days |
Nandrolone phenylpropionate | Oil solution | Durabolin | 10 days |
Nandrolone decanoate | Oil solution | Deca Durabolin | 21 days |
Methandriol | Aqueous suspension | Notandron, Protandren | 8 days |
Methandriol bisenanthoyl acetate | Oil solution | Notandron Depot | 16 days |
Metenolone acetate | Oil solution | Primobolan | 3 days |
Metenolone enanthate | Oil solution | Primobolan Depot | 14 days |
Note: All are via i.m. injection. Footnotes: a = TP, TV, and TUe. b = TP and TKL. c = TP, TPP, TiCa, and TD. d = Studied but never marketed. e = Developmental code names. Sources: Main: [1][2][3] Additional: [4][5][6][7] |
Template documentation
See also
- Template:Parenteral potencies and durations of steroidal estrogens
- Template:Parenteral potencies and durations of progestogens
- Template:Structural properties of major testosterone esters
- Template:Structural properties of major anabolic steroid esters
References
- ↑ Hans Schuermann; Rudolf Doepfmer (1960). Fertilitätsstörungen beim Manne. Springer-Verlag. pp. 260–. ISBN 978-3-642-94784-1. https://books.google.com/books?id=m1iqBgAAQBAJ&pg=PA260.
- ↑ Joachim Ufer (1960). Hormontherapie in der Frauenheilkunde: Grundlagen und Praxis. Gruyter. p. 153. https://books.google.com/books?id=wcRsAAAAMAAJ.
- ↑ Willibald Pschyrembel (1968). Praktische Gynäkologie: für Studierende und Ärzte. Walter de Gruyter. p. 600. ISBN 978-3-11-150424-7. https://books.google.com/books?id=vVaTnHDFzZ0C&pg=PA600.
- ↑ William Llewellyn (2011). Anabolics. Molecular Nutrition Llc. pp. 385–394. ISBN 978-0-9828280-1-4. https://books.google.com/books?id=afKLA-6wW0oC&pg=PT385.
- ↑ "More than eight years' hands-on experience with the novel long-acting parenteral testosterone undecanoate". Asian J. Androl. 9 (3): 291–7. May 2007. doi:10.1111/j.1745-7262.2007.00275.x. PMID 17486268.
- ↑ "Testosterone buciclate (20 Aet-1) in hypogonadal men: pharmacokinetics and pharmacodynamics of the new long-acting androgen ester". J. Clin. Endocrinol. Metab. 75 (5): 1204–10. November 1992. doi:10.1210/jcem.75.5.1430080. PMID 1430080.
- ↑ Eberhard Nieschlag; Hermann Behre (29 June 2013). Andrology: Male Reproductive Health and Dysfunction. Springer Science & Business Media. pp. 412–. ISBN 978-3-662-04491-9. https://books.google.com/books?id=05fsCAAAQBAJ&pg=PA412. "Under the auspices of WHO a synthesis programme identified testosterone buciclate as a testosterone ester with long-lasting effectiveness. First tested in monkeys and then in hypogonadal patients, it showed a long effective phase of 3–4 months after a single injection."