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degarelix (Firmagon)

FDA approved December 2008 Indications: - treatment of advanced prostate cancer Adverse effects: - minimal to no initial surge in testosterone production - injection site reactions (pain, redness, & swelling) - hot flashes, increased weight, fatigue - increases in serum ALT, serum AST - prolongation of the QT interval [2] Mechanism of action: 1) binds reversibly to GnRH receptors in the pituitary gland & inhibits their interaction with GnRH 2) induces a rapid reduction in plasma LH & plasma FSH, & in turn, plasma testosterone 3) slows growth & progression of prostate cancer by suppressing testosterone secretion by Leydig cells of the testes Notes: - manufactured for Ferring Pharmaceuticals Inc., Parsippany, N.J., by Rentschler Biotechnologie Gmbh, Laupheim, Germany

General

receptor antagonist antineoplastic endocrine agent

Database Correlations

PUBCHEM cid=16186010

References

  1. FDA News release http://www.fda.gov/bbs/topics/NEWS/2008/NEW01935.html
  2. Geriatrics at your Fingertips, 13th edition, 2011 Reuben DB et al (eds) American Geriatric Society
  3. MedlinePlus: Degarelix Injection http://www.nlm.nih.gov/medlineplus/druginfo/meds/a609022.html