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Drospirenone

孕激素 C

Drospirenone

Drospirenone

Oral

Drospirenone is a synthetic progestogen structurally derived from spironolactone, possessing simultaneous anti-androgenic and anti-mineralocorticoid (spironolactone-like) activity. A non-mainstream option in transfeminine HRT, its unique pharmacological profile may be valuable in select scenarios [1] .

Drospirenone has multiple pharmacological activities:

  • Progestogenic activity: Binds progesterone receptors
  • Anti-androgenic activity: Competitive androgen receptor binding (similar mechanism to spironolactone)
  • Anti-mineralocorticoid activity: Spironolactone-like diuretic effect
  • No estrogenic or glucocorticoid activity

Drospirenone is the only progestogen that combines anti-androgenic and anti-mineralocorticoid activity. For users seeking both progestogenic effects and mild anti-androgenic coverage, drospirenone may reduce the need for a separate anti-androgen.

SourceDoseNotes
In oral contraceptives 3-4 mg/day Combined with ethinylestradiol (NOT recommended for HRT)
Single-agent 4 mg/day Slynd (drospirenone-only pill)
HRT adjunct (exploratory) 3-4 mg/day No large-scale HRT clinical trial data
BrandFormulationNotes
Slynd4 mg drospirenone onlyEE-free, suitable for HRT
Yaz / Yasmin3 mg drospirenone + EEContains ethinylestradiol, PROHIBITED for HRT
GenericsVariousConfirm EE-free
  • K+ (potassium): Drospirenone has spironolactone-like potassium-sparing effects; monitor potassium
  • PRL: Every 6 months
  • If co-administered with spironolactone, hyperkalemia risk increases significantly