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Spironolactone

Indications                                                                                                                                                                                                     

  • no FDA approved derm indications

  • off-label: hirsutism, acne, androgenic alopecia, HS

Pharmacology                                                                                                                                                                                                

  • relatively weak antagonist of the androgen receptor and also provides some inhibition of androgen biosynthesis

  • steroid molecule that resembles mineralocorticoids

  • metabolized to canrenone which is the primary active antiandrogen (and diuretic)

Side Effects                                                                                                                                                                                                    

Menstrual Dysfunction

  • Heavy menstrual bleeding can occur, typically at doses of >100mg

    • reduce dose to 50-75mg​

    • add OCP

    • cycle 3 weeks on 1 week off

    • often improves on own in 2-3 months

Hypotension 

  • It seems there is a dose response relationship between spironolactone and hypotension for doses <50mg daily but not above 50mg daily.  A paper looking at 2084 female patients treated for acne, alopecia, or hirsutism found an ~3% hypotension rate.  Dose did not correlate with development of hypotension. It does not appear that spironolactone causes hypotension in patients being treated for these conditions. 38483433

Hyperkalemia

  • Very uncommon in young and healthy patients (cit needed).  

  • typically affects those with severe renal insufficiency or on other potassium sparing diuretics, or Addison disease

  • if opting to monitor, should be done within 1-4 weeks to minimize the effects of prolonged hyperkalemia. (39033981)

Malignancy

  • Concerns regarding malignancy come from chronic toxicity studies in rats where they were given 25-250 times the dose by weight.  This caused benign adenomas of thyroid and testes, malignant mammary tumors, and proliferative changes in the liver. 

  • A study of 3692 women showed no increased risk of benign or malignant tumors of the breast or uterus with spironolactone use for dermatologic conditions. 38423468 

External Medicine

 Conceived 2016

DISCLAIMER: This website is a collection of primary literature and the opinions of the website creators on that literature.  It is not intended to be used for the practice of medicine or the delivery of medical care in the absence of other appropriate credentials (like a medical degree).  Discuss any information with your doctor before pursuing treatments mentioned on this site.  

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