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Medroxyprogesterone depot

DEPO-PROVERA

What it isDepot progesterone-receptor agonist that suppresses ovulation; injectable contraception.

Why this oneIt provides private, adherence-forgiving contraception and often suppresses menstruation.

What limits itIrregular bleeding and weight gain are common; delayed fertility return and bone-density loss can end treatment.

FDA label

BOXED WARNING Loss of bone mineral density. Women who use Depo-Provera CI may lose significant BMD; loss is greater with increasing duration of use and may not be completely reversible. Not recommended as long-term (>2 years) birth control unless other options are inadequate.
FDA dosingPopulationStartTargetMax
Prevention of pregnancyFemales of reproductive potential150 mg by deep IM injection (gluteal or deltoid)150 mg IM every 3 months (13 weeks)Use for longer than 2 years not recommended unless other options inadequate

Renal Undefined (effect of renal impairment unknown)

Hepatic Undefined (effect of hepatic impairment unknown; significant liver disease is a contraindication)

150 mg every 3 months (13 weeks); not recommended for use longer than 2 years unless other options inadequate

Instructions

Contraindications

Cautions

Adverse reactions

Pregnancy No use for contraception in pregnancy; discontinue during pregnancy. Epidemiologic studies have not found an increased risk of birth defects with progestins.

Lactation Medroxyprogesterone acetate is detectable in milk; milk composition/quality/amount not adversely affected; in exclusive breastfeeders initiate during or after sixth postpartum week; no adverse effects noted in exposed infants.

NO BOXED WARNINGS

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Medroxyprogesterone depot ballicule

Medroxyprogesterone depot ballicule: receptor binding, kinetics and half-life diagram

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