Evigrade

Medroxyprogesterone acetate depot

Progestogen-only long-acting injectable contraceptive

ATC code: G03AC06

Updated · Methodology

Indications

How to read tiers A–F
  • AStrong evidence – first or second line in international guidelines
  • BRecommended in selected cases
  • CStudy data contradict each other
  • DBenefit not proven, no documented harm
  • FDocumented harm, or risk without benefit

Mechanism of action

Intramuscular 150 mg or subcutaneous 104 mg injection every 3 months. Suppresses ovulation via gonadotropin suppression. Delayed fertility return – median 10 months after last injection. Reduces bone mineral density with long-term use – per black box, no more than 2 years without reassessment.

Safety

Boxed warning

FDA black box: prolonged use beyond 2 years lowers BMD with possibly incomplete recovery. Use cautiously in teens and women at risk for osteoporosis.

Contraindications

  • Hypersensitivity
  • Pregnancy
  • Unexplained uterine bleeding
  • Breast cancer
  • Severe liver disease
  • Active VTE

Serious adverse effects

  • Bone mineral density (BMD) loss
  • Delayed fertility return (median 10 months)
  • Ectopic pregnancy if method fails

Common adverse effects

  • Weight gain 2–5 kg
  • Amenorrhea (50% by year 1)
  • Irregular bleeding in first 3–6 months
  • Headache
  • Decreased libido
  • Depressive episodes

Pregnancy: can you take Medroxyprogesterone acetate depot?

Do not administer in pregnancy.

Breastfeeding: can you take Medroxyprogesterone acetate depot?

Hale L1 · Compatible

WHO MEC 2015 category 1 from day 1 postpartum. Does not reduce milk supply. Medroxyprogesterone RID about 1%, Hale L1.

RID, infant dose via milk
1%
Maternal half-life
1200 h
Maternal peak time
24.0 h
Peak milk concentration
0 mg/L
Milk-to-plasma ratio
0.7

Reference information, not a clinical decision. Discuss feeding pauses or changes with your physician or an IBCLC.

Practical notes

Timing and administration

First injection in first 5 days of cycle, or any day with negative pregnancy test and 7-day backup. Next at 12–13 weeks. If >2 weeks late – 7-day backup.

Monitoring

If used >2 years – BMD assessment via DEXA every 1–2 years. Calcium 1000–1200 mg and vitamin D 800–1000 IU daily. BMD returns to baseline within 2–3 years after discontinuation.

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Frequently asked

What is Medroxyprogesterone acetate depot used for?

Medroxyprogesterone acetate depot is evaluated for the following indications with varying evidence strength: Contraception (evidence tier A), Contraception during breastfeeding (evidence tier A). See the full indication matrix with dosing and citations above on this page.

What are the side effects of Medroxyprogesterone acetate depot?

Common side effects of Medroxyprogesterone acetate depot (≥ 1 in 100): Weight gain 2–5 kg, Amenorrhea (50% by year 1), Irregular bleeding in first 3–6 months, Headache, Decreased libido, Depressive episodes. See the Safety section for uncommon and serious reactions.

Is Medroxyprogesterone acetate depot safe during pregnancy?

Do not administer in pregnancy.

Is Medroxyprogesterone acetate depot compatible with breastfeeding?

WHO MEC 2015 category 1 from day 1 postpartum. Does not reduce milk supply. Medroxyprogesterone RID about 1%, Hale L1.

Who should not take Medroxyprogesterone acetate depot?

Medroxyprogesterone acetate depot is contraindicated in: Hypersensitivity; Pregnancy; Unexplained uterine bleeding; Breast cancer; Severe liver disease. Full list in the Safety section.

Does Medroxyprogesterone acetate depot carry an FDA boxed warning?

FDA black box: prolonged use beyond 2 years lowers BMD with possibly incomplete recovery. Use cautiously in teens and women at risk for osteoporosis.

Other drugs in this group

Mifepristone, Norelgestromin + Ethinylestradiol (transdermal patch), Norethisterone, Progesterone, micronized, Red clover (Trifolium pratense), Cyproterone acetate + Ethinylestradiol, Estradiol + Nomegestrol acetate, Ethinylestradiol + Levonorgestrel