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 dosing
Population
Start
Target
Max
Prevention of pregnancy
Females of reproductive potential
150 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
Shake vigorously just before use
Give by deep IM injection using strict aseptic technique in gluteal or deltoid muscle, rotating sites
First injection only during first 5 days of a normal menstrual period or within first 5 days postpartum
In mothers who exclusively breastfeed, administer during or after the sixth postpartum week
Dosage does not need adjustment for body weight; if interval >13 weeks, confirm not pregnant before dosing
Contraindications
Active thrombophlebitis, or current or past history of thromboembolic disorders, or cerebral vascular disease
Known or suspected malignancy of breast
Significant liver disease
Undiagnosed vaginal bleeding
Cautions
Loss of bone mineral density
Thromboembolic disorders
Cancer risks (breast, cervical)
Meningioma - discontinue if diagnosed
Ectopic pregnancy
Anaphylaxis and anaphylactoid reactions
Liver function disturbances - discontinue if jaundice/abnormal LFTs
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.