Medroxyprogesterone (Depo-Provera) Dosage and Administration
For contraception, the recommended dosage of Depo-Provera is 150 mg administered by deep intramuscular injection every 3 months (13 weeks) in the gluteal or deltoid muscle. 1
Intramuscular (IM) Administration Guidelines
- The 1 mL vial should be vigorously shaken just before use to ensure uniform suspension 1
- Administer using strict aseptic technique, rotating injection sites with each administration 1
- Body habitus should be assessed prior to each injection to determine if a longer needle is necessary, particularly for gluteal IM injection 1
- First injection timing:
Important Timing Considerations
- If the time interval between injections exceeds 13 weeks, pregnancy should be ruled out before administering the next dose 1
- Efficacy depends on adherence to the dosage schedule 1
- When switching from other contraceptive methods, Depo-Provera should be given in a manner that ensures continuous contraceptive coverage 1
Duration of Use Considerations
- Not recommended as a long-term birth control method (i.e., longer than 2 years) unless other options are considered inadequate due to bone mineral density concerns 1
- Women using Depo-Provera may lose significant bone mineral density, with greater loss occurring with increasing duration of use 1
- Bone loss may not be completely reversible 1
Self-Administration Option
- Self-administered subcutaneous DMPA-SC is now recommended as an additional approach to deliver injectable contraception 2
- Self-administration has been shown to improve contraceptive continuation rates while maintaining equivalent safety and efficacy to provider administration 2
- Provider-administered DMPA should remain available as an option 2
Special Populations and Alternative Uses
For Hormone Replacement Therapy in Premature Ovarian Insufficiency
- When used as part of hormone replacement therapy (HRT) with estrogen:
For Endometriosis Treatment
- Higher doses have been used for endometriosis treatment:
Contraindications
- Active thrombophlebitis or current/history of thromboembolic disorders or cerebral vascular disease 1
- Known or suspected breast malignancy 1
- Known hypersensitivity to medroxyprogesterone acetate or any ingredients 1
- Significant liver disease 1
- Undiagnosed vaginal bleeding 1
Monitoring and Follow-up
- Monitor for bone mineral density changes, especially in adolescents and young adults 1
- Evaluate treatment effect if used for other conditions (e.g., endometriosis) after 3-6 months 2
- For diabetic patients, monitor carbohydrate metabolism carefully 1
Patient Counseling Points
- Inform patients about potential menstrual irregularities (bleeding or spotting), which occur in 57% of users at 12 months and 32% at 24 months 1
- Advise about possible weight gain (38% gain >10 lbs at 24 months) 1
- Discuss other common side effects: abdominal pain/discomfort (11%), dizziness (6%), headache (17%), nervousness (11%), and decreased libido (6%) 1
- Return to fertility may be delayed for several months after discontinuation 6