What is the recommended dose for intramuscular (IM) depo medroxyprogesterone acetate (DMPA)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 10, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Recommended Dose for Intramuscular (IM) Depo Medroxyprogesterone Acetate (DMPA)

The recommended dose for intramuscular (IM) depo medroxyprogesterone acetate (DMPA) is 150 mg administered by deep IM injection every 3 months (13 weeks) in the gluteal or deltoid muscle. 1

Administration Guidelines

  • The 1 mL vial or prefilled syringe should be vigorously shaken just before use to ensure uniform suspension 1
  • DMPA can be administered up to 2 weeks late (15 weeks from the last injection) without requiring additional contraceptive protection 2
  • Many healthcare providers schedule visits every 11-12 weeks for adolescents to allow for missed or delayed visits 2
  • The first injection must be given only during the first 5 days of a normal menstrual period, within the first 5 days postpartum if not breastfeeding, or at the sixth postpartum week if exclusively breastfeeding 1

Efficacy and Mechanism

  • DMPA is highly effective with a first-year pregnancy rate of approximately 6% with typical use 2
  • After injection, MPA is detected in serum within 30 minutes and plateaus at about 1.0 ng/mL for about three months 3
  • Ovulation is inhibited as long as MPA levels remain above 0.1 ng/mL, which can persist for up to 9 months after a single injection 3
  • DMPA works through multiple mechanisms including inhibition of ovulation, thickening of cervical mucus, and causing endometrial atrophy 3

Formulation Options

  • Two formulations of DMPA are available:
    • 150 mg delivered intramuscularly (DMPA-IM) 2
    • 104 mg delivered subcutaneously (DMPA-SC) 2
  • Both formulations have similar effectiveness and side effects 2
  • DMPA-SC can be self-administered, which may improve contraceptive access and reproductive autonomy 2

Common Side Effects and Management

  • Menstrual irregularities occur in nearly all patients initially but typically improve over time 2, 4
  • Weight gain may occur, with studies showing that weight gain status at 6 months is a strong predictor of future excessive weight gain 2, 4
  • DMPA causes reductions in bone mineral density (BMD), which prompted an FDA black box warning in 2004 4
  • All patients should be counseled about measures to promote skeletal health, including daily intake of 1300 mg of calcium and 600 IU of vitamin D and regular weight-bearing exercise 2, 4

Long-Term Use Considerations

  • Despite the FDA black box warning about BMD loss, ACOG does not advise limiting DMPA use to 2 years or routinely monitoring bone density after that timeframe 4
  • Substantial recovery of BMD occurs after discontinuation of DMPA 4
  • Return to fertility may be delayed for 9-18 months after discontinuation 5, 6

Special Considerations

  • DMPA can be initiated on the same day as the visit ("quick start") if the provider is reasonably certain the patient is not pregnant 2
  • When starting DMPA, patients should be counseled to use a backup method (e.g., condoms or abstinence) for at least the first week for contraceptive efficacy 2
  • Pre-use counseling about expected menstrual changes is essential to minimize discontinuation rates 7

Common Pitfalls to Avoid

  • Failing to shake the vial/syringe vigorously before administration, which can result in inadequate dosing 1
  • Not counseling patients about expected menstrual changes, which may lead to unnecessary discontinuation 2, 7
  • Overlooking the need for calcium and vitamin D supplementation in long-term users 2, 4
  • Unnecessarily limiting DMPA use to 2 years due to BMD concerns when the benefits of preventing unwanted pregnancy often outweigh these risks 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Pharmacokinetics of depot medroxyprogesterone acetate contraception.

The Journal of reproductive medicine, 1996

Guideline

Risks of Long-Term Depo Provera Use Beyond 2 Years

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Workup for Secondary Amenorrhea Following Depo Provera Use

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Long-acting injectable contraception with depot medroxyprogesterone acetate.

American journal of obstetrics and gynecology, 1994

Research

Depo Provera. Position paper on clinical use, effectiveness and side effects.

The British journal of family planning, 1999

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.