What are the guidelines for starting Depo Provera (medroxyprogesterone acetate)?

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Starting Depo-Provera (Medroxyprogesterone Acetate)

Administer the first Depo-Provera injection ONLY during the first 5 days of a normal menstrual period to ensure the patient is not pregnant, using either 150 mg intramuscularly or 104 mg subcutaneously, with repeat injections scheduled every 13 weeks. 1

Timing of First Injection

Standard Initiation

  • Give the first injection only during the first 5 days of a normal menstrual period 1
  • This timing ensures the patient is not pregnant and provides immediate contraceptive protection 1

Postpartum Initiation

  • For non-breastfeeding women: administer within the first 5 days postpartum 1
  • For exclusively breastfeeding women: delay until the sixth postpartum week 1

Quick-Start/Mid-Cycle Initiation

  • Quick-start initiation is acceptable if you are reasonably certain the patient is not pregnant 2
  • When using quick-start, require backup contraception (condoms or abstinence) for 7 days after the first injection 2

Dosing and Administration

Two Equivalent Formulations

  • Intramuscular (IM): 150 mg by deep intramuscular injection in the gluteal or deltoid muscle 1, 3
  • Subcutaneous (SC): 104 mg subcutaneously 2
  • Both formulations have equivalent effectiveness and side effects 2

Dosing Schedule

  • Schedule repeat injections every 13 weeks (91 days) 4, 2
  • Consider scheduling adolescents every 11-12 weeks to allow buffer time for missed appointments 2
  • The injection can be given up to 2 weeks late (15 weeks from last injection) without requiring additional contraceptive protection 4, 2
  • If more than 15 weeks have elapsed, verify the patient is not pregnant before administering the next injection and use backup contraception for 7 days 2

Essential Pre-Injection Counseling

Menstrual Changes (Most Important)

  • Nearly all patients experience menstrual irregularities initially with unpredictable spotting and bleeding 2
  • Bleeding patterns typically improve over time, with amenorrhea becoming common (57% by end of first year) 3
  • Pre-injection counseling about menstrual changes significantly reduces discontinuation rates 2
  • Reassure patients that amenorrhea is not harmful and does not require intervention 5

Weight Gain

  • Weight gain occurs in some but not all patients 2
  • Early weight gain (>5% at 6 months) is a significant predictor of future excessive weight gain 2

Bone Mineral Density

  • DMPA causes reversible reductions in bone mineral density, but BMD substantially recovers after discontinuation 2
  • Do not limit use to 2 years despite FDA black-box warning, as the benefits of pregnancy prevention outweigh the risks 2
  • Counsel all patients on skeletal health promotion: daily calcium and vitamin D intake, regular weight-bearing exercise, and avoidance of smoking and alcohol 2

Return to Fertility

  • Ovulation suppression may persist for 9-18 months after the last injection 2
  • Time to ovulation after discontinuation varies widely, with the majority ranging from 15 to 49 weeks 2
  • DMPA does not permanently affect fertility 6

Contraceptive Efficacy

  • Failure rate is less than 1% with perfect use (0-0.7% in clinical studies) 1
  • Typical use failure rate is approximately 6% in the first year 2
  • Effectiveness depends on the patient returning every 13 weeks for reinjection 1

STI Protection

  • Counsel patients to use condoms at all times for STI protection, as DMPA provides no protection against sexually transmitted infections 2

Contraindications to Screen For

  • Undiagnosed vaginal bleeding 1
  • Known or suspected breast malignancy 1
  • Current thromboembolic disorders or cerebrovascular disease 1
  • Liver dysfunction 1
  • Known or suspected pregnancy 1

Special Populations

HIV-Infected Patients

  • Inform HIV-infected women that DMPA may or may not increase HIV transmission risk to partners 2
  • Counsel to continue condom use for HIV prevention 2
  • DMPA has no significant interactions with antiretroviral agents 2

Self-Administration Option

  • The subcutaneous 104 mg formulation can be prescribed for self-administration as an off-label use 4
  • Provide instruction (in-person or via telemedicine) on self-injection technique and sharps disposal 4
  • Ensure access to follow-up care for questions or to switch methods 4
  • Provide reinjection reminders 4

Common Pitfalls to Avoid

  • Do not wait for a menstrual period to return before giving subsequent injections, as many users are amenorrheic and waiting increases pregnancy risk 7
  • Do not fail to counsel about menstrual irregularities before the first injection, as this significantly reduces discontinuation 2
  • Do not assume amenorrhea after DMPA is pathologic without ruling out other causes 2
  • Do not routinely monitor bone density or limit use to 2 years based solely on BMD concerns 2
  • Do not forget to verify no contraindications before initiating, particularly pregnancy status 1

Monitoring and Follow-Up

  • No routine follow-up is required 4
  • Encourage patients to contact you at any time to discuss side effects, change methods, or address concerns about reinjection 4
  • Be alert for ectopic pregnancy in patients who become pregnant or complain of severe abdominal pain 1

References

Guideline

DMPA Injection Dosing and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

3-month contraceptive injection approved.

FDA medical bulletin : important information for health professionals from the U.S. Food & Drug Administration, 1993

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

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

The British journal of family planning, 1999

Research

Long-acting injectable contraception with depot medroxyprogesterone acetate.

American journal of obstetrics and gynecology, 1994

Guideline

Switching from Depo-Provera to Seasonale

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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