What is Provera (medroxyprogesterone acetate) used for?

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What is Provera Used For?

Provera (medroxyprogesterone acetate) is primarily used for contraception (as injectable Depo-Provera), hormone replacement therapy in combination with estrogen, treatment of abnormal uterine bleeding, and as palliative therapy for advanced endometrial or renal carcinoma. 1, 2

Primary Clinical Indications

Contraception (Injectable DMPA/Depo-Provera)

  • Injectable depot medroxyprogesterone acetate (DMPA) is a highly effective progestin-only contraceptive administered intramuscularly or subcutaneously every 3 months (13 weeks). 1, 3
  • The typical use failure rate is 6%, with perfect use failure rate of 0.2%. 4
  • DMPA works through multiple mechanisms: inhibiting ovulation by suppressing the LH surge, thickening cervical mucus, and inducing endometrial atrophy. 5
  • Both provider-administered and self-administered subcutaneous formulations are acceptable options, with self-administration showing higher continuation rates. 1
  • No time limit exists for DMPA use—the American College of Obstetricians and Gynecologists explicitly states that use should not be limited to 2 years despite FDA black box warnings about bone mineral density. 3, 4

Hormone Replacement Therapy

  • Oral medroxyprogesterone acetate is used in combination with estrogen to provide endometrial protection in postmenopausal women with an intact uterus. 4, 6
  • Doses of 2.5 mg, 5 mg, or 10 mg daily are used in continuous combined regimens, with 5 mg and 10 mg showing better endometrial protection and higher rates of amenorrhea. 6
  • However, natural micronized progesterone is increasingly preferred over synthetic progestins like Provera due to superior cardiovascular and metabolic safety profiles. 4

Abnormal Uterine Bleeding

  • Medroxyprogesterone acetate induces endometrial atrophy and can control heavy bleeding associated with anovulation. 7
  • The progestin causes the endometrium to become atrophic with small, straight endometrial glands and decidualized stroma. 5

Cancer Treatment (Palliative)

  • For advanced endometrial or renal carcinoma, initial doses of 400-1000 mg per week intramuscularly are recommended, with maintenance doses as low as 400 mg per month if disease stabilizes. 2
  • Medroxyprogesterone acetate is used as adjunctive and palliative treatment in advanced inoperable cases, not as primary therapy. 2

Fertility Preservation in Endometrial Cancer

  • Continuous progestin therapy (including medroxyprogesterone) may be used in highly selected patients with stage IA, grade 1 endometrioid adenocarcinoma who desire fertility preservation. 3
  • This approach requires close monitoring with endometrial sampling every 3-6 months and achieves durable complete response in approximately 50% of patients. 3
  • Hysterectomy is recommended if cancer persists after 6 months of progestin therapy. 3

Important Clinical Considerations

Contraindications and Precautions

  • Monthly injectables containing medroxyprogesterone acetate are inappropriate for patients with heart failure due to fluid retention risk. 1
  • For patients with pre-existing osteoporosis risk factors, alternative contraceptive methods may be preferable. 3
  • Verify no contraindications to progestin therapy exist before initiating treatment. 8

Duration of Use and Monitoring

  • For contraceptive use, counsel patients continuing DMPA beyond 2 years about skeletal health measures: 1,300 mg daily calcium, 600 IU daily vitamin D, regular weight-bearing exercise, and smoking cessation. 3
  • Routine bone density monitoring is not recommended after 2 years of DMPA use unless other osteoporosis risk factors are present. 3
  • No routine blood work is required during ongoing DMPA use. 3

Return to Fertility

  • Return to fertility may be delayed 9-18 months after discontinuing injectable DMPA. 3, 8
  • MPA can be detected in serum for as long as 9 months after a single 150 mg injection, and ovulation resumes when MPA levels fall below 0.1 ng/mL. 5

Common Pitfalls to Avoid

  • Do not discontinue DMPA at 2 years based solely on duration concerns, as this increases risk of unintended pregnancy without clear benefit. 3, 4
  • Do not routinely order bone density scans after 2 years of DMPA use unless other osteoporosis risk factors are present. 3
  • Weight gain at 6 months (>5% increase) is a strong predictor of future excessive weight gain with ongoing DMPA use and warrants counseling. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Duration of Provera (Medroxyprogesterone Acetate) Use

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Provera and Progesterone Differences in Clinical Applications

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Pharmacokinetics of depot medroxyprogesterone acetate contraception.

The Journal of reproductive medicine, 1996

Research

The effect of medroxyprogesterone acetate (Provera) on ovarian radiosensitivity.

American journal of obstetrics and gynecology, 1989

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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