How should I write the prescription for Depo‑Provera (medroxyprogesterone acetate) 150 mg, including the sig and quantity?

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Last updated: November 6, 2026 • View editorial policy

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How to Write a Prescription for Depo-Provera 150 mg

Write the prescription as: Depo-Provera (medroxyprogesterone acetate) 150 mg/mL intramuscular injection; Sig: Inject 1 mL (150 mg) deep intramuscularly every 12 weeks (84 days); Quantity: 1 mL vial or 1 prefilled syringe.

Prescription Components

Drug Name and Formulation

  • Generic/Brand: Medroxyprogesterone acetate injectable suspension / Depo-Provera CI
  • Strength: 150 mg/mL
  • Route: Intramuscular (IM) only 1

Sig (Directions)

  • Dose: 1 mL (150 mg) deep intramuscular injection
  • Frequency: Every 12 weeks (13 weeks/84 days) 2, 3
  • Timing window: Can be given up to 2 weeks late (15 weeks from last injection) without requiring backup contraception 2

Quantity

  • Dispense: 1 mL single-dose vial OR 1 mL prefilled syringe 1
  • Refills: Write for 3 refills if providing for one year of coverage (4 injections total)

Critical Prescribing Details

Available Formulations

Depo-Provera CI comes in two presentations 1:

  • 1 mL single-dose vial (NDC 0009-0746-30)
  • 1 mL prefilled syringe with 22-gauge × 1.5-inch needle (NDC 0009-7376-11)

Administration Instructions

  • Must shake vigorously before use 1
  • Administer by deep intramuscular injection only
  • Storage: Vials must be stored upright at 20-25°C (68-77°F) 1

Timing of Initiation

When starting Depo-Provera, timing determines need for backup contraception 3:

  • If started within 7 days of menses: No backup needed
  • If started >7 days after menses: Patient must abstain or use barrier methods (condoms) for 7 days
  • Can be started anytime if reasonably certain patient is not pregnant 3

Required Pre-Administration

  • Blood pressure measurement: NOT required (unlike combined hormonal contraceptives) 3
  • Bimanual/pelvic exam: NOT required 3
  • Pregnancy test: Only if uncertain about pregnancy status

Important Counseling Points to Document

Black Box Warning

The FDA label includes a boxed warning about bone mineral density loss 1:

  • Should not be used for more than 2 years unless other methods are inadequate
  • Greatest BMD loss occurs in first 2 years of use
  • Particularly concerning for adolescents during peak bone accretion

Expected Side Effects

Document that patient was counseled about 1:

  • Menstrual changes: 55% amenorrhea at 1 year, 68% at 2 years
  • Irregular bleeding/spotting initially is normal
  • Weight gain: Common side effect
  • Delayed return to fertility: May take up to 18 months after last injection to conceive 1

Special Populations

  • Breastfeeding: Delay initiation until 6 weeks postpartum if exclusively breastfeeding 1
  • Adolescents: Use with caution due to BMD concerns; counsel about bone health 1

Common Pitfalls to Avoid

  1. Don't prescribe the subcutaneous formulation (104 mg/0.65 mL) unless specifically intending off-label self-administration 2
  2. Don't write "every 3 months" - be specific: "every 12 weeks" or "every 84 days"
  3. Don't forget to specify IM route - this distinguishes it from subcutaneous DMPA
  4. Don't prescribe without discussing the 2-year limitation due to BMD concerns
  5. Don't require pelvic exam before prescribing - this is an unnecessary barrier to access 3

Sample Prescription Format

Rx: Depo-Provera (medroxyprogesterone acetate) 150 mg/mL injection
Sig: Inject 1 mL deep intramuscularly every 12 weeks
Disp: 1 mL vial (or 1 mL prefilled syringe)
Refills: 3

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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.