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Medroxyprogesterone acetate

Medroxyprogesterone acetate injectable suspension is indicated for use by females of reproductive potential to prevent pregnancy. Limitations of Use:.

Prescription medicine Intramuscular Safety alerts on record

How to use Medroxyprogesterone acetate

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Serious warning: LOSS OF BONE MINERAL DENSITY Women who use medroxyprogesterone acetate injectable suspension may lose significant bone mineral density. Bone loss is greater with increasing duration of use and may not be completely reversible [see Warnings and Precautions (5.1)] . …
Who it is for

Medroxyprogesterone acetate injectable suspension is indicated for use by females of reproductive potential to prevent pregnancy. Limitations of Use: The use of medroxyprogesterone acetate injectable suspension is not recommended as a long-term (i.e., longer than 2 years) birth control method unless other options are considered inadequate [see Dosage and Administration (2.1) and Warnings and Precautions (5.1)]. Medroxyprogesterone acetate is a progestin indicated for use by females of reproductive potential to prevent pregnancy. …

How to take it and how often
  • The recommended dose is 150 mg of medroxyprogesterone acetate injectable suspension every 3 months (13 weeks) administered by deep, intramuscular (IM) injection in the gluteal or deltoid muscle
  • Prevention of Pregnancy The 1 mL prefilled syringe of medroxyprogesterone acetate injectable suspension should be vigorously shaken just before use to ensure that the dose being administered represents a uniform suspension
  • The recommended dose is 150 mg of medroxyprogesterone acetate injectable suspension every 3 months (13 weeks) administered by deep intramuscular (IM) injection using strict aseptic technique in the gluteal or deltoid muscle, rotating the sites with every injection
  • As with any IM injection, to avoid an inadvertent subcutaneous injection, body habitus should be assessed prior to each injection to determine if a longer needle is necessary particularly for gluteal IM injection
  • Use for longer than 2 years is not recommended (unless other birth control methods are considered inadequate) due to the impact of long-term medroxyprogesterone acetate injectable suspension treatment on bone mineral density (BMD) [see Warnings and Precautions ]
  • Dosage does not need to be adjusted for body weight [ see Clinical Studies ]
  • To ensure the patient is not pregnant at the time of the first injection, the first injection should be given ONLY during the first 5 days of a normal menstrual period; ONLY within the first 5-days postpartum if not breast-feeding; and if exclusively breast-feeding, ONLY at the sixth postpartum week. …
Strengths it comes in

Prefilled syringe is available packaged with 22-gauge x 1 1/2 inch Terumo SurGuard ® Needles. (3) Prefilled syringe: prefilled syringe is available packaged with 22-gauge x 1 1/2 inch Terumo SurGuard ® Needles. ( 3 )

Children
  • Medroxyprogesterone acetate injectable suspension is not indicated before menarche
  • Use of medroxyprogesterone acetate injectable suspension is associated with significant loss of BMD
  • This loss of BMD is of particular concern during adolescence and early adulthood, a critical period of bone accretion
  • In adolescents, interpretation of BMD results should take into account patient age and skeletal maturity
  • It is unknown if use of medroxyprogesterone acetate injectable suspension by younger women will reduce peak bone mass and increase the risk of osteoporotic fractures in later life. …
Older adults

This product has not been studied in post-menopausal women and is not indicated in this population.

While you are taking it
  • "See FDA-approved patient labeling (Patient Information)." Advise patients at the beginning of treatment that their menstrual cycle may be disrupted and that irregular and unpredictable bleeding or spotting results, and that this usually decreases to the point of amenorrhea as treatment with medroxyprogesterone acetate injectable suspension continues, without other therapy being required
  • Counsel patients about the possible increased risk of breast cancer in women who use medroxyprogesterone acetate injectable suspension [ see Warnings and Precautions ]
  • Counsel patients that this product does not protect against HIV infection (AIDS) and other sexually transmitted diseases. …
Talk to a doctor first if
  • The use of medroxyprogesterone acetate injectable suspension is contraindicated in the following conditions: Known or suspected pregnancy or as a diagnostic test for pregnancy
  • Active thrombophlebitis, or current or past history of thromboembolic disorders, or cerebral vascular disease [ see Warnings and Precautions ]
  • Known or suspected malignancy of breast [ see Warnings and Precautions ]. …
Medicines it may not mix with

Drugs or herbal products that induce certain enzymes, including CYP3A4, may decrease the effectiveness of contraceptive drug products. Counsel patients to use a back-up method or alternative method of contraception when enzyme inducers are used with medroxyprogesterone acetate injectable suspension. ( 7.1 ) 7.1 Changes in Contraceptive Effectiveness Associated With Co-Administration of Other Products If a woman on hormonal contraceptives takes a drug or herbal product that induces enzymes, including CYP3A4, that metabolize contraceptive hormones, counsel her to use additional contraception or a different method of contraception. …

Warnings

Thromboembolic Disorders: Discontinue medroxyprogesterone acetate injectable suspension in patients who develop thrombosis. ( 5.2 ) Cancer Risks: Monitor women with a strong family history of breast cancer carefully. ( 5.3 ) Ectopic Pregnancy: Consider ectopic pregnancy if a woman using medroxyprogesterone acetate injectable suspension becomes pregnant or complains of severe abdominal pain. ( 5.4 ) Anaphylaxis and Anaphylactoid Reactions: Provide emergency medical treatment. ( 5.5 ) Liver Function: Discontinue medroxyprogesterone acetate injectable suspension if jaundice or disturbances of liver function develop. ( 5. 7) Carbohydrate Metabolism: Monitor diabetic patients carefully. …

Possible side effects

The following important adverse reactions observed with the use of medroxyprogesterone acetate injectable suspension are discussed in greater detail in the Warnings and Precautions section ( 5 ): Loss of Bone Mineral Density [ see Warnings and Precautions ( 5.1 ) ] Thromboembolic disease [ see Warnings and Precautions ( 5.2 ) ] Breast Cancer [ see Warnings and Precautions ( 5.3 ) ] Anaphylaxis and Anaphylactoid Reactions [ see Warnings and Precautions ( 5.5 ) ] Bleeding Irregularities [ see Warnings and Precautions ( 5. 10) ] Weight Gain [ see Warnings and Precautions ( 5. …

Pregnancy and breastfeeding

8.1 Pregnancy Medroxyprogesterone acetate injectable suspension should not be administered during pregnancy. [ See Contraindications and Warnings and Precautions ( 5.1 7).]

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2022-12-14.

Brands around the world

Products with Medroxyprogesterone acetate as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

PremproESTROGENS, CONJUGATED .625 mg/1, MEDROXYPROGESTERONE ACETATE 2.5 mg/1 · Tablet, Sugar Coated · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC 0046-1107Label
Medroxyprogesterone AcetateMEDROXYPROGESTERONE ACETATE 10 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.
NDC 0555-0779Label
Medroxyprogesterone AcetateMEDROXYPROGESTERONE ACETATE 150 mg/mL · Injection, Suspension · Eugia US LLC
NDC 55150-329Label
Medroxyprogesterone AcetateMEDROXYPROGESTERONE ACETATE 150 mg/mL · Injection, Suspension · Eugia US LLC
NDC 55150-330Label
PremphaseKit · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC 0046-2575Label

Nigeria (NAFDAC)

NAFDACVerasafe Injection A4-100888NAFDACTriclofem Injection A4-100701NAFDACDepo-Provera 150 mg/mL Injection 04-2310NAFDACMedogen 150 mg/mL Suspension for Injection A4-101057

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01U.S. FDA Class II
25 Apr 2025 · Mckesson Medical-Surgical Inc. Corporate Office · OngoingSevere thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recomme
medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL, Rx only, 1 mL Single-Dose Vial, Mfd in India for: Eugia US LLC, NJ 08520 NDC 55150-329-01 Shipper label: medrU.S. FDA Class II
18 Dec 2024 · Eugia US LLC · OngoingCGMP Deviations
MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402U.S. FDA Class II
7 Oct 2022 · Pharmacy Plus, Inc. dba Vital Care Compounder · OngoingLack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun PhaU.S. FDA Class II
6 May 2022 · SUN PHARMACEUTICAL INDUSTRIES INC · TerminatedLack of assurance of sterility

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Medroxyprogesterone acetate

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

Questions about Medroxyprogesterone acetate

What is Medroxyprogesterone acetate used for?

Medroxyprogesterone acetate injectable suspension is indicated for use by females of reproductive potential to prevent pregnancy. Limitations of Use: The use of medroxyprogesterone acetate injectable suspension is not recommended as a long-term (i.e., longer than 2 years) birth control method unless other options are considered inadequate [see Dosage and Administration (2.1) and Warnings and Precautions (5.1)]. Medro (From the official U.S. FDA label.)

How do I take Medroxyprogesterone acetate?

Follow your prescription or the leaflet in your pack. The official label says: The recommended dose is 150 mg of medroxyprogesterone acetate injectable suspension every 3 months (13 weeks) administered by deep, intramuscular (IM) injection in the gluteal or deltoid muscle. (2.1) 2.1 Prevention of Pregnancy The 1 mL prefilled syringe of medroxyprogesterone acetate injectable suspension should be vigorously shaken just before use to ensure that the dose bei…

Do I need a prescription for Medroxyprogesterone acetate?

Usually yes. Medroxyprogesterone acetate is a prescription medicine in most countries. Rules differ by country.

What brands contain Medroxyprogesterone acetate?

Medroxyprogesterone acetate is sold under names such as Depo-provera, Provera, Depo-subq Provera, Medroxyprogesterone Acetate. Brand names differ between countries.

How can I check that my Medroxyprogesterone acetate is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.