Prescription medication · Progestogen
medroxyprogesterone
Also sold as Provera, Depo-Provera. This medicine is used to prevent pregnancy in women who are able to have children.
Data updated 2026-05-15
- 26,589
- FDA reports
- 11
- InteractionsSeveral interactions
- 99% less
- Generic vs brandHuge savings
- 2
- Recall records
What the data shows
medroxyprogesterone (Provera) is a prescription Progestogen, with 26,589 FDA adverse-event reports on file, whose generic costs a fraction of the brand (about 99% less).
Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.
medroxyprogesterone (Provera) is a prescription Progestogen. This medicine is used to prevent pregnancy in women who are able to have children.
Medroxyprogesterone acetate injection is a medicine used to prevent pregnancy in women. It is given as a shot every 3 months.
Verify with FDA → · CMS NADAC pricing →
Drug Pricing (NADAC)
Brand Price
$53.04/unit
Generic Price
$0.13/unit
Generic Savings
99%
Generic Available
Yes (10 manufacturers)
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
This medicine is used to prevent pregnancy in women who are able to have children.
Common side effects
Irregular periods or spotting, No periods, Abdominal pain or discomfort
Key warnings
This medicine can cause you to lose bone mineral density.
The sections below are summarized in plain English from medroxyprogesterone's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
This medicine is a progestin, a synthetic form of the natural hormone progesterone. It prevents pregnancy mainly by stopping the release of an egg from your ovary. It also changes the lining of the uterus, making it harder for a fertilized egg to implant.
How to Take It
You will receive a 150 mg injection of this medicine every 3 months (13 weeks). The shot is given into a muscle, either in your buttock or upper arm. Make sure to shake the syringe well before the injection. To prevent pregnancy, get your first shot within the first 5 days of your period.
This is a plain-language summary of medroxyprogesterone's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
You should not use this medicine if you are pregnant or think you might be pregnant. Small amounts of this medicine can pass into breast milk.
This is a plain-language summary of medroxyprogesterone's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
If you miss a scheduled injection, contact your doctor as soon as possible to reschedule. If you are late for your injection by more than 13 weeks, your doctor should make sure you are not pregnant before giving you the injection.
This is a plain-language summary of medroxyprogesterone's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store at room temperature between 68° to 77°F.
Side Effects (from patient reports)
Based on 26,589 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for medroxyprogesterone, by number of reports
- Breast cancer in women
Breast cancer in women
9,772 reports
- Breast cancer
Breast cancer
8,167 reports
- Brain tumor (meningioma) 1,680
Brain tumor (meningioma)
1,680 reports
- Breast cancer that has spread 1,385
Breast cancer that has spread
1,385 reports
- Feeling sick to your stomach 1,039
Feeling sick to your stomach
1,039 reports
- Headache 987
Headache
987 reports
- Pain 984
Pain
984 reports
- Feeling sad or hopeless 900
Feeling sad or hopeless
900 reports
- Feeling tired 861
Feeling tired
861 reports
- Weight gain 814
Weight gain
814 reports
What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.
Serious Warnings
This medicine can cause you to lose bone mineral density. The longer you use it, the more bone density you may lose. It is not known if this bone loss can be fully reversed. Using this medicine as a teenager or young adult may reduce your peak bone mass and increase your risk of osteoporosis later in life. Because of this risk, it is not recommended for long-term use (longer than 2 years) unless other birth control options are not adequate.
Known Drug Interactions
albuterol, systemic and inhaled mebendazole amoxicillin medroxyprogesterone ampicillin, with or without sulbactam methylprednisolone atenolol metronidazole azithromycin metoprolol caffeine, dietary ingestion nadolol cefaclor nifedipine co-trimoxazole (trimethoprim and sulfamethoxazole) nizatidine diltiazem norfloxacin dirithromycin ofloxacin enflurane omeprazole famotidine prednisone, prednisolone felodipine ranitidine finasteride rifabutin hydrocortisone roxithromycin isoflurane Sorbitol (purgative doses do not inhibit theophylline absorption) isoniazid sucralfate isradipine terbutaline,...
Mechanism: Medroxyprogesterone is a hormone that can change the speed at which your liver clears theophylline from your system.
What to do: Your doctor may need to adjust your theophylline dosage when you start or stop taking this hormone medication.
The following laboratory tests may be affected by progestins including medroxyprogesterone acetate injectable suspension: (a) Plasma and urinary steroid levels are decreased (e.g., progesterone, estradiol, pregnanediol, testosterone, cortisol).
Mechanism: Medroxyprogesterone can lower the amount of estradiol found in your blood and urine.
What to do: Your doctor should keep this in mind when checking your hormone levels or reading lab reports.
John’s wort topiramate HIV protease inhibitors and non-nucleoside reverse transcriptase inhibitors : Significant changes (increase or decrease) in the plasma levels of progestin have been noted in some cases of coadministration of HIV protease inhibitors.
Mechanism: Topiramate can cause the levels of medroxyprogesterone in your blood to change significantly.
What to do: You should use a backup form of birth control to prevent pregnancy while taking these drugs together.
Counsel patients to use a back-up method or alternative method of contraception when enzyme inducers are used with medroxyprogesterone acetate injectable suspension. The following laboratory tests may be affected by progestins including medroxyprogesterone acetate injectable suspension: (a) Plasma and urinary steroid levels are decreased (e.g., progesterone, estradiol, pregnanediol, testosterone, cortisol). (g) The effects of medroxyprogesterone acetate on lipid metabolism are inconsistent.
Mechanism: Medroxyprogesterone can reduce the levels of progesterone measured in your body.
What to do: Your doctor should be aware of this interaction when testing your hormone levels.
The following laboratory tests may be affected by progestins including medroxyprogesterone acetate injectable suspension: (a) Plasma and urinary steroid levels are decreased (e.g., progesterone, estradiol, pregnanediol, testosterone, cortisol).
Mechanism: Medroxyprogesterone can lower the amount of testosterone found in your blood and urine.
What to do: Your doctor may need to monitor your hormone levels or adjust your dosage if you take these together.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
How often do I get the injection?
Where is the injection given?
What should I do if I miss my injection appointment?
Can I use this medicine long-term?
What are the most common side effects?
Can this medicine affect my bones?
Is it safe to use while breastfeeding?
What if I become pregnant while using this medicine?
Can other medicines affect this injection?
What if I have liver problems?
What are the common side effects of medroxyprogesterone?
Does medroxyprogesterone interact with other medications?
What drug class is medroxyprogesterone?
Is there a generic version of medroxyprogesterone?
Is medroxyprogesterone safe during pregnancy?
Has medroxyprogesterone been recalled?
Active Recalls
Lack 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.
Pharmacy Plus, Inc. dba Vital Care Compounder
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Lowlite Investments, Inc. D/B/A Olympia Pharmacy
Related Medications in Progestogen
Other drugs grouped near medroxyprogesterone - same-class peers and common alternatives.
abiraterone
Zytiga
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Compare with medroxyprogesterone →
anastrozole
Arimidex
Anastrozole is a medicine used to treat breast cancer in women after menopause.
Compare with medroxyprogesterone →
bazedoxifene/conjugated estrogens
Duavee
Duavee is a combination medicine containing estrogen and a drug that blocks estrogen in some parts of the body.
Compare with medroxyprogesterone →
cabergoline
Dostinex
Cabergoline is a medicine that helps lower the amount of prolactin in your body.
Compare with medroxyprogesterone →
clomiphene
Clomid, Serophene
Clomiphene citrate is a medicine that helps women ovulate.
Compare with medroxyprogesterone →
Medication Guides
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FDA requirements, cost savings, and when the difference matters
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Common Drug Interactions
Dangerous medication combinations and how to protect yourself
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What the FDA Data Shows for medroxyprogesterone
The FDA label for medroxyprogesterone (sold under brand names such as Provera, Depo-Provera) classifies it as a prescription-only medication in the Progestogen class. This medicine is used to prevent pregnancy in women who are able to have children. Official labeling lists 8 commonly reported side effects, including Irregular periods or spotting, No periods, Abdominal pain or discomfort.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 26,589 voluntary reports. The database also lists 11 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. NADAC pricing from CMS shows a generic unit cost of $0.13 versus $53.04 for the brand - a 99% generic savings.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history (currently 2 recall records on file), and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: December 14, 2022
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages