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Medroxyprogesterone side effects: what 49,530 FDA adverse event reports show

Medroxyprogesterone Acetate · 1,181 reaction terms · 106,977 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Who reports

49,530 reports · 88% serious · 988 with death outcome · 99% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Medroxyprogesterone Acetate Tablets USP are indicated for the treatment of secondary amenorrhea and abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology, such as fibroids or uterine cancer. They are also indicated for use in the prevention of endometrial hyperplasia in nonhysterectomized postmenopausal women who are receiving daily oral conjugated estrogens 0.625 mg tablets.

FDA label, Indications and Usage

What it is

DESCRIPTION Medroxyprogesterone Acetate Tablets USP contain medroxyprogesterone acetate, USP which is a derivative of progesterone. It is a white to off-white, odorless crystalline powder, stable in air, melting between 200 and 210°C.

FDA label, Description section

Boxed warning

CARDIOVASCULAR DISORDERS, BREAST CANCER AND PROBABLE DEMENTIA FOR ESTROGEN PLUS PROGESTIN THERAPY Cardiovascular Disorders and Probable Dementia Estrogen plus progestin therapy should not be used for the prevention of cardiovascular disease or dementia. ( See CLINICAL STUDIES and WARNINGS, Cardiovascular Disorders and Probable Dementia .

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled — boxed warning 1Labeled adverse reaction 2Labeled (related wording) 5Likely indication confounding 3Reporting / coding artifact 1Lab value / disease marker 4Not in label — unassessed 24
What the badges mean

Strongest disproportionality signals

Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,141 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Olfactory groove meningioma218,752.0
1,177.3–65,065.3ROR 8,755.8 · calibrated p 3e-11 ✓
292.5 EB05 201.9 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=21no trial data cached
Meningioma11,2751,443.2
1,389.4–1,499.1ROR 1,868.2 · calibrated p 1e-20 ✓
324.0 EB05 319.0 · IC025 +8.3
3/3 methods agree
Not in label — unassessedserious PRR 212.0 · 78% consumerno trial data cached
Pregnancy with injectable contraceptive1581,175.9
867.0–1,594.7ROR 1,179.6 · calibrated p 2e-17 ✓
297.3 EB05 260.4 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=143no trial data cached
Progesterone receptor assay positive6731,078.8
935.2–1,244.4ROR 1,093.6 · calibrated p 1e-17 ✓
298.8 EB05 280.3 · IC025 +7.8
3/3 methods agree
Lab value / disease markerserious n=667 · 72% consumerno trial data cached
Oestrogen receptor assay positive773897.4
792.0–1,016.7ROR 911.6 · calibrated p 9e-17 ✓
283.3 EB05 266.9 · IC025 +7.8
3/3 methods agree
Lab value / disease markerserious n=766no trial data cached
Meningioma benign590856.8
744.3–986.3ROR 867.1 · calibrated p 2e-16 ✓
278.5 EB05 260.2 · IC025 +7.7
3/3 methods agree
Not in label — unassessedserious n=590 · 79% consumerno trial data cached
Intracranial meningioma malignant53613.6
401.8–936.8ROR 614.2 · calibrated p 7e-14 ✓
228.4 EB05 181.3 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=53no trial data cached
Contralateral breast cancer102408.7
311.1–537.1ROR 409.6 · calibrated p 1e-12 ✓
199.2 EB05 168.8 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=102 · 100% consumerno trial data cached
Breast cancer in situ517285.8
255.6–319.5ROR 288.8 · calibrated p 2e-11 ✓
168.9 EB05 157.0 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=513 · 71% consumerno trial data cached
Breast cancer female9,771242.8
237.2–248.5ROR 302.2 · calibrated p 9e-12 ✓
153.7 EB05 151.2 · IC025 +7.2
3/3 methods agree
Not in label — unassessedserious PRR 101.0 · 89% consumerno trial data cached
Malignant breast lump removal49240.3
169.1–341.4ROR 240.5 · calibrated p 3e-10 ✓
144.3 EB05 113.4 · IC025 +5.4
3/3 methods agree
Not in label — unassessedserious n=49no trial data cached
Biopsy breast abnormal29185.9
120.0–288.0ROR 186.0 · calibrated p 4e-9 ✓
119.0 EB05 86.9 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=29no trial data cached
Breast microcalcification26115.3
74.7–178.0ROR 115.3 · calibrated p 1e-7 ✓
85.0 EB05 61.0 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=26no trial data cached
Breast operation10562.7
51.1–77.0ROR 62.8 · calibrated p 4e-6 ✓
54.1 EB05 46.0 · IC025 +5.1
3/3 methods agree
Reporting / coding artifactserious n=105no trial data cached
Breast lump removal2857.5
38.7–85.3ROR 57.5 · calibrated p 1e-5 ✓
49.1 EB05 35.6 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=28no trial data cached
Breast cancer8,16940.2
39.4–41.1ROR 48.0 · calibrated p 2e-5 ✓
36.8 EB05 36.1 · IC025 +5.2
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 24.2 · 93% consumerno trial data cached
Breast reconstruction3036.6
25.2–53.1ROR 36.6 · calibrated p 1e-4 ✓
33.1 EB05 24.3 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=30no trial data cached
Mammogram abnormal4731.7
23.6–42.6ROR 31.7 · calibrated p 3e-4 ✓
29.2 EB05 22.9 · IC025 +4.0
3/3 methods agree
Lab value / disease markerserious n=45no trial data cached
Anovulatory cycle1430.9
17.9–53.1ROR 30.9 · calibrated p 6e-4 ✓
27.8 EB05 17.6 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
Mastectomy11630.1
24.9–36.3ROR 30.2 · calibrated p 3e-4 ✓
28.0 EB05 24.0 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=116no trial data cached
Endometrial hypertrophy2629.1
19.5–43.2ROR 29.1 · calibrated p 5e-4 ✓
26.8 EB05 19.2 · IC025 +3.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=22no trial data cached
Biopsy breast2028.6
18.2–45.1ROR 28.7 · calibrated p 6e-4 ✓
26.3 EB05 17.9 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=20no trial data cached
Unintended pregnancy64827.9
25.8–30.2ROR 28.3 · calibrated p 4e-4 ✓
26.2 EB05 24.6 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious PRR 17.6no trial data cached
Infertility female8926.3
21.2–32.6ROR 26.3 · calibrated p 6e-4 ✓
24.7 EB05 20.7 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=82 · 79% consumerno trial data cached
Ovarian cancer49924.1
22.0–26.3ROR 24.3 · calibrated p 8e-4 ✓
22.8 EB05 21.2 · IC025 +4.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 15.0 · 80% consumerno trial data cached
Clear cell renal cell carcinoma3623.4
16.8–32.8ROR 23.5 · calibrated p 0.001 ✓
22.0 EB05 16.6 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=36 · 100% clinicianno trial data cached
Endometrial disorder2123.1
14.9–35.8ROR 23.1 · calibrated p 0.002 ✓
21.5 EB05 14.8 · IC025 +3.2
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=21no trial data cached
Breast calcifications4022.2
16.1–30.5ROR 22.2 · calibrated p 0.002 ✓
20.9 EB05 16.0 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=39no trial data cached
Fallopian tube disorder1420.8
12.2–35.6ROR 20.8 · calibrated p 0.003 ✓
19.2 EB05 11.8 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=14no trial data cached
Infertility7020.7
16.3–26.3ROR 20.7 · calibrated p 0.002 ✓
19.7 EB05 16.1 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=64no trial data cached
Endometrial hyperplasia3217.3
12.1–24.6ROR 17.3 · calibrated p 0.005 ✓
16.4 EB05 12.0 · IC025 +3.2
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=30no trial data cached
Pregnancy test positive1516.9
10.1–28.3ROR 16.9 · calibrated p 0.007 ✓
15.5 EB05 9.4 · IC025 +2.6
3/3 methods agree
Lab value / disease marker–no trial data cached
Breast cancer recurrent12016.7
13.9–20.1ROR 16.8 · calibrated p 0.005 ✓
16.1 EB05 13.8 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=120 · 100% consumerno trial data cached
Lymphadenectomy3616.1
11.6–22.5ROR 16.1 · calibrated p 0.006 ✓
15.3 EB05 11.5 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=36no trial data cached
Endometrial cancer8116.1
12.9–20.1ROR 16.1 · calibrated p 0.006 ✓
15.5 EB05 12.8 · IC025 +3.5
3/3 methods agree
Labeled adverse reaction
exact term
serious n=80no trial data cached

Trial evidence (ClinicalTrials.gov)

Trial cross-check not yet run for this drug (ClinicalTrials.gov pull covers the 800 most-reported drugs first).

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Meningioma11,2751,443.2
1,389.4–1,499.1ROR 1,868.2 · calibrated p 1e-20 ✓
324.0 EB05 319.0 · IC025 +8.3
3/3 methods agree
Not in label — unassessedserious PRR 212.0 · 78% consumerno trial data cached
Breast cancer female9,771242.8
237.2–248.5ROR 302.2 · calibrated p 9e-12 ✓
153.7 EB05 151.2 · IC025 +7.2
3/3 methods agree
Not in label — unassessedserious PRR 101.0 · 89% consumerno trial data cached
Breast cancer8,16940.2
39.4–41.1ROR 48.0 · calibrated p 2e-5 ✓
36.8 EB05 36.1 · IC025 +5.2
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 24.2 · 93% consumerno trial data cached
Drug ineffective (drug did not work)1,1180.4
0.3–0.4ROR 0.3 · calibrated p 0.013 ✓
0.4 EB05 0.3 · IC025 -1.6
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.5no trial data cached
Nausea1,0590.6
0.5–0.6ROR 0.6 · calibrated p 0.068
0.6 EB05 0.5 · IC025 -0.9
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.5no trial data cached
Headache1,0080.7
0.6–0.7ROR 0.7 · calibrated p 0.118
0.7 EB05 0.6 · IC025 -0.7
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.7no trial data cached
Pain1,0020.7
0.6–0.7ROR 0.7 · calibrated p 0.122
0.7 EB05 0.7 · IC025 -0.6
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.6no trial data cached
Depression9081.7
1.6–1.8ROR 1.7 · calibrated p 0.768
1.7 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.3no trial data cached
Fatigue (tiredness)8760.5
0.4–0.5ROR 0.5 · calibrated p 0.039 ✓
0.5 EB05 0.5 · IC025 -1.2
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.4no trial data cached
Anxiety7881.2
1.1–1.3ROR 1.2 · calibrated p 0.422
1.2 EB05 1.1 · IC025 +0.1Not in label — unassessedserious PRR 1.0no trial data cached
Oestrogen receptor assay positive773897.4
792.0–1,016.7ROR 911.6 · calibrated p 9e-17 ✓
283.3 EB05 266.9 · IC025 +7.8
3/3 methods agree
Lab value / disease markerserious n=766no trial data cached
Dizziness7460.6
0.6–0.7ROR 0.6 · calibrated p 0.097
0.6 EB05 0.6 · IC025 -0.8
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.6no trial data cached
Off label use (used outside approved label)7120.3
0.3–0.4ROR 0.3 · calibrated p 0.012 ✓
0.3 EB05 0.3 · IC025 -1.6
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.3no trial data cached

Unlabeled candidate signals

These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Medroxyprogesterone acetate ↔ Meningioma.

Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.

Common questions

What are the most reported side effects of Medroxyprogesterone?

In FDA FAERS, the most frequently co-reported reaction terms for Medroxyprogesterone are meningioma, breast cancer female, breast cancer, breast cancer metastatic, nausea, headache. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.

Does Medroxyprogesterone have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: CARDIOVASCULAR DISORDERS, BREAST CANCER AND PROBABLE DEMENTIA FOR ESTROGEN PLUS PROGESTIN THERAPY Cardiovascular Disorders and Probable Dementia Estrogen plus progestin therapy should not be used for the prevention of cardiovascular disease or dementia. ( See CLINICAL STUDIES and WARNINGS, Cardiovascular Disorders and Probable Dementia .

Do FAERS signals prove that Medroxyprogesterone causes these side effects?

No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.

Sources & methods

Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.