Drospirenone and Ethinyl Estradiol side effects: what 43,937 FDA adverse event reports show
Drug class
Progestin
Label matched
Drospirenone (Slynd)
Who reports
43,937 reports · 78% serious · 664 with death outcome · 100% female
Used for
SLYND is a progestin indicated for use by females of reproductive potential to prevent pregnancy. SLYND is a progestin indicated for use by females of reproductive potential to prevent pregnancy. ( 1 )
What it is
SLYND (drospirenone) is for use as an oral contraceptive. It is supplied as clear to a slightly opaque PVC-PVDC/Aluminum blister cards, each holding of 24 white tablets each containing 4 mg of drospirenone, a synthetic progestational compound and 4 green inert tablets.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
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). 1,093 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Withdrawal bleeding irregular | 210 | 2,819.8 1,971.8–4,032.5ROR 2,833.3 · calibrated p 8e-22 ✓ | 389.3 EB05 347.1 · IC025 +7.5 3/3 methods agree | Labeled (related wording) related wording | 100% consumer | not reported in cached trials |
| Gallbladder injury | 1,616 | 2,540.0 2,245.9–2,872.5ROR 2,636.9 · calibrated p 2e-22 ✓ | 395.6 EB05 379.6 · IC025 +8.4 3/3 methods agree | Not in label — unassessed | serious n=1,615 | not reported in cached trials |
| Biliary dyskinesia | 1,428 | 2,532.5 2,222.1–2,886.3ROR 2,617.5 · calibrated p 2e-22 ✓ | 395.1 EB05 378.2 · IC025 +8.4 3/3 methods agree | Not in label — unassessed | serious n=1,429 | not reported in cached trials |
| Cholecystitis chronic | 5,533 | 2,233.9 2,098.6–2,378.0ROR 2,555.6 · calibrated p 2e-22 ✓ | 388.6 EB05 380.1 · IC025 +8.5 3/3 methods agree | Not in label — unassessed | serious PRR 285.4 | not reported in cached trials |
| Gallbladder cholesterolosis | 359 | 1,757.5 1,403.3–2,200.9ROR 1,771.9 · calibrated p 6e-20 ✓ | 364.4 EB05 333.8 · IC025 +7.8 3/3 methods agree | Not in label — unassessed | serious n=360 | not reported in cached trials |
| Cholesterosis | 189 | 1,287.3 977.3–1,695.6ROR 1,292.8 · calibrated p 5e-18 ✓ | 333.3 EB05 295.3 · IC025 +7.3 3/3 methods agree | Not in label — unassessed | serious n=189 | not reported in cached trials |
| Post cholecystectomy syndrome | 193 | 1,067.1 826.9–1,377.0ROR 1,071.8 · calibrated p 3e-17 ✓ | 316.7 EB05 280.9 · IC025 +7.2 3/3 methods agree | Not in label — unassessed | serious n=193 · 71% consumer | not reported in cached trials |
| Gallbladder non-functioning | 354 | 777.4 656.2–921.0ROR 783.7 · calibrated p 6e-16 ✓ | 288.9 EB05 264.5 · IC025 +7.5 3/3 methods agree | Not in label — unassessed | serious n=352 | not reported in cached trials |
| Murphy's sign positive | 18 | 445.2 233.7–848.3ROR 445.4 · calibrated p 2e-11 ✓ | 184.6 EB05 123.5 · IC025 +4.2 3/3 methods agree | Lab value / disease marker | serious n=18 | not reported in cached trials |
| Abnormal withdrawal bleeding | 314 | 253.1 220.7–290.2ROR 254.9 · calibrated p 5e-11 ✓ | 163.2 EB05 148.6 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=67 · 96% consumer | not reported in cached trials |
| Fat intolerance | 32 | 242.6 158.3–371.6ROR 242.7 · calibrated p 4e-10 ✓ | 146.5 EB05 108.6 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=31 | not reported in cached trials |
| Pelvic venous thrombosis | 458 | 223.0 199.7–249.2ROR 225.4 · calibrated p 2e-10 ✓ | 150.6 EB05 139.4 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious n=458 | not reported in cached trials |
| Hepatobiliary scan abnormal | 40 | 216.1 148.6–314.2ROR 216.3 · calibrated p 7e-10 ✓ | 138.6 EB05 106.2 · IC025 +5.2 3/3 methods agree | Reporting / coding artifact | serious n=40 | not reported in cached trials |
| Fear of disease | 547 | 209.5 189.5–231.6ROR 212.1 · calibrated p 3e-10 ✓ | 144.5 EB05 134.6 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious n=546 · 70% consumer | not reported in cached trials |
| Thrombophlebitis superficial | 919 | 203.6 188.6–219.9ROR 208.0 · calibrated p 3e-10 ✓ | 142.0 EB05 134.4 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious n=895 | not reported in cached trials |
| Transverse sinus thrombosis | 153 | 193.8 160.6–233.9ROR 194.5 · calibrated p 7e-10 ✓ | 135.2 EB05 118.2 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=153 | not reported in cached trials |
| Intracranial venous sinus thrombosis | 294 | 177.8 155.5–203.3ROR 179.0 · calibrated p 1e-9 ✓ | 128.2 EB05 116.4 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=293 | not reported in cached trials |
| Gallbladder disorder | 4,051 | 139.8 135.1–144.6ROR 153.9 · calibrated p 4e-9 ✓ | 107.9 EB05 105.2 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious PRR 86.8 | not reported in cached trials |
| Withdrawal bleed | 163 | 137.8 115.7–164.0ROR 138.3 · calibrated p 1e-8 ✓ | 105.5 EB05 92.6 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=60 · 88% consumer | not reported in cached trials |
| Gallbladder pain | 146 | 134.0 111.5–161.0ROR 134.5 · calibrated p 1e-8 ✓ | 103.1 EB05 89.8 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=144 | not reported in cached trials |
| Pulmonary infarction | 505 | 128.4 116.4–141.6ROR 129.8 · calibrated p 2e-8 ✓ | 100.7 EB05 93.5 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=506 | not reported in cached trials |
| Embolism arterial | 243 | 121.0 105.1–139.2ROR 121.6 · calibrated p 3e-8 ✓ | 95.7 EB05 86.0 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=243 | not reported in cached trials |
| Medical diet | 39 | 117.5 82.7–166.9ROR 117.6 · calibrated p 8e-8 ✓ | 90.2 EB05 68.8 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=39 | not reported in cached trials |
| Superior sagittal sinus thrombosis | 157 | 115.1 96.7–137.0ROR 115.5 · calibrated p 5e-8 ✓ | 91.7 EB05 80.2 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=157 | not reported in cached trials |
| Cholecystitis acute | 1,095 | 114.7 107.4–122.4ROR 117.6 · calibrated p 3e-8 ✓ | 92.2 EB05 87.7 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=1,093 | not reported in cached trials |
| Pregnancy on oral contraceptive | 501 | 111.9 101.5–123.2ROR 113.1 · calibrated p 5e-8 ✓ | 90.2 EB05 83.8 · IC025 +6.2 3/3 methods agree | Labeled (related wording) related wording | serious n=349 | not reported in cached trials |
| Biliary colic | 535 | 109.3 99.5–120.0ROR 110.6 · calibrated p 6e-8 ✓ | 88.6 EB05 82.4 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=537 | not reported in cached trials |
| Ovarian vein thrombosis | 27 | 104.0 68.6–157.8ROR 104.1 · calibrated p 3e-7 ✓ | 80.6 EB05 58.2 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=27 | not reported in cached trials |
| Axillary vein thrombosis | 63 | 98.4 75.0–129.0ROR 98.5 · calibrated p 2e-7 ✓ | 79.6 EB05 64.4 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=63 · 73% consumer | not reported in cached trials |
| Post thrombotic syndrome | 76 | 96.3 75.2–123.2ROR 96.4 · calibrated p 2e-7 ✓ | 78.5 EB05 64.8 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=76 | not reported in cached trials |
| Iliac vein occlusion | 10 | 92.1 46.8–181.5ROR 92.2 · calibrated p 3e-6 ✓ | 67.7 EB05 39.3 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=10 | not reported in cached trials |
| Cholecystectomy | 1,785 | 89.0 84.7–93.5ROR 92.7 · calibrated p 2e-7 ✓ | 74.9 EB05 72.0 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious PRR 56.8 | not reported in cached trials |
| Contact lens intolerance | 24 | 85.4 55.3–132.0ROR 85.5 · calibrated p 1e-6 ✓ | 68.7 EB05 48.6 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | 78% consumer | not reported in cached trials |
| Injury | 10,712 | 85.3 83.7–86.9ROR 112.5 · calibrated p 5e-8 ✓ | 72.3 EB05 71.2 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious PRR 64.0 | not reported in cached trials |
| Post gastric surgery syndrome | 12 | 72.3 39.4–132.8ROR 72.3 · calibrated p 8e-6 ✓ | 57.4 EB05 35.0 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=12 | not reported in cached trials |
| Paradoxical embolism | 14 | 71.5 40.8–125.5ROR 71.5 · calibrated p 7e-6 ✓ | 57.6 EB05 36.5 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=14 | not reported in cached trials |
| Deep vein thrombosis (leg blood clot) | 8,259 | 69.1 67.6–70.5ROR 84.8 · calibrated p 4e-7 ✓ | 60.3 EB05 59.3 · IC025 +5.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 45.2 | not reported in cached trials |
| Cholecystitis | 1,489 | 68.3 64.8–72.1ROR 70.7 · calibrated p 1e-6 ✓ | 59.8 EB05 57.2 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious PRR 44.4 | not reported in cached trials |
| Cholelithiasis | 4,101 | 68.2 66.1–70.4ROR 75.1 · calibrated p 9e-7 ✓ | 59.7 EB05 58.1 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious PRR 46.1 | not reported in cached trials |
| Fear of death | 248 | 59.5 52.1–67.9ROR 59.8 · calibrated p 5e-6 ✓ | 52.7 EB05 47.4 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=248 | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Drospirenone and Ethinyl Estradiol as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (0 of 40 signal terms matched).
- NCT00302848 — European Active Surveillance Study (EURAS) (N=59510, phase n/a; 15 AE terms posted; arms: Users of Drospirenone (DRSP); Users of Levonorgestrel (LNG); Users of Other Oral Contraceptives (OCs))
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Pain | 12,869 | 10.2 10.0–10.3ROR 14.0 · calibrated p 0.009 ✓ | 10.0 EB05 9.8 · IC025 +3.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 11.4 | not reported in cached trials |
| Injury | 10,712 | 85.3 83.7–86.9ROR 112.5 · calibrated p 5e-8 ✓ | 72.3 EB05 71.2 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious PRR 64.0 | not reported in cached trials |
| Pulmonary embolism (lung blood clot) | 9,171 | 50.7 49.7–51.7ROR 63.8 · calibrated p 3e-6 ✓ | 45.8 EB05 45.1 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious PRR 33.8 | not reported in cached trials |
| Deep vein thrombosis (leg blood clot) | 8,259 | 69.1 67.6–70.5ROR 84.8 · calibrated p 4e-7 ✓ | 60.3 EB05 59.3 · IC025 +5.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 45.2 | not reported in cached trials |
| Anxiety | 6,895 | 11.8 11.5–12.1ROR 13.8 · calibrated p 0.010 ✓ | 11.5 EB05 11.3 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious PRR 12.2 | not reported in cached trials |
| Emotional distress | 6,361 | 26.3 25.7–27.0ROR 30.6 · calibrated p 2e-4 ✓ | 25.0 EB05 24.5 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious PRR 20.6 | not reported in cached trials |
| Cholecystitis chronic | 5,533 | 2,233.9 2,098.6–2,378.0ROR 2,555.6 · calibrated p 2e-22 ✓ | 388.6 EB05 380.1 · IC025 +8.5 3/3 methods agree | Not in label — unassessed | serious PRR 285.4 | not reported in cached trials |
| Cholelithiasis | 4,101 | 68.2 66.1–70.4ROR 75.1 · calibrated p 9e-7 ✓ | 59.7 EB05 58.1 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious PRR 46.1 | not reported in cached trials |
| Gallbladder disorder | 4,051 | 139.8 135.1–144.6ROR 153.9 · calibrated p 4e-9 ✓ | 107.9 EB05 105.2 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious PRR 86.8 | not reported in cached trials |
| General physical health deterioration | 3,267 | 13.9 13.5–14.4ROR 15.0 · calibrated p 0.007 ✓ | 13.6 EB05 13.2 · IC025 +3.7 3/3 methods agree | Reporting / coding artifact | serious PRR 11.6 | not reported in cached trials |
| Nausea | 2,903 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.837 | 1.8 EB05 1.7 · IC025 +0.8 | Labeled adverse reaction exact term | serious PRR 1.9 | not reported in cached trials |
| Abdominal pain | 2,772 | 5.7 5.5–6.0ROR 6.1 · calibrated p 0.146 | 5.7 EB05 5.5 · IC025 +2.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 5.1 | not reported in cached trials |
| Dyspnoea (shortness of breath) | 2,336 | 2.0 1.9–2.1ROR 2.0 · calibrated p 0.960 | 2.0 EB05 1.9 · IC025 +0.9 | Not in label — unassessed | serious PRR 1.9 | not reported in cached trials |
| Anhedonia | 2,241 | 44.1 42.2–46.0ROR 46.4 · calibrated p 2e-5 ✓ | 40.4 EB05 39.0 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious PRR 32.8 | not reported in cached trials |
| Thrombosis | 2,034 | 12.3 11.8–12.9ROR 12.9 · calibrated p 0.013 ✓ | 12.0 EB05 11.6 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious PRR 9.1 | not reported in cached trials |
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.
- Gallbladder injury — n=1,616, PRR 2,540.0
- Biliary dyskinesia — n=1,428, PRR 2,532.5
- Cholecystitis chronic — n=5,533, PRR 2,233.9
- Gallbladder cholesterolosis — n=359, PRR 1,757.5
- Cholesterosis — n=189, PRR 1,287.3
- Post cholecystectomy syndrome — n=193, PRR 1,067.1
- Gallbladder non-functioning — n=354, PRR 777.4
- Abnormal withdrawal bleeding — n=314, PRR 253.1
- Fat intolerance — n=32, PRR 242.6
- Pelvic venous thrombosis — n=458, PRR 223.0
✓ A hand-written Bradford Hill causality assessment exists for this drug: Drospirenone/ethinyl estradiol ↔ Pulmonary embolism (venous thromboembolism).
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 Drospirenone and Ethinyl Estradiol?
In FDA FAERS, the most frequently co-reported reaction terms for Drospirenone and Ethinyl Estradiol are pain, injury, pulmonary embolism, deep vein thrombosis, anxiety, emotional distress. 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 Drospirenone and Ethinyl Estradiol have an FDA boxed warning?
No. The FDA label retrieved for Drospirenone and Ethinyl Estradiol has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Drospirenone and Ethinyl Estradiol 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
- FDA label via openFDA (set ID db32bc55-f295-4d87-9dbb-0a2f45573dcf, effective 20260827; matched on
openfda.generic_name.exact:"DROSPIRENONE") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,133 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
DROSPIRENONE, results-bearing studies sorted by enrollment)
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.