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Drospirenone and Ethinyl Estradiol side effects: what 43,937 FDA adverse event reports show

Drospirenone And Ethinyl Estradiol · 1,133 reaction terms · 178,006 drug–reaction co-reports · data 2026-09-14
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Drug class

Progestin

FDA label, Indications wording of the closest related product

Label matched

Drospirenone (Slynd)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

43,937 reports · 78% serious · 664 with death outcome · 100% female

openFDA FAERS counts, all years, deduplication not applied

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 )

FDA label, Indications and Usage

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.

FDA label, Description section

Boxed warning

None in the current 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 (related wording) 4Reporting / coding artifact 1Lab value / disease marker 1Not in label — unassessed 34
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). 1,093 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
Gallbladder injury1,6162,540.0
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 — unassessedserious n=1,615not reported in cached trials
Biliary dyskinesia1,4282,532.5
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 — unassessedserious n=1,429not reported in cached trials
Cholecystitis chronic5,5332,233.9
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 — unassessedserious PRR 285.4not reported in cached trials
Gallbladder cholesterolosis3591,757.5
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 — unassessedserious n=360not reported in cached trials
Cholesterosis1891,287.3
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 — unassessedserious n=189not reported in cached trials
Post cholecystectomy syndrome1931,067.1
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 — unassessedserious n=193 · 71% consumernot reported in cached trials
Gallbladder non-functioning354777.4
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 — unassessedserious n=352not reported in cached trials
Murphy's sign positive18445.2
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 markerserious n=18not reported in cached trials
Abnormal withdrawal bleeding314253.1
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 — unassessedserious n=67 · 96% consumernot reported in cached trials
Fat intolerance32242.6
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 — unassessedserious n=31not reported in cached trials
Pelvic venous thrombosis458223.0
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 — unassessedserious n=458not reported in cached trials
Hepatobiliary scan abnormal40216.1
148.6–314.2ROR 216.3 · calibrated p 7e-10 ✓
138.6 EB05 106.2 · IC025 +5.2
3/3 methods agree
Reporting / coding artifactserious n=40not reported in cached trials
Fear of disease547209.5
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 — unassessedserious n=546 · 70% consumernot reported in cached trials
Thrombophlebitis superficial919203.6
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 — unassessedserious n=895not reported in cached trials
Transverse sinus thrombosis153193.8
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 — unassessedserious n=153not reported in cached trials
Intracranial venous sinus thrombosis294177.8
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 — unassessedserious n=293not reported in cached trials
Gallbladder disorder4,051139.8
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 — unassessedserious PRR 86.8not reported in cached trials
Withdrawal bleed163137.8
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 — unassessedserious n=60 · 88% consumernot reported in cached trials
Gallbladder pain146134.0
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 — unassessedserious n=144not reported in cached trials
Pulmonary infarction505128.4
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 — unassessedserious n=506not reported in cached trials
Medical diet39117.5
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 — unassessedserious n=39not reported in cached trials
Superior sagittal sinus thrombosis157115.1
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 — unassessedserious n=157not reported in cached trials
Cholecystitis acute1,095114.7
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 — unassessedserious n=1,093not reported in cached trials
Biliary colic535109.3
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 — unassessedserious n=537not reported in cached trials
Ovarian vein thrombosis27104.0
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 — unassessedserious n=27not reported in cached trials
Axillary vein thrombosis6398.4
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 — unassessedserious n=63 · 73% consumernot reported in cached trials
Post thrombotic syndrome7696.3
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 — unassessedserious n=76not reported in cached trials
Iliac vein occlusion1092.1
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 — unassessedserious n=10not reported in cached trials
Cholecystectomy1,78589.0
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 — unassessedserious PRR 56.8not reported in cached trials
Contact lens intolerance2485.4
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 — unassessed78% consumernot reported in cached trials
Injury10,71285.3
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 — unassessedserious PRR 64.0not reported in cached trials
Post gastric surgery syndrome1272.3
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 — unassessedserious n=12not reported in cached trials
Paradoxical embolism1471.5
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 — unassessedserious n=14not reported in cached trials
Cholecystitis1,48968.3
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 — unassessedserious PRR 44.4not reported in cached trials
Cholelithiasis4,10168.2
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 — unassessedserious PRR 46.1not reported in cached trials
Fear of death24859.5
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 — unassessedserious n=248not 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).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Pain12,86910.2
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 11.4not reported in cached trials
Injury10,71285.3
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 — unassessedserious PRR 64.0not reported in cached trials
Anxiety6,89511.8
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 — unassessedserious PRR 12.2not reported in cached trials
Emotional distress6,36126.3
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 — unassessedserious PRR 20.6not reported in cached trials
Cholecystitis chronic5,5332,233.9
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 — unassessedserious PRR 285.4not reported in cached trials
Cholelithiasis4,10168.2
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 — unassessedserious PRR 46.1not reported in cached trials
Gallbladder disorder4,051139.8
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 — unassessedserious PRR 86.8not reported in cached trials
General physical health deterioration3,26713.9
13.5–14.4ROR 15.0 · calibrated p 0.007 ✓
13.6 EB05 13.2 · IC025 +3.7
3/3 methods agree
Reporting / coding artifactserious PRR 11.6not reported in cached trials
Nausea2,9031.8
1.7–1.8ROR 1.8 · calibrated p 0.837
1.8 EB05 1.7 · IC025 +0.8Labeled adverse reaction
exact term
serious PRR 1.9not reported in cached trials
Abdominal pain2,7725.7
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 5.1not reported in cached trials
Dyspnoea (shortness of breath)2,3362.0
1.9–2.1ROR 2.0 · calibrated p 0.960
2.0 EB05 1.9 · IC025 +0.9Not in label — unassessedserious PRR 1.9not reported in cached trials
Anhedonia2,24144.1
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 — unassessedserious PRR 32.8not reported in cached trials
Thrombosis2,03412.3
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 — unassessedserious PRR 9.1not 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.

✓ 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

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.