Secnidazole side effects: what 281 FDA adverse event reports show
Drug class
Brand names
Solosec
Who reports
281 reports · 23% serious · 3 with death outcome · 92% female
Used for
SOLOSEC ® is a nitroimidazole antimicrobial indicated for: Treatment of bacterial vaginosis in female patients 12 years of age and older. ( 1.1 ) Treatment of trichomoniasis in patients 12 years of age and older. ( 1.2 ) To reduce the development of dr.
What it is
The active ingredient in SOLOSEC Oral Granules is secnidazole (also named 1-(2-hydroxypropyl)-2-methyl-5-nitroimidazole and 1-(2-methyl-5-nitro-1 H -imidazol-1-yl) propan-2-ol), a nitroimidazole antimicrobial.
Boxed warning
None in the current label
Causality screen of the 5 strongest signals
What the badges mean
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- 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.
- 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 flags pairs whose reports are unusually skewed by sex or come mostly from consumers rather than clinicians. 1 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 |
|---|---|---|---|---|---|---|
| Product taste abnormal | 21 | 116.7 77.3–176.1ROR 126.0 · χ² 2,292 / p <1e-300 | 105.6 EB05 72.8 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | serious n=1 | no trial data cached |
| Vaginal discharge | 9 | 66.9 35.2–127.3ROR 69.1 · χ² 520 / p 2e-115 | 58.9 EB05 33.2 · IC025 +2.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=1 | no trial data cached |
| Chromaturia | 11 | 36.4 20.4–64.9ROR 37.8 · χ² 344 / p 5e-77 | 34.4 EB05 20.4 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious PRR 39.0 | no trial data cached |
| Premature delivery | 6 | 28.0 12.7–61.8ROR 28.6 · χ² 130 / p 2e-30 | 25.0 EB05 10.8 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious PRR 71.4 | no trial data cached |
| Hair texture abnormal | 5 | 27.7 11.6–65.9ROR 28.1 · χ² 103 / p 1e-24 | 23.5 EB05 8.2 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=5 | no trial data cached |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Product taste abnormal | 21 | 116.7 77.3–176.1ROR 126.0 · χ² 2,292 / p <1e-300 | 105.6 EB05 72.8 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | serious n=1 | no trial data cached |
| Chromaturia | 11 | 36.4 20.4–64.9ROR 37.8 · χ² 344 / p 5e-77 | 34.4 EB05 20.4 · IC025 +2.8 3/3 methods agree | Not in label — unassessed | serious PRR 39.0 | no trial data cached |
| Vaginal discharge | 9 | 66.9 35.2–127.3ROR 69.1 · χ² 520 / p 2e-115 | 58.9 EB05 33.2 · IC025 +2.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=1 | no trial data cached |
| Premature delivery | 6 | 28.0 12.7–61.8ROR 28.6 · χ² 130 / p 2e-30 | 25.0 EB05 10.8 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious PRR 71.4 | no trial data cached |
| Hair texture abnormal | 5 | 27.7 11.6–65.9ROR 28.1 · χ² 103 / p 1e-24 | 23.5 EB05 8.2 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious n=5 | no trial data cached |
| Hepatic cytolysis | 3 | 18.3 5.9–56.5ROR 18.5 · χ² 33 / p 4e-9 | 10.1 EB05 2.5 · IC025 +0.3 3/3 methods agree | Not in label — unassessed | serious PRR 45.6 | no trial data cached |
Unlabeled candidate signals
Every screened signal with n ≥ 20 was either labeled, an indication term, or an artifact pattern — no unlabeled candidate stood out in the top signals.
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 Secnidazole?
In FDA FAERS, the most frequently co-reported reaction terms for Secnidazole are chromaturia, vaginal discharge, premature delivery, hair texture abnormal, hepatic cytolysis. 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 Secnidazole have an FDA boxed warning?
No. The FDA label retrieved for Secnidazole has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Secnidazole 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 056485b6-8bba-4a21-ae00-cdb4e7ae4bfa, effective 20250219; matched on
openfda.generic_name.exact:"SECNIDAZOLE") - 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, 6 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
Page generated 2026-10-08. 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.