Metoprolol side effects: what 252,783 FDA adverse event reports show
Drug class
Beta-adrenergic blocker
Brand names
Metoprolol Tartrate
Who reports
252,783 reports · 70% serious · 28,672 with death outcome · 53% female
Used for
Metoprolol tartrate tablet is a beta-adrenergic blocker indicated for the treatment of: • Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) • Angina Pectoris.
What it is
Metoprolol is a propanolamine that is 1-(propan-2-ylamino)propan-2-ol substituted by a 4-(2-methoxyethyl)phenoxy group at position 1. It has a role as a geroprotector, a beta-adrenergic antagonist, an antihypertensive agent, a xenobiotic and an environmental contaminant.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- 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.
- 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). 1,121 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 |
|---|---|---|---|---|---|---|
| Brash syndrome | 595 | 64.6 58.0–72.0ROR 64.8 · calibrated p 3e-6 ✓ | 36.3 EB05 33.9 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=595 · 100% clinician | no trial arm names this drug |
| Ejection fraction | 230 | 53.6 45.4–63.3ROR 53.6 · calibrated p 1e-5 ✓ | 32.5 EB05 29.2 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=223 · ♀ 100% (drug 53%) | no trial arm names this drug |
| Sensitisation | 252 | 40.4 34.7–47.0ROR 40.5 · calibrated p 5e-5 ✓ | 27.2 EB05 24.5 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=248 · ♀ 100% (drug 53%) | no trial arm names this drug |
| Nephrogenic anaemia | 954 | 21.1 19.6–22.6ROR 21.1 · calibrated p 0.002 ✓ | 16.9 EB05 16.0 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=953 | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 214 | 20.4 17.6–23.7ROR 20.4 · calibrated p 0.002 ✓ | 16.5 EB05 14.7 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=214 | no trial arm names this drug |
| Hyperparathyroidism secondary | 501 | 20.3 18.4–22.4ROR 20.3 · calibrated p 0.002 ✓ | 16.4 EB05 15.2 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=501 | no trial arm names this drug |
| Product monitoring error | 276 | 19.6 17.2–22.3ROR 19.6 · calibrated p 0.002 ✓ | 15.9 EB05 14.4 · IC025 +3.8 3/3 methods agree | Reporting / coding artifact | serious n=276 · 100% clinician | no trial arm names this drug |
| Polycystic ovaries | 251 | 15.6 13.6–17.9ROR 15.6 · calibrated p 0.006 ✓ | 13.2 EB05 11.9 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=251 · ♀ 100% (drug 53%) | no trial arm names this drug |
| Hypertensive emergency | 157 | 12.7 10.8–15.1ROR 12.7 · calibrated p 0.014 ✓ | 11.0 EB05 9.6 · IC025 +3.2 3/3 methods agree | Labeled (related wording) related wording | serious n=157 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Ejection fraction abnormal | 162 | 12.5 10.6–14.7ROR 12.5 · calibrated p 0.015 ✓ | 10.8 EB05 9.5 · IC025 +3.1 3/3 methods agree | Lab value / disease marker | serious n=148 · ♀ 100% (drug 53%) | no trial arm names this drug |
| Rebound acid hypersecretion | 393 | 12.1 10.8–13.4ROR 12.1 · calibrated p 0.017 ✓ | 10.6 EB05 9.7 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=393 | no trial arm names this drug |
| End stage renal disease | 2,057 | 10.3 9.9–10.8ROR 10.4 · calibrated p 0.028 ✓ | 9.3 EB05 8.9 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious PRR 7.6 | no trial arm names this drug |
| Systemic infection | 157 | 8.5 7.2–10.1ROR 8.6 · calibrated p 0.056 | 7.7 EB05 6.7 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=157 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Haemorrhagic anaemia | 396 | 8.0 7.2–8.9ROR 8.0 · calibrated p 0.067 | 7.3 EB05 6.7 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=396 | no trial arm names this drug |
| Atrial flutter | 610 | 6.8 6.2–7.3ROR 6.8 · calibrated p 0.109 | 6.3 EB05 5.9 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | serious PRR 5.2 | no trial arm names this drug |
| Rhinitis allergic | 321 | 6.4 5.7–7.2ROR 6.4 · calibrated p 0.128 | 5.9 EB05 5.4 · IC025 +2.4 3/3 methods agree | Labeled (related wording) related wording | serious n=312 · ♀ 100% (drug 53%) | no trial arm names this drug |
| Atrial fibrillation | 6,864 | 6.2 6.1–6.4ROR 6.4 · calibrated p 0.129 | 5.8 EB05 5.7 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | age-adj. PRR 4.1 · serious PRR 4.8 | no trial arm names this drug |
| Chronic kidney disease | 5,377 | 6.2 6.0–6.4ROR 6.3 · calibrated p 0.132 | 5.8 EB05 5.7 · IC025 +2.5 3/3 methods agree | Likely indication confounding term in indications | age-adj. PRR 5.1 · serious PRR 4.9 | no trial arm names this drug |
| Atrioventricular block first degree | 298 | 6.0 5.3–6.8ROR 6.0 · calibrated p 0.150 | 5.6 EB05 5.1 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=296 · 100% clinician | no trial arm names this drug |
| Blood pressure diastolic abnormal | 174 | 6.0 5.1–6.9ROR 6.0 · calibrated p 0.155 | 5.5 EB05 4.9 · IC025 +2.2 3/3 methods agree | Likely indication confounding term in indications | serious n=170 · ♀ 100% (drug 53%) · 100% clinician | no trial arm names this drug |
| Coronary artery stenosis | 340 | 5.9 5.3–6.6ROR 5.9 · calibrated p 0.156 | 5.5 EB05 5.1 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious n=336 · ♀ 33% (drug 53%) | no trial arm names this drug |
| Suspected suicide | 321 | 5.9 5.3–6.6ROR 5.9 · calibrated p 0.156 | 5.5 EB05 5.0 · IC025 +2.3 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=321 · 100% clinician | no trial arm names this drug |
| Coronary artery occlusion | 906 | 5.8 5.4–6.2ROR 5.8 · calibrated p 0.165 | 5.4 EB05 5.1 · IC025 +2.3 3/3 methods agree | Not in label — unassessed | serious PRR 4.5 | no trial arm names this drug |
| Tachyarrhythmia | 162 | 5.7 4.8–6.7ROR 5.7 · calibrated p 0.175 | 5.3 EB05 4.6 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=162 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Nephrogenic systemic fibrosis | 198 | 5.7 4.9–6.5ROR 5.7 · calibrated p 0.175 | 5.3 EB05 4.7 · IC025 +2.2 3/3 methods agree | Not in label — unassessed | serious n=196 · 100% clinician | no trial arm names this drug |
| Aortic stenosis | 222 | 5.6 4.9–6.4ROR 5.6 · calibrated p 0.182 | 5.2 EB05 4.7 · IC025 +2.2 3/3 methods agree | Not in label — unassessed | serious n=220 | no trial arm names this drug |
| Labelled drug-drug interaction medication error | 567 | 5.6 5.1–6.1ROR 5.6 · calibrated p 0.182 | 5.2 EB05 4.9 · IC025 +2.3 3/3 methods agree | Reporting / coding artifact | serious PRR 4.9 | no trial arm names this drug |
| Orthopnoea | 202 | 5.5 4.8–6.4ROR 5.5 · calibrated p 0.185 | 5.2 EB05 4.6 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=193 · 100% clinician | no trial arm names this drug |
| Angina unstable | 415 | 5.5 5.0–6.1ROR 5.5 · calibrated p 0.184 | 5.2 EB05 4.8 · IC025 +2.2 3/3 methods agree | Labeled (related wording) related wording | serious n=414 | no trial arm names this drug |
| Heart valve incompetence | 181 | 5.5 4.7–6.4ROR 5.5 · calibrated p 0.189 | 5.2 EB05 4.6 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious n=166 · 100% consumer | no trial arm names this drug |
| Bradycardia (slow heart rate) | 3,228 | 5.3 5.1–5.5ROR 5.4 · calibrated p 0.199 | 5.0 EB05 4.9 · IC025 +2.3 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 4.3 · serious PRR 4.2 | no trial arm names this drug |
| Essential hypertension | 157 | 5.3 4.5–6.2ROR 5.3 · calibrated p 0.208 | 5.0 EB05 4.3 · IC025 +2.0 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=151 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Diastolic dysfunction | 186 | 5.2 4.5–6.1ROR 5.2 · calibrated p 0.213 | 4.9 EB05 4.3 · IC025 +2.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=184 · 100% clinician | no trial arm names this drug |
| Sinus bradycardia | 578 | 5.2 4.8–5.7ROR 5.2 · calibrated p 0.213 | 4.9 EB05 4.6 · IC025 +2.2 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 4.2 · serious PRR 4.2 · 100% clinician | no trial arm names this drug |
| Cardiac failure chronic | 252 | 5.2 4.5–5.9ROR 5.2 · calibrated p 0.219 | 4.9 EB05 4.4 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious n=251 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Coronary artery disease | 1,798 | 5.1 4.9–5.4ROR 5.2 · calibrated p 0.218 | 4.9 EB05 4.7 · IC025 +2.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.0 | no trial arm names this drug |
| Lower gastrointestinal haemorrhage | 433 | 5.1 4.6–5.6ROR 5.1 · calibrated p 0.226 | 4.8 EB05 4.4 · IC025 +2.1 3/3 methods agree | Not in label — unassessed | serious PRR 4.0 | no trial arm names this drug |
| Ventricular hypokinesia | 178 | 4.8 4.1–5.6ROR 4.8 · calibrated p 0.260 | 4.5 EB05 4.0 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious n=179 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Ischaemic cardiomyopathy | 171 | 4.8 4.1–5.6ROR 4.8 · calibrated p 0.261 | 4.5 EB05 4.0 · IC025 +1.9 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=172 · ♀ 0% (drug 53%) · 100% clinician | no trial arm names this drug |
| Atrioventricular block complete | 368 | 4.8 4.3–5.3ROR 4.8 · calibrated p 0.260 | 4.5 EB05 4.2 · IC025 +2.0 3/3 methods agree | Not in label — unassessed | serious n=367 · 100% clinician | no trial arm names this drug |
Clinical concept groups
MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Arrhythmia / qt | 9,626 | 4.34.2–4.4 | signal |
| Heart failure | 6,780 | 3.23.2–3.3 | signal |
| Myocardial infarction | 7,412 | 3.13.0–3.2 | signal |
| Gi bleeding | 6,242 | 2.92.8–3.0 | signal |
| Kidney injury | 15,390 | 2.92.8–2.9 | signal |
| Anaemia | 8,036 | 2.32.2–2.3 | signal |
| Hyponatraemia | 2,093 | 2.22.1–2.3 | signal |
| Fall / fracture | 9,851 | 2.22.1–2.2 | signal |
| Rhabdomyolysis / myopathy | 2,019 | 2.12.0–2.2 | signal |
| Stroke | 5,472 | 1.81.8–1.9 | raised |
| Hypoglycaemia | 2,014 | 1.81.7–1.8 | raised |
| Serious infection | 15,890 | 1.71.7–1.7 | raised |
| Suicidality | 5,049 | 1.71.7–1.8 | raised |
| Venous thromboembolism | 4,056 | 1.61.5–1.6 | raised |
| Thrombocytopenia | 3,937 | 1.51.4–1.5 | raised |
| Hyperglycaemia / diabetes | 6,146 | 1.51.4–1.5 | raised |
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 |
|---|---|---|---|---|---|---|
| Fatigue (tiredness) | 16,481 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.848 | 1.8 EB05 1.7 · IC025 +0.8 | Labeled (related wording) related wording | age-adj. PRR 1.5 · serious PRR 1.8 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 14,506 | 2.2 2.1–2.2ROR 2.2 · calibrated p 0.938 | 2.1 EB05 2.1 · IC025 +1.1 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 1.8 · serious PRR 1.9 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 14,088 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.879 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.6 | no trial arm names this drug |
| Nausea | 13,847 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.635 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.5 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 12,910 | 0.8 0.8–0.8ROR 0.8 · calibrated p 0.184 | 0.8 EB05 0.8 · IC025 -0.3 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 1.0 · serious PRR 1.0 | no trial arm names this drug |
| Dizziness | 12,024 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.987 | 2.0 EB05 2.0 · IC025 +1.0 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 2.0 | no trial arm names this drug |
| Off label use (used outside approved label) | 10,270 | 1.0 1.0–1.0ROR 1.0 · calibrated p 0.294 | 1.0 EB05 1.0 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 0.9 · serious PRR 1.0 | no trial arm names this drug |
| Death | 10,008 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.282 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Outcome field, not a reaction | age-adj. PRR 0.9 · serious PRR 0.8 | no trial arm names this drug |
| Asthenia (weakness) | 9,630 | 2.2 2.1–2.2ROR 2.2 · calibrated p 0.952 | 2.1 EB05 2.1 · IC025 +1.1 3/3 methods agree | Not in label — unassessed | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
| Pain | 9,327 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.488 | 1.3 EB05 1.2 · IC025 +0.3 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.2 | no trial arm names this drug |
| Fall | 9,319 | 2.4 2.3–2.4ROR 2.4 · calibrated p 0.850 | 2.3 EB05 2.3 · IC025 +1.2 3/3 methods agree | Not in label — unassessed | age-adj. PRR 1.7 · serious PRR 2.1 | no trial arm names this drug |
| Headache | 9,124 | 1.2 1.2–1.2ROR 1.2 · calibrated p 0.453 | 1.2 EB05 1.2 · IC025 +0.2 | Labeled adverse reaction exact term | age-adj. PRR 1.2 · serious PRR 1.2 | no trial arm names this drug |
| Hypotension (low blood pressure) | 7,739 | 3.3 3.2–3.4ROR 3.4 · calibrated p 0.519 | 3.2 EB05 3.1 · IC025 +1.6 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 2.6 · serious PRR 2.7 | no trial arm names this drug |
| Vomiting | 7,374 | 1.3 1.3–1.3ROR 1.3 · calibrated p 0.520 | 1.3 EB05 1.3 · IC025 +0.3 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.2 | no trial arm names this drug |
| Pneumonia (lung infection) | 7,288 | 1.9 1.8–1.9ROR 1.9 · calibrated p 0.897 | 1.9 EB05 1.8 · IC025 +0.9 | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.6 | no trial arm names this drug |
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.
- Brash syndrome — n=595, PRR 64.6
- Ejection fraction — n=230, PRR 53.6
- Sensitisation — n=252, PRR 40.4
- Nephrogenic anaemia — n=954, PRR 21.1
- Chronic kidney disease-mineral and bone disorder — n=214, PRR 20.4
- Hyperparathyroidism secondary — n=501, PRR 20.3
- Polycystic ovaries — n=251, PRR 15.6
- Rebound acid hypersecretion — n=393, PRR 12.1
- End stage renal disease — n=2,057, PRR 10.3
- Systemic infection — n=157, PRR 8.5
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 Metoprolol?
In FDA FAERS, the most frequently co-reported reaction terms for Metoprolol are fatigue, dyspnoea, diarrhoea, nausea, dizziness, asthenia. 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 Metoprolol have an FDA boxed warning?
No. The FDA label retrieved for Metoprolol has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Metoprolol 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 00940cc5-d2eb-4841-9138-de97d7b1c674, effective 20260727; matched on
openfda.generic_name.exact:"METOPROLOL" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 4171 description (ChEBI)
- 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, 1,161 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
METOPROLOL, 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.