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Metoprolol side effects: what 252,783 FDA adverse event reports show

Metoprolol · Metoprolol Tartrate · 1,161 reaction terms · 945,446 drug–reaction co-reports · data 2026-09-14
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Drug class

Beta-adrenergic blocker

FDA label, Indications wording

Brand names

Metoprolol Tartrate

openFDA label

Who reports

252,783 reports · 70% serious · 28,672 with death outcome · 53% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

PubChem CID 4171 (ChEBI)

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 adverse reaction 2Labeled (related wording) 5Likely indication confounding 6Reporting / coding artifact 2Lab value / disease marker 1Not 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). 1,121 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
Brash syndrome59564.6
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 — unassessedserious n=595 · 100% clinicianno trial arm names this drug
Ejection fraction23053.6
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 — unassessedserious n=223 · ♀ 100% (drug 53%)no trial arm names this drug
Sensitisation25240.4
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 — unassessedserious n=248 · ♀ 100% (drug 53%)no trial arm names this drug
Nephrogenic anaemia95421.1
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 — unassessedserious n=953no trial arm names this drug
Chronic kidney disease-mineral and bone disorder21420.4
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 — unassessedserious n=214no trial arm names this drug
Hyperparathyroidism secondary50120.3
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 — unassessedserious n=501no trial arm names this drug
Product monitoring error27619.6
17.2–22.3ROR 19.6 · calibrated p 0.002 ✓
15.9 EB05 14.4 · IC025 +3.8
3/3 methods agree
Reporting / coding artifactserious n=276 · 100% clinicianno trial arm names this drug
Polycystic ovaries25115.6
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 — unassessedserious n=251 · ♀ 100% (drug 53%)no trial arm names this drug
Ejection fraction abnormal16212.5
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 markerserious n=148 · ♀ 100% (drug 53%)no trial arm names this drug
Rebound acid hypersecretion39312.1
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 — unassessedserious n=393no trial arm names this drug
End stage renal disease2,05710.3
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 — unassessedserious PRR 7.6no trial arm names this drug
Systemic infection1578.5
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 — unassessedserious n=157 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Haemorrhagic anaemia3968.0
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 — unassessedserious n=396no trial arm names this drug
Atrial flutter6106.8
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 — unassessedserious PRR 5.2no trial arm names this drug
Atrial fibrillation6,8646.2
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 — unassessedage-adj. PRR 4.1 · serious PRR 4.8no trial arm names this drug
Chronic kidney disease5,3776.2
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 4.9no trial arm names this drug
Atrioventricular block first degree2986.0
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 — unassessedserious n=296 · 100% clinicianno trial arm names this drug
Blood pressure diastolic abnormal1746.0
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% clinicianno trial arm names this drug
Coronary artery stenosis3405.9
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 — unassessedserious n=336 · ♀ 33% (drug 53%)no trial arm names this drug
Suspected suicide3215.9
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% clinicianno trial arm names this drug
Coronary artery occlusion9065.8
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 — unassessedserious PRR 4.5no trial arm names this drug
Tachyarrhythmia1625.7
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 — unassessedserious n=162 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Nephrogenic systemic fibrosis1985.7
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 — unassessedserious n=196 · 100% clinicianno trial arm names this drug
Aortic stenosis2225.6
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 — unassessedserious n=220no trial arm names this drug
Labelled drug-drug interaction medication error5675.6
5.1–6.1ROR 5.6 · calibrated p 0.182
5.2 EB05 4.9 · IC025 +2.3
3/3 methods agree
Reporting / coding artifactserious PRR 4.9no trial arm names this drug
Orthopnoea2025.5
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 — unassessedserious n=193 · 100% clinicianno trial arm names this drug
Heart valve incompetence1815.5
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 — unassessedserious n=166 · 100% consumerno trial arm names this drug
Bradycardia (slow heart rate)3,2285.3
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 4.2no trial arm names this drug
Essential hypertension1575.3
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% clinicianno trial arm names this drug
Diastolic dysfunction1865.2
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% clinicianno trial arm names this drug
Coronary artery disease1,7985.1
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 4.0no trial arm names this drug
Lower gastrointestinal haemorrhage4335.1
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 — unassessedserious PRR 4.0no trial arm names this drug
Ventricular hypokinesia1784.8
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 — unassessedserious n=179 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Ischaemic cardiomyopathy1714.8
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% clinicianno trial arm names this drug
Atrioventricular block complete3684.8
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 — unassessedserious n=367 · 100% clinicianno 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.

ConceptReportsPRR 95% CIReading
Arrhythmia / qt9,6264.34.2–4.4signal
Heart failure6,7803.23.2–3.3signal
Myocardial infarction7,4123.13.0–3.2signal
Gi bleeding6,2422.92.8–3.0signal
Kidney injury15,3902.92.8–2.9signal
Anaemia8,0362.32.2–2.3signal
Hyponatraemia2,0932.22.1–2.3signal
Fall / fracture9,8512.22.1–2.2signal
Rhabdomyolysis / myopathy2,0192.12.0–2.2signal
Stroke5,4721.81.8–1.9raised
Hypoglycaemia2,0141.81.7–1.8raised
Serious infection15,8901.71.7–1.7raised
Suicidality5,0491.71.7–1.8raised
Venous thromboembolism4,0561.61.5–1.6raised
Thrombocytopenia3,9371.51.4–1.5raised
Hyperglycaemia / diabetes6,1461.51.4–1.5raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Metoprolol only as a background or rescue medication (NCT00000620, NCT00716079); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

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
Dyspnoea (shortness of breath)14,5062.2
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 1.9no trial arm names this drug
Diarrhoea (diarrhea)14,0881.8
1.8–1.9ROR 1.9 · calibrated p 0.879
1.8 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.6no trial arm names this drug
Nausea13,8471.5
1.4–1.5ROR 1.5 · calibrated p 0.635
1.5 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.5no trial arm names this drug
Drug ineffective (drug did not work)12,9100.8
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 artifactage-adj. PRR 1.0 · serious PRR 1.0no trial arm names this drug
Dizziness12,0242.0
2.0–2.1ROR 2.1 · calibrated p 0.987
2.0 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.0no trial arm names this drug
Off label use (used outside approved label)10,2701.0
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 artifactage-adj. PRR 0.9 · serious PRR 1.0no trial arm names this drug
Death10,0081.0
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 reactionage-adj. PRR 0.9 · serious PRR 0.8no trial arm names this drug
Asthenia (weakness)9,6302.2
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 — unassessedage-adj. PRR 1.7 · serious PRR 1.9no trial arm names this drug
Pain9,3271.3
1.2–1.3ROR 1.3 · calibrated p 0.488
1.3 EB05 1.2 · IC025 +0.3Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.2no trial arm names this drug
Fall9,3192.4
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 — unassessedage-adj. PRR 1.7 · serious PRR 2.1no trial arm names this drug
Headache9,1241.2
1.2–1.2ROR 1.2 · calibrated p 0.453
1.2 EB05 1.2 · IC025 +0.2Labeled adverse reaction
exact term
age-adj. PRR 1.2 · serious PRR 1.2no trial arm names this drug
Hypotension (low blood pressure)7,7393.3
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 2.7no trial arm names this drug
Vomiting7,3741.3
1.3–1.3ROR 1.3 · calibrated p 0.520
1.3 EB05 1.3 · IC025 +0.3Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.2no trial arm names this drug
Pneumonia (lung infection)7,2881.9
1.8–1.9ROR 1.9 · calibrated p 0.897
1.9 EB05 1.8 · IC025 +0.9Not in label — unassessedage-adj. PRR 1.5 · serious PRR 1.6no 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.

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

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.