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Metoprolol Tartrate Injection side effects: what 188,514 FDA adverse event reports show

Metoprolol Tartrate Injection · Metoprolol Tartrate · 1,159 reaction terms · 703,978 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

188,514 reports · 71% serious · 21,366 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 2Not in label — unassessed 23
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). 1,119 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
Ejection fraction21665.1
55.0–77.0ROR 65.1 · calibrated p 3e-6 ✓
40.9 EB05 36.6 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=210 · ♀ 100% (drug 53%)no trial arm names this drug
Brash syndrome45856.5
50.5–63.3ROR 56.7 · calibrated p 6e-6 ✓
37.5 EB05 34.7 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=458 · 100% clinicianno trial arm names this drug
Sensitisation24050.6
43.4–58.9ROR 50.6 · calibrated p 1e-5 ✓
34.8 EB05 31.2 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=237 · ♀ 100% (drug 53%)no trial arm names this drug
Product monitoring error27025.6
22.4–29.2ROR 25.7 · calibrated p 6e-4 ✓
20.9 EB05 18.9 · IC025 +4.1
3/3 methods agree
Reporting / coding artifactserious n=270 · 100% clinicianno trial arm names this drug
Nephrogenic anaemia72620.3
18.8–22.0ROR 20.4 · calibrated p 0.002 ✓
17.3 EB05 16.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=725no trial arm names this drug
Polycystic ovaries24120.0
17.4–22.9ROR 20.0 · calibrated p 0.002 ✓
17.0 EB05 15.3 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=241 · ♀ 100% (drug 53%)no trial arm names this drug
Hyperparathyroidism secondary37319.1
17.1–21.3ROR 19.1 · calibrated p 0.002 ✓
16.4 EB05 15.0 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=373no trial arm names this drug
Chronic kidney disease-mineral and bone disorder14717.5
14.7–20.8ROR 17.5 · calibrated p 0.004 ✓
15.1 EB05 13.2 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=147no trial arm names this drug
Ejection fraction abnormal14514.8
12.4–17.6ROR 14.8 · calibrated p 0.008 ✓
13.1 EB05 11.3 · IC025 +3.4
3/3 methods agree
Lab value / disease markerserious n=133no trial arm names this drug
Rebound acid hypersecretion30112.0
10.7–13.5ROR 12.0 · calibrated p 0.017 ✓
10.9 EB05 9.9 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=301no trial arm names this drug
Systemic infection14910.9
9.2–12.8ROR 10.9 · calibrated p 0.025 ✓
9.8 EB05 8.6 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=149 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
End stage renal disease1,60610.5
10.0–11.1ROR 10.6 · calibrated p 0.026 ✓
9.7 EB05 9.3 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious PRR 7.9no trial arm names this drug
Haemorrhagic anaemia3108.2
7.3–9.2ROR 8.3 · calibrated p 0.061
7.7 EB05 7.0 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=310 · 73% consumerno trial arm names this drug
Suspected suicide3187.9
7.0–8.8ROR 7.9 · calibrated p 0.070
7.4 EB05 6.7 · IC025 +2.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=318 · 100% clinicianno trial arm names this drug
Labelled drug-drug interaction medication error5327.0
6.4–7.6ROR 7.0 · calibrated p 0.099
6.6 EB05 6.1 · IC025 +2.6
3/3 methods agree
Reporting / coding artifactserious PRR 6.1no trial arm names this drug
Blood pressure diastolic abnormal1466.6
5.6–7.8ROR 6.6 · calibrated p 0.117
6.2 EB05 5.4 · IC025 +2.4
3/3 methods agree
Likely indication confounding
term in indications
serious n=142 · ♀ 100% (drug 53%) · 100% clinicianno trial arm names this drug
Chronic kidney disease4,2816.5
6.3–6.7ROR 6.7 · calibrated p 0.114
6.2 EB05 6.1 · IC025 +2.6
3/3 methods agree
Likely indication confounding
term in indications
age-adj. PRR 5.2 · serious PRR 5.1no trial arm names this drug
Atrial flutter4266.2
5.6–6.8ROR 6.2 · calibrated p 0.138
5.9 EB05 5.4 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious PRR 4.9no trial arm names this drug
Clostridium test positive1146.1
5.0–7.3ROR 6.1 · calibrated p 0.148
5.7 EB05 4.9 · IC025 +2.2
3/3 methods agree
Lab value / disease markerserious n=113 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Atrial fibrillation5,0766.1
5.9–6.2ROR 6.2 · calibrated p 0.138
5.8 EB05 5.7 · IC025 +2.5
3/3 methods agree
Not in label — unassessedage-adj. PRR 4.0 · serious PRR 4.7no trial arm names this drug
Pericardial haemorrhage1125.9
4.9–7.2ROR 5.9 · calibrated p 0.157
5.6 EB05 4.7 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=112 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Heart valve incompetence1415.7
4.8–6.7ROR 5.7 · calibrated p 0.175
5.4 EB05 4.7 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious n=127 · 100% consumerno trial arm names this drug
Coronary artery occlusion6745.7
5.2–6.1ROR 5.7 · calibrated p 0.173
5.4 EB05 5.1 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious PRR 4.4no trial arm names this drug
Coronary artery stenosis2465.7
5.0–6.4ROR 5.7 · calibrated p 0.176
5.4 EB05 4.8 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=243 · ♀ 30% (drug 53%)no trial arm names this drug
Tachyarrhythmia1215.6
4.7–6.7ROR 5.6 · calibrated p 0.181
5.3 EB05 4.5 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious n=121 · ♀ 0% (drug 53%) · 100% clinicianno trial arm names this drug
Atrioventricular block first degree2045.4
4.7–6.2ROR 5.4 · calibrated p 0.196
5.1 EB05 4.6 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious n=205 · 100% clinicianno trial arm names this drug
Anti-neutrophil cytoplasmic antibody positive vasculitis1135.4
4.4–6.5ROR 5.4 · calibrated p 0.203
5.1 EB05 4.3 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious n=113 · ♀ 100% (drug 53%) · 100% clinicianno trial arm names this drug
Diastolic dysfunction1435.3
4.5–6.3ROR 5.3 · calibrated p 0.205
5.0 EB05 4.4 · IC025 +2.1
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=141 · 100% clinicianno trial arm names this drug
Blood pressure systolic abnormal1145.3
4.4–6.4ROR 5.3 · calibrated p 0.209
5.0 EB05 4.3 · IC025 +2.0
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=103 · 100% clinicianno trial arm names this drug
Bradycardia (slow heart rate)2,3525.1
4.9–5.3ROR 5.2 · calibrated p 0.218
4.9 EB05 4.8 · IC025 +2.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.0 · serious PRR 4.1no trial arm names this drug
Aortic stenosis1515.0
4.2–5.9ROR 5.0 · calibrated p 0.238
4.8 EB05 4.1 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious n=150no trial arm names this drug
Lower gastrointestinal haemorrhage3215.0
4.5–5.6ROR 5.0 · calibrated p 0.237
4.8 EB05 4.4 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious PRR 3.9no trial arm names this drug
Coronary artery disease1,3185.0
4.7–5.3ROR 5.0 · calibrated p 0.234
4.8 EB05 4.6 · IC025 +2.2
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.9no trial arm names this drug
Orthopnoea1354.9
4.1–5.8ROR 4.9 · calibrated p 0.252
4.6 EB05 4.0 · IC025 +1.9
3/3 methods agree
Not in label — unassessedserious n=132 · 100% clinicianno trial arm names this drug
Ischaemic cardiomyopathy1284.8
4.0–5.7ROR 4.8 · calibrated p 0.266
4.5 EB05 3.9 · IC025 +1.9
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=129 · ♀ 0% (drug 53%) · 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 / qt7,1744.24.1–4.3signal
Heart failure4,9853.23.1–3.2signal
Myocardial infarction5,5223.13.0–3.1signal
Gi bleeding4,7803.02.9–3.0signal
Kidney injury11,5672.92.8–2.9signal
Anaemia6,0082.32.2–2.3signal
Fall / fracture7,4302.22.1–2.2signal
Hyponatraemia1,5592.22.1–2.3signal
Rhabdomyolysis / myopathy1,5022.12.0–2.2raised
Suicidality4,0911.91.8–1.9raised
Stroke4,0911.81.8–1.9raised
Hypoglycaemia1,4991.81.7–1.8raised
Serious infection11,5191.71.6–1.7raised
Venous thromboembolism2,9331.51.5–1.6raised
Thrombocytopenia2,8181.41.4–1.5raised
Hyperglycaemia / diabetes4,3231.41.4–1.4raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Metoprolol Tartrate Injection 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)10,9222.2
2.1–2.2ROR 2.2 · calibrated p 0.931
2.1 EB05 2.1 · IC025 +1.1
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 2.0no trial arm names this drug
Diarrhoea (diarrhea)10,3101.8
1.8–1.8ROR 1.8 · calibrated p 0.854
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
Nausea10,2021.4
1.4–1.5ROR 1.5 · calibrated p 0.621
1.4 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)10,0930.9
0.8–0.9ROR 0.8 · calibrated p 0.208
0.9 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
Dizziness9,1082.1
2.0–2.1ROR 2.1 · calibrated p 0.999
2.0 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 2.0no trial arm names this drug
Off label use (used outside approved label)8,0371.0
1.0–1.1ROR 1.0 · calibrated p 0.327
1.0 EB05 1.0 · IC025 +0.0Reporting / coding artifactage-adj. PRR 1.0 · serious PRR 1.0no trial arm names this drug
Death7,0340.9
0.9–0.9ROR 0.9 · calibrated p 0.245
0.9 EB05 0.9 · IC025 -0.2
PRR-only: not supported by EBGM or IC
Outcome field, not a reactionage-adj. PRR 0.8 · serious PRR 0.7no trial arm names this drug
Fall7,0222.4
2.3–2.4ROR 2.4 · calibrated p 0.843
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
Asthenia (weakness)6,9562.1
2.0–2.1ROR 2.1 · calibrated p 0.993
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Not in label — unassessedage-adj. PRR 1.6 · serious PRR 1.8no trial arm names this drug
Pain6,8401.2
1.2–1.3ROR 1.2 · calibrated p 0.473
1.2 EB05 1.2 · IC025 +0.3Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.2no trial arm names this drug
Headache6,7881.2
1.2–1.2ROR 1.2 · calibrated p 0.451
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)5,8263.3
3.2–3.4ROR 3.4 · calibrated p 0.516
3.2 EB05 3.2 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.6 · serious PRR 2.7no trial arm names this drug
Vomiting5,5241.3
1.3–1.3ROR 1.3 · calibrated p 0.524
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
Acute kidney injury (sudden kidney damage)5,2954.0
3.9–4.1ROR 4.1 · calibrated p 0.367
3.9 EB05 3.8 · IC025 +1.9
3/3 methods agree
Not in label — unassessedage-adj. PRR 2.3 · serious PRR 3.1no 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.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Pimavanserin Tartrate ↔ Hallucination.

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 Tartrate Injection?

In FDA FAERS, the most frequently co-reported reaction terms for Metoprolol Tartrate Injection are fatigue, dyspnoea, diarrhoea, nausea, dizziness, fall. 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 Tartrate Injection have an FDA boxed warning?

No. The FDA label retrieved for Metoprolol Tartrate Injection has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Metoprolol Tartrate Injection 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.