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Carvedilol side effects: what 134,417 FDA adverse event reports show

Carvedilol · 1,184 reaction terms · 499,763 drug–reaction co-reports · data 2026-09-14
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Drug class

alpha-Adrenergic Blocker, beta-Adrenergic Blocker

FDA label (Established Pharmacologic Class) · compare the class

Who reports

134,417 reports · 70% serious · 16,351 with death outcome · 47% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Carvedilol tablets are an alpha/beta-adrenergic blocking agent indicated for the treatment of: mild to severe chronic heart failure ( 1.1 ) left ventricular dysfunction following myocardial infarction in clinically stable patients( 1.2 ) hypertension( .

FDA label, Indications and Usage

What it is

Carvedilol is a member of the class of carbazoles that is an adrenergic antagonist with non-selective beta- and alpha-1 receptor blocking properties which helps in the management of congestive heart failure.

PubChem CID 2585 (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 (related wording) 5Likely indication confounding 10Reporting / coding artifact 1Lab value / disease marker 4Not in label — unassessed 20
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). 1,144 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
Nephrogenic anaemia92538.3
35.7–41.2ROR 38.6 · calibrated p 7e-5 ✓
30.8 EB05 29.2 · IC025 +4.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=925not reported in cached trials
Hyperparathyroidism secondary49738.0
34.4–41.9ROR 38.1 · calibrated p 7e-5 ✓
30.6 EB05 28.4 · IC025 +4.7
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=496 · 100% cliniciannot reported in cached trials
Brash syndrome26637.9
33.1–43.3ROR 38.0 · calibrated p 8e-5 ✓
30.5 EB05 27.6 · IC025 +4.7
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=266 · 100% cliniciannot reported in cached trials
Chronic kidney disease-mineral and bone disorder21037.7
32.4–43.8ROR 37.7 · calibrated p 8e-5 ✓
30.4 EB05 27.1 · IC025 +4.6
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=210not reported in cached trials
Ischaemic cardiomyopathy37621.4
19.3–23.9ROR 21.5 · calibrated p 0.001 ✓
18.9 EB05 17.4 · IC025 +4.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=376 · ♀ 24% (drug 47%)not reported in cached trials
Cardioactive drug level increased15420.4
17.2–24.1ROR 20.4 · calibrated p 0.002 ✓
18.0 EB05 15.8 · IC025 +3.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Lab value / disease markerserious n=152 · 100% cliniciannot reported in cached trials
Dyspnoea paroxysmal nocturnal8119.1
15.2–24.1ROR 19.2 · calibrated p 0.003 ✓
17.1 EB05 14.1 · IC025 +3.6
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=79 · ♀ 0% (drug 47%)not reported in cached trials
Rebound acid hypersecretion30717.3
15.3–19.4ROR 17.3 · calibrated p 0.004 ✓
15.6 EB05 14.2 · IC025 +3.7
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=307not reported in cached trials
Implantable defibrillator insertion12816.7
13.9–20.1ROR 16.7 · calibrated p 0.005 ✓
15.1 EB05 13.0 · IC025 +3.6
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=125 · 100% consumernot reported in cached trials
End stage renal disease1,75516.3
15.6–17.2ROR 16.5 · calibrated p 0.005 ✓
14.9 EB05 14.3 · IC025 +3.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious PRR 12.2not reported in cached trials
Left atrial dilatation11515.3
12.6–18.5ROR 15.3 · calibrated p 0.007 ✓
13.9 EB05 11.9 · IC025 +3.4
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=115 · 100% cliniciannot reported in cached trials
Orthopnoea27114.4
12.7–16.3ROR 14.4 · calibrated p 0.008 ✓
13.2 EB05 11.9 · IC025 +3.5
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=263not reported in cached trials
Haemorrhagic anaemia35513.4
12.0–15.0ROR 13.4 · calibrated p 0.011 ✓
12.4 EB05 11.3 · IC025 +3.4
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=355not reported in cached trials
Carotid arteriosclerosis7712.6
10.0–15.9ROR 12.6 · calibrated p 0.015 ✓
11.5 EB05 9.5 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=77 · ♀ 0% (drug 47%) · 100% cliniciannot reported in cached trials
N-terminal prohormone brain natriuretic peptide increased10312.3
10.1–15.0ROR 12.3 · calibrated p 0.016 ✓
11.3 EB05 9.5 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Lab value / disease markerserious n=98 · ♀ 0% (drug 47%) · 100% cliniciannot reported in cached trials
Product monitoring error9911.5
9.4–14.1ROR 11.5 · calibrated p 0.021 ✓
10.6 EB05 8.9 · IC025 +3.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Reporting / coding artifactserious n=99 · ♀ 0% (drug 47%) · 100% cliniciannot reported in cached trials
Echocardiogram abnormal9311.1
9.0–13.7ROR 11.1 · calibrated p 0.024 ✓
10.2 EB05 8.5 · IC025 +3.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Lab value / disease markerserious n=87 · ♀ 0% (drug 47%) · 100% consumernot reported in cached trials
Renal artery stenosis9211.0
8.9–13.6ROR 11.0 · calibrated p 0.024 ✓
10.2 EB05 8.5 · IC025 +3.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=92 · 100% cliniciannot reported in cached trials
Left ventricular hypertrophy28110.9
9.6–12.3ROR 10.9 · calibrated p 0.024 ✓
10.2 EB05 9.2 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=277not reported in cached trials
Congestive cardiomyopathy27710.9
9.6–12.3ROR 10.9 · calibrated p 0.024 ✓
10.2 EB05 9.2 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=275not reported in cached trials
Diastolic dysfunction20210.8
9.4–12.5ROR 10.8 · calibrated p 0.025 ✓
10.1 EB05 8.9 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=197not reported in cached trials
Ejection fraction decreased95210.1
9.5–10.8ROR 10.2 · calibrated p 0.031 ✓
9.5 EB05 9.0 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: PRR 167.2 (110.6–252.8)
Likely indication confounding
term in indications
age-adj. PRR 8.8 · serious PRR 7.9not reported in cached trials
Mitral valve incompetence6719.8
9.0–10.6ROR 9.8 · calibrated p 0.035 ✓
9.2 EB05 8.6 · IC025 +3.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedage-adj. PRR 8.0 · serious PRR 7.7not reported in cached trials
Essential hypertension1499.5
8.0–11.2ROR 9.5 · calibrated p 0.040 ✓
8.8 EB05 7.7 · IC025 +2.9
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
term in indications
serious n=143not reported in cached trials
Aortic valve incompetence2339.0
7.8–10.2ROR 9.0 · calibrated p 0.047 ✓
8.4 EB05 7.5 · IC025 +2.9
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=234not reported in cached trials
Chronic kidney disease4,0578.7
8.4–8.9ROR 8.9 · calibrated p 0.047 ✓
8.2 EB05 8.0 · IC025 +3.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedage-adj. PRR 7.8 · serious PRR 6.9not reported in cached trials
Cardiomyopathy7828.7
8.1–9.3ROR 8.7 · calibrated p 0.051
8.2 EB05 7.7 · IC025 +2.9
3/3 methods agree
vs other alpha-Adrenergic Blockers: PRR 197.4 (120.4–323.8)
Likely indication confounding
shares a disease stem with the indications wording
age-adj. PRR 7.9 · serious PRR 6.8not reported in cached trials
Tricuspid valve incompetence4078.4
7.6–9.3ROR 8.4 · calibrated p 0.057
8.0 EB05 7.3 · IC025 +2.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious PRR 6.6not reported in cached trials
Left ventricular dysfunction3378.3
7.4–9.2ROR 8.3 · calibrated p 0.061
7.8 EB05 7.1 · IC025 +2.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
term in indications; also in warnings
serious n=331not reported in cached trials
Dilatation ventricular1078.2
6.8–10.0ROR 8.2 · calibrated p 0.064
7.7 EB05 6.5 · IC025 +2.6
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=107not reported in cached trials
Brain natriuretic peptide increased1548.2
6.9–9.6ROR 8.2 · calibrated p 0.064
7.7 EB05 6.7 · IC025 +2.7
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Lab value / disease markerserious n=143not reported in cached trials
Cardiomegaly6148.1
7.4–8.8ROR 8.1 · calibrated p 0.064
7.7 EB05 7.2 · IC025 +2.8
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Likely indication confounding
shares a disease stem with the indications wording
age-adj. PRR 7.1 · serious PRR 6.5not reported in cached trials
Therapeutic agent toxicity1668.0
6.8–9.4ROR 8.0 · calibrated p 0.068
7.5 EB05 6.6 · IC025 +2.7
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=165not reported in cached trials
Mitral valve disease878.0
6.4–9.9ROR 8.0 · calibrated p 0.070
7.4 EB05 6.2 · IC025 +2.5
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=86 · ♀ 0% (drug 47%) · 100% cliniciannot reported in cached trials
Aortic arteriosclerosis1227.7
6.4–9.2ROR 7.7 · calibrated p 0.077
7.2 EB05 6.2 · IC025 +2.5
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedserious n=120not reported in cached trials

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
Heart failure7,9687.27.1–7.4signal
Kidney injury10,9553.83.7–3.9signal
Gi bleeding4,2093.73.5–3.8signal
Myocardial infarction4,6323.63.5–3.7signal
Arrhythmia / qt4,1683.43.3–3.5signal
Hypoglycaemia1,5492.52.4–2.7signal
Anaemia4,7762.52.4–2.6signal
Hyponatraemia1,1692.32.2–2.4signal
Stroke3,2252.02.0–2.1raised
Fall / fracture4,7111.91.9–2.0raised
Hyperglycaemia / diabetes4,1841.91.8–2.0raised
Serious infection8,4591.71.7–1.8raised
Thrombocytopenia2,1691.51.5–1.6raised
Rhabdomyolysis / myopathy7971.51.4–1.6raised
Venous thromboembolism1,8901.41.3–1.4raised
Pancreatitis6501.31.2–1.4raised

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Carvedilol 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 (3 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
Fatigue (tiredness)8,9131.8
1.8–1.8ROR 1.9 · calibrated p 0.862
1.8 EB05 1.8 · IC025 +0.8
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.7NCT00347360: 2/42 (4.8%) on Carvedilol; 1/43 (2.3%) control
Dyspnoea (shortness of breath)8,3932.3
2.3–2.4ROR 2.4 · calibrated p 0.846
2.3 EB05 2.3 · IC025 +1.2
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.9 · serious PRR 2.1NCT00347360: 1/42 (2.4%) on Carvedilol; 1/44 (2.3%) control
Diarrhoea (diarrhea)7,1441.7
1.7–1.8ROR 1.8 · calibrated p 0.819
1.7 EB05 1.7 · IC025 +0.8
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.5NCT00347360: 1/42 (2.4%) on Carvedilol; 1/43 (2.3%) control
Dizziness6,9682.2
2.1–2.3ROR 2.3 · calibrated p 0.919
2.2 EB05 2.1 · IC025 +1.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: PRR 91.1 (81.3–102.0)
Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 2.0NCT00347360: 4/44 (9.1%) on Carvedilol; 3/43 (7.0%) control
Nausea6,7081.3
1.3–1.4ROR 1.3 · calibrated p 0.539
1.3 EB05 1.3 · IC025 +0.4
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.4NCT00347360: 1/42 (2.4%) on Carvedilol (serious AE)
Drug ineffective (drug did not work)5,8360.7
0.7–0.7ROR 0.7 · calibrated p 0.118
0.7 EB05 0.7 · IC025 -0.6
PRR-only: not supported by EBGM or IC
vs other alpha-Adrenergic Blockers: only this drug
Reporting / coding artifactage-adj. PRR 0.8 · serious PRR 0.8not reported in cached trials
Death5,8051.1
1.0–1.1ROR 1.1 · calibrated p 0.342
1.1 EB05 1.0 · IC025 +0.0
vs other alpha-Adrenergic Blockers: only this drug
Outcome field, not a reactionage-adj. PRR 0.9 · serious PRR 0.9not reported in cached trials
Hypotension (low blood pressure)5,6984.5
4.4–4.7ROR 4.7 · calibrated p 0.270
4.4 EB05 4.3 · IC025 +2.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: PRR 94.3 (83.0–107.1)
Labeled adverse reaction
exact term
age-adj. PRR 3.5 · serious PRR 3.5not reported in cached trials
Asthenia (weakness)5,4662.3
2.2–2.3ROR 2.3 · calibrated p 0.884
2.3 EB05 2.2 · IC025 +1.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 2.0not reported in cached trials
Off label use (used outside approved label)4,6260.8
0.8–0.9ROR 0.8 · calibrated p 0.198
0.8 EB05 0.8 · IC025 -0.3
PRR-only: not supported by EBGM or IC
vs other alpha-Adrenergic Blockers: only this drug
Reporting / coding artifactage-adj. PRR 0.8 · serious PRR 0.8not reported in cached trials
Acute kidney injury (sudden kidney damage)4,4814.7
4.6–4.8ROR 4.8 · calibrated p 0.254
4.6 EB05 4.5 · IC025 +2.1
3/3 methods agree
vs other alpha-Adrenergic Blockers: PRR 130.2 (110.1–154.1)
Not in label — unassessedage-adj. PRR 2.9 · serious PRR 3.8not reported in cached trials
Fall4,4512.1
2.0–2.2ROR 2.1 · calibrated p 0.981
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
vs other alpha-Adrenergic Blockers: only this drug
Not in label — unassessedage-adj. PRR 1.5 · serious PRR 1.8not reported in cached trials
Pain4,4481.1
1.1–1.2ROR 1.1 · calibrated p 0.395
1.1 EB05 1.1 · IC025 +0.1
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.1NCT00347360: 1/44 (2.3%) control (serious AE)
Headache4,3691.1
1.1–1.1ROR 1.1 · calibrated p 0.367
1.1 EB05 1.1 · IC025 +0.1
vs other alpha-Adrenergic Blockers: only this drug
Labeled adverse reaction
exact term
age-adj. PRR 1.1 · serious PRR 1.1NCT00347360: 1/43 (2.3%) control (serious AE)

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 Carvedilol?

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

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

Do FAERS signals prove that Carvedilol 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.