Carvedilol side effects: what 134,417 FDA adverse event reports show
Drug class
alpha-Adrenergic Blocker, beta-Adrenergic Blocker
Who reports
134,417 reports · 70% serious · 16,351 with death outcome · 47% female
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( .
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.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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). 1,144 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 |
|---|---|---|---|---|---|---|
| Nephrogenic anaemia | 925 | 38.3 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 — unassessed | serious n=925 | not reported in cached trials |
| Hyperparathyroidism secondary | 497 | 38.0 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 — unassessed | serious n=496 · 100% clinician | not reported in cached trials |
| Brash syndrome | 266 | 37.9 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 — unassessed | serious n=266 · 100% clinician | not reported in cached trials |
| Chronic kidney disease-mineral and bone disorder | 210 | 37.7 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 — unassessed | serious n=210 | not reported in cached trials |
| Ischaemic cardiomyopathy | 376 | 21.4 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 increased | 154 | 20.4 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 marker | serious n=152 · 100% clinician | not reported in cached trials |
| Dyspnoea paroxysmal nocturnal | 81 | 19.1 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 — unassessed | serious n=79 · ♀ 0% (drug 47%) | not reported in cached trials |
| Rebound acid hypersecretion | 307 | 17.3 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 — unassessed | serious n=307 | not reported in cached trials |
| Implantable defibrillator insertion | 128 | 16.7 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 — unassessed | serious n=125 · 100% consumer | not reported in cached trials |
| End stage renal disease | 1,755 | 16.3 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 — unassessed | serious PRR 12.2 | not reported in cached trials |
| Left atrial dilatation | 115 | 15.3 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 — unassessed | serious n=115 · 100% clinician | not reported in cached trials |
| Orthopnoea | 271 | 14.4 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 — unassessed | serious n=263 | not reported in cached trials |
| Haemorrhagic anaemia | 355 | 13.4 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 — unassessed | serious n=355 | not reported in cached trials |
| Cardiac failure chronic | 338 | 13.4 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 | Labeled (related wording) related wording | serious n=338 | NCT00347360: 1/44 (2.3%) control (serious AE) |
| Carotid arteriosclerosis | 77 | 12.6 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 — unassessed | serious n=77 · ♀ 0% (drug 47%) · 100% clinician | not reported in cached trials |
| N-terminal prohormone brain natriuretic peptide increased | 103 | 12.3 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 marker | serious n=98 · ♀ 0% (drug 47%) · 100% clinician | not reported in cached trials |
| Product monitoring error | 99 | 11.5 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 artifact | serious n=99 · ♀ 0% (drug 47%) · 100% clinician | not reported in cached trials |
| Echocardiogram abnormal | 93 | 11.1 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 marker | serious n=87 · ♀ 0% (drug 47%) · 100% consumer | not reported in cached trials |
| Renal artery stenosis | 92 | 11.0 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 — unassessed | serious n=92 · 100% clinician | not reported in cached trials |
| Left ventricular hypertrophy | 281 | 10.9 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=277 | not reported in cached trials |
| Ventricular hypokinesia | 211 | 10.9 9.5–12.5ROR 10.9 · calibrated p 0.025 ✓ | 10.1 EB05 9.0 · IC025 +3.1 3/3 methods agree vs other alpha-Adrenergic Blockers: only this drug | Labeled (related wording) related wording | serious n=211 | not reported in cached trials |
| Congestive cardiomyopathy | 277 | 10.9 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=275 | not reported in cached trials |
| Diastolic dysfunction | 202 | 10.8 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=197 | not reported in cached trials |
| Ejection fraction decreased | 952 | 10.1 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 7.9 | not reported in cached trials |
| Bundle branch block left | 260 | 10.1 8.9–11.4ROR 10.1 · calibrated p 0.032 ✓ | 9.4 EB05 8.5 · IC025 +3.0 3/3 methods agree vs other alpha-Adrenergic Blockers: only this drug | Labeled (related wording) related wording | serious n=253 | NCT00347360: 1/44 (2.3%) control (serious AE) |
| Mitral valve incompetence | 671 | 9.8 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 — unassessed | age-adj. PRR 8.0 · serious PRR 7.7 | not reported in cached trials |
| Essential hypertension | 149 | 9.5 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=143 | not reported in cached trials |
| Cardiac failure congestive | 4,455 | 9.0 8.7–9.3ROR 9.3 · calibrated p 0.041 ✓ | 8.6 EB05 8.4 · IC025 +3.0 3/3 methods agree vs other alpha-Adrenergic Blockers: PRR 285.6 (222.8–366.1) | Labeled (related wording) related wording | age-adj. PRR 7.5 · serious PRR 7.1 | NCT00347360: 1/44 (2.3%) control (serious AE) |
| Aortic valve incompetence | 233 | 9.0 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 — unassessed | serious n=234 | not reported in cached trials |
| Chronic kidney disease | 4,057 | 8.7 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 — unassessed | age-adj. PRR 7.8 · serious PRR 6.9 | not reported in cached trials |
| Cardiomyopathy | 782 | 8.7 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 6.8 | not reported in cached trials |
| Tricuspid valve incompetence | 407 | 8.4 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 — unassessed | serious PRR 6.6 | not reported in cached trials |
| Left ventricular dysfunction | 337 | 8.3 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=331 | not reported in cached trials |
| Dilatation ventricular | 107 | 8.2 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=107 | not reported in cached trials |
| Brain natriuretic peptide increased | 154 | 8.2 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 marker | serious n=143 | not reported in cached trials |
| Cardiomegaly | 614 | 8.1 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 6.5 | not reported in cached trials |
| Therapeutic agent toxicity | 166 | 8.0 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 — unassessed | serious n=165 | not reported in cached trials |
| Mitral valve disease | 87 | 8.0 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 — unassessed | serious n=86 · ♀ 0% (drug 47%) · 100% clinician | not reported in cached trials |
| Aortic arteriosclerosis | 122 | 7.7 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 — unassessed | serious n=120 | not reported in cached trials |
| Renal failure chronic | 356 | 7.4 6.7–8.2ROR 7.4 · calibrated p 0.084 | 7.1 EB05 6.5 · IC025 +2.6 3/3 methods agree vs other alpha-Adrenergic Blockers: only this drug | Labeled (related wording) related wording | serious PRR 5.9 | not 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Heart failure | 7,968 | 7.27.1–7.4 | signal |
| Kidney injury | 10,955 | 3.83.7–3.9 | signal |
| Gi bleeding | 4,209 | 3.73.5–3.8 | signal |
| Myocardial infarction | 4,632 | 3.63.5–3.7 | signal |
| Arrhythmia / qt | 4,168 | 3.43.3–3.5 | signal |
| Hypoglycaemia | 1,549 | 2.52.4–2.7 | signal |
| Anaemia | 4,776 | 2.52.4–2.6 | signal |
| Hyponatraemia | 1,169 | 2.32.2–2.4 | signal |
| Stroke | 3,225 | 2.02.0–2.1 | raised |
| Fall / fracture | 4,711 | 1.91.9–2.0 | raised |
| Hyperglycaemia / diabetes | 4,184 | 1.91.8–2.0 | raised |
| Serious infection | 8,459 | 1.71.7–1.8 | raised |
| Thrombocytopenia | 2,169 | 1.51.5–1.6 | raised |
| Rhabdomyolysis / myopathy | 797 | 1.51.4–1.6 | raised |
| Venous thromboembolism | 1,890 | 1.41.3–1.4 | raised |
| Pancreatitis | 650 | 1.31.2–1.4 | raised |
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).
- NCT00347360 — The COREG And Lisinopril Combination Therapy In Hypertensive Subjects (COSMOS) Trial (N=654, PHASE3; 38 AE terms posted; arms: Lisinopril 10; Lisinopril 20; Lisinopril 40; Carvedilol Controlled Release 20)
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Fatigue (tiredness) | 8,913 | 1.8 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 1.7 | NCT00347360: 2/42 (4.8%) on Carvedilol; 1/43 (2.3%) control |
| Dyspnoea (shortness of breath) | 8,393 | 2.3 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 2.1 | NCT00347360: 1/42 (2.4%) on Carvedilol; 1/44 (2.3%) control |
| Diarrhoea (diarrhea) | 7,144 | 1.7 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 1.5 | NCT00347360: 1/42 (2.4%) on Carvedilol; 1/43 (2.3%) control |
| Dizziness | 6,968 | 2.2 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 2.0 | NCT00347360: 4/44 (9.1%) on Carvedilol; 3/43 (7.0%) control |
| Nausea | 6,708 | 1.3 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 1.4 | NCT00347360: 1/42 (2.4%) on Carvedilol (serious AE) |
| Drug ineffective (drug did not work) | 5,836 | 0.7 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 artifact | age-adj. PRR 0.8 · serious PRR 0.8 | not reported in cached trials |
| Death | 5,805 | 1.1 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 reaction | age-adj. PRR 0.9 · serious PRR 0.9 | not reported in cached trials |
| Hypotension (low blood pressure) | 5,698 | 4.5 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 3.5 | not reported in cached trials |
| Asthenia (weakness) | 5,466 | 2.3 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 2.0 | not reported in cached trials |
| Off label use (used outside approved label) | 4,626 | 0.8 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 artifact | age-adj. PRR 0.8 · serious PRR 0.8 | not reported in cached trials |
| Acute kidney injury (sudden kidney damage) | 4,481 | 4.7 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 — unassessed | age-adj. PRR 2.9 · serious PRR 3.8 | not reported in cached trials |
| Cardiac failure congestive | 4,455 | 9.0 8.7–9.3ROR 9.3 · calibrated p 0.041 ✓ | 8.6 EB05 8.4 · IC025 +3.0 3/3 methods agree vs other alpha-Adrenergic Blockers: PRR 285.6 (222.8–366.1) | Labeled (related wording) related wording | age-adj. PRR 7.5 · serious PRR 7.1 | NCT00347360: 1/44 (2.3%) control (serious AE) |
| Fall | 4,451 | 2.1 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 — unassessed | age-adj. PRR 1.5 · serious PRR 1.8 | not reported in cached trials |
| Pain | 4,448 | 1.1 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 1.1 | NCT00347360: 1/44 (2.3%) control (serious AE) |
| Headache | 4,369 | 1.1 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 1.1 | NCT00347360: 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.
- Nephrogenic anaemia — n=925, PRR 38.3
- Hyperparathyroidism secondary — n=497, PRR 38.0
- Brash syndrome — n=266, PRR 37.9
- Chronic kidney disease-mineral and bone disorder — n=210, PRR 37.7
- Dyspnoea paroxysmal nocturnal — n=81, PRR 19.1
- Rebound acid hypersecretion — n=307, PRR 17.3
- Implantable defibrillator insertion — n=128, PRR 16.7
- End stage renal disease — n=1,755, PRR 16.3
- Left atrial dilatation — n=115, PRR 15.3
- Orthopnoea — n=271, PRR 14.4
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
- FDA label via openFDA (set ID 010290af-81f4-0037-e063-6394a90a4638, effective 20260511; matched on
openfda.generic_name.exact:"CARVEDILOL" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 2585 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, 1,184 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
CARVEDILOL, 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.