Valsartan Oral side effects: what 53,986 FDA adverse event reports show
Drug class
Angiotensin 2 Receptor Blocker
Who reports
53,986 reports · 78% serious · 4,309 with death outcome · 56% female
Used for
Valsartan tablets are an angiotensin II receptor blocker (ARB) indicated for: • Hypertension , to lower blood pressure in adults and children 1 year and older. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primar.
What it is
Valsartan is a nonpeptide, orally active, and specific angiotensin II receptor blocker acting on the AT 1 receptor subtype. Valsartan is chemically described as L-valine, N -(1-oxopentyl)- N -[[2′-(1 H -tetrazol-5-yl) [1,1′-biphenyl]-4-yl]methyl]-.
Boxed warning
FETAL TOXICITY WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue valsartan tablets as soon as possible. (5.1) • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. (5.1) WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- 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). 1,164 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 |
|---|---|---|---|---|---|---|
| Femoral hernia incarcerated | 46 | 676.1 418.0–1,093.6ROR 676.7 · calibrated p 6e-14 ✓ | 222.3 EB05 173.4 · IC025 +5.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=46 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Lymphatic fistula | 45 | 318.5 214.4–473.0ROR 318.7 · calibrated p 3e-11 ✓ | 162.3 EB05 126.2 · IC025 +5.4 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=45 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Vaginal flatulence | 124 | 266.2 211.7–334.8ROR 266.8 · calibrated p 5e-11 ✓ | 153.6 EB05 132.3 · IC025 +6.3 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.7 (7.5–12.4) | Not in label — unassessed | serious n=124 · ♀ 100% (drug 56%) | not reported in cached trials |
| Bronchial neoplasm | 50 | 224.8 158.5–318.8ROR 225.0 · calibrated p 4e-10 ✓ | 134.7 EB05 106.2 · IC025 +5.4 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=50 · ♀ 100% (drug 56%) | NCT00097786: 1/2,283 (0.0%) control (serious AE) |
| Merycism | 55 | 95.1 70.8–127.8ROR 95.2 · calibrated p 3e-7 ✓ | 74.5 EB05 59.4 · IC025 +5.1 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=54 · 100% consumer | not reported in cached trials |
| Product impurity | 51 | 87.8 64.8–119.0ROR 87.9 · calibrated p 5e-7 ✓ | 69.8 EB05 55.1 · IC025 +4.9 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Reporting / coding artifact | serious n=51 · 100% consumer | not reported in cached trials |
| Pancreatic steatosis | 47 | 83.2 60.7–114.0ROR 83.2 · calibrated p 8e-7 ✓ | 66.7 EB05 52.2 · IC025 +4.8 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=47 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Bronchial haemorrhage | 52 | 76.7 57.0–103.3ROR 76.8 · calibrated p 1e-6 ✓ | 62.7 EB05 49.6 · IC025 +4.9 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=52 · ♀ 100% (drug 56%) | not reported in cached trials |
| Congenital renal disorder | 41 | 69.6 49.9–97.1ROR 69.7 · calibrated p 3e-6 ✓ | 57.6 EB05 44.2 · IC025 +4.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=41 · 100% clinician | not reported in cached trials |
| Wound infection pseudomonas | 45 | 65.4 47.7–89.7ROR 65.4 · calibrated p 4e-6 ✓ | 54.8 EB05 42.6 · IC025 +4.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=45 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Nasal turbinate hypertrophy | 52 | 62.3 46.5–83.5ROR 62.4 · calibrated p 5e-6 ✓ | 52.7 EB05 41.8 · IC025 +4.7 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Likely indication confounding shares a disease stem with the indications wording | serious n=52 · ♀ 100% (drug 56%) | NCT00097786: 1/2,316 (0.0%) control (serious AE) |
| Endometrial ablation | 49 | 62.2 46.0–84.1ROR 62.3 · calibrated p 5e-6 ✓ | 52.6 EB05 41.4 · IC025 +4.7 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=49 · ♀ 100% (drug 56%) | not reported in cached trials |
| Tissue infiltration | 40 | 61.4 44.0–85.7ROR 61.4 · calibrated p 6e-6 ✓ | 51.8 EB05 39.7 · IC025 +4.5 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=40 · ♀ 100% (drug 56%) · 100% consumer | not reported in cached trials |
| Physical deconditioning | 264 | 45.7 40.2–51.9ROR 45.9 · calibrated p 2e-5 ✓ | 40.8 EB05 36.8 · IC025 +5.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 8.1 (6.8–9.5) | Not in label — unassessed | serious n=264 | not reported in cached trials |
| Foetal disorder | 86 | 43.9 35.2–54.9ROR 44.0 · calibrated p 4e-5 ✓ | 39.2 EB05 32.7 · IC025 +4.7 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.6 (7.1–12.9) | Labeled (related wording) related wording | serious n=85 · 100% clinician | not reported in cached trials |
| Multiple drug therapy | 55 | 33.2 25.2–43.7ROR 33.2 · calibrated p 2e-4 ✓ | 30.3 EB05 24.2 · IC025 +4.1 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 35.5 (20.0–62.7) | Reporting / coding artifact | serious n=55 · ♀ 100% (drug 56%) · 100% clinician | NCT00097786: 1/2,297 (0.0%) on Valsartan Oral (serious AE) |
| Female genital tract fistula | 135 | 33.0 27.7–39.3ROR 33.1 · calibrated p 2e-4 ✓ | 30.3 EB05 26.3 · IC025 +4.5 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.6 (7.6–12.2) | Not in label — unassessed | serious n=135 · ♀ 100% (drug 56%) | NCT00097786: 1/2,297 (0.0%) on Valsartan Oral (serious AE) |
| Fear of disease | 135 | 31.5 26.4–37.5ROR 31.6 · calibrated p 2e-4 ✓ | 29.1 EB05 25.2 · IC025 +4.4 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.1 (7.2–11.5) | Not in label — unassessed | serious n=134 | not reported in cached trials |
| Oligohydramnios | 251 | 31.4 27.6–35.7ROR 31.5 · calibrated p 2e-4 ✓ | 29.0 EB05 26.1 · IC025 +4.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 8.5 (7.2–10.0) | Labeled — boxed warning exact term | serious n=249 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Pulmonary hypoplasia | 58 | 30.5 23.3–39.8ROR 30.5 · calibrated p 3e-4 ✓ | 28.1 EB05 22.5 · IC025 +4.1 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=58 · 100% clinician | not reported in cached trials |
| Multi-organ disorder | 137 | 28.7 24.1–34.2ROR 28.8 · calibrated p 4e-4 ✓ | 26.7 EB05 23.1 · IC025 +4.3 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.2 (7.3–11.6) | Not in label — unassessed | serious n=136 · ♀ 100% (drug 56%) | NCT00097786: 2/2,305 (0.1%) on Valsartan Oral; 4/2,283 (0.2%) control (serious AE) |
| Macular degeneration | 815 | 28.5 26.5–30.5ROR 28.9 · calibrated p 3e-4 ✓ | 26.5 EB05 25.0 · IC025 +4.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 7.4 (6.7–8.1) | Not in label — unassessed | serious PRR 21.0 · ♀ 100% (drug 56%) | NCT00097786: 1/2,316 (0.0%) on Valsartan Oral; 1/2,305 (0.0%) control (serious AE) |
| Osteochondrosis | 79 | 28.1 22.3–35.3ROR 28.1 · calibrated p 4e-4 ✓ | 26.1 EB05 21.6 · IC025 +4.1 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.5 (7.0–13.0) | Not in label — unassessed | serious n=79 · ♀ 36% (drug 56%) | NCT00097786: 1/2,305 (0.0%) on Valsartan Oral; 3/2,283 (0.1%) control (serious AE) |
| Orthostatic intolerance | 39 | 22.4 16.2–31.0ROR 22.4 · calibrated p 0.002 ✓ | 21.0 EB05 16.0 · IC025 +3.5 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=39 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Rhonchi | 75 | 22.2 17.6–28.0ROR 22.2 · calibrated p 0.001 ✓ | 20.9 EB05 17.2 · IC025 +3.8 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 8.0 (5.9–10.8) | Not in label — unassessed | serious n=75 · ♀ 100% (drug 56%) | not reported in cached trials |
| Brash syndrome | 73 | 22.0 17.4–27.9ROR 22.1 · calibrated p 0.001 ✓ | 20.8 EB05 17.1 · IC025 +3.8 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 6.1 (4.5–8.2) | Not in label — unassessed | serious n=73 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Carotid arteriosclerosis | 54 | 21.6 16.4–28.4ROR 21.6 · calibrated p 0.002 ✓ | 20.3 EB05 16.2 · IC025 +3.7 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 6.7 (4.7–9.5) | Not in label — unassessed | serious n=54 · ♀ 0% (drug 56%) | NCT00097786: 1/2,305 (0.0%) on Valsartan Oral; 2/2,283 (0.1%) control (serious AE) |
| Adenoma benign | 45 | 21.3 15.8–28.8ROR 21.3 · calibrated p 0.002 ✓ | 20.1 EB05 15.6 · IC025 +3.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=45 · ♀ 100% (drug 56%) · 100% consumer | not reported in cached trials |
| Radiculopathy | 137 | 21.2 17.9–25.2ROR 21.3 · calibrated p 0.002 ✓ | 20.1 EB05 17.4 · IC025 +4.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 7.2 (5.7–8.9) | Not in label — unassessed | serious n=137 · ♀ 100% (drug 56%) | NCT00097786: 1/2,305 (0.0%) on Valsartan Oral; 2/2,283 (0.1%) control (serious AE) |
| Chronic sinusitis | 192 | 20.9 18.1–24.2ROR 21.0 · calibrated p 0.002 ✓ | 19.9 EB05 17.6 · IC025 +4.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 6.6 (5.5–8.0) | Not in label — unassessed | serious n=189 · ♀ 100% (drug 56%) | NCT00097786: 1/2,297 (0.0%) on Valsartan Oral (serious AE) |
| Hypochromic anaemia | 50 | 20.1 15.1–26.7ROR 20.1 · calibrated p 0.002 ✓ | 19.0 EB05 15.0 · IC025 +3.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=50 · ♀ 100% (drug 56%) | NCT00097786: 1/2,283 (0.0%) control (serious AE) |
| Proctitis | 131 | 19.0 15.9–22.6ROR 19.0 · calibrated p 0.003 ✓ | 18.1 EB05 15.6 · IC025 +3.8 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.2 (7.2–11.7) | Not in label — unassessed | serious n=131 · ♀ 100% (drug 56%) | not reported in cached trials |
| Arterial haemorrhage | 53 | 18.7 14.2–24.7ROR 18.8 · calibrated p 0.003 ✓ | 17.8 EB05 14.1 · IC025 +3.5 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=53 · ♀ 100% (drug 56%) · 100% clinician | NCT00097786: 1/2,283 (0.0%) control (serious AE) |
| Obstructive sleep apnoea syndrome | 59 | 17.1 13.2–22.2ROR 17.1 · calibrated p 0.005 ✓ | 16.3 EB05 13.1 · IC025 +3.4 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=58 · 100% consumer | not reported in cached trials |
| Lymphocyte count abnormal | 45 | 16.1 11.9–21.7ROR 16.1 · calibrated p 0.006 ✓ | 15.3 EB05 11.8 · IC025 +3.2 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Lab value / disease marker | serious n=45 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Seroma | 50 | 15.8 11.9–21.0ROR 15.8 · calibrated p 0.006 ✓ | 15.1 EB05 11.8 · IC025 +3.3 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=50 · ♀ 100% (drug 56%) · 100% clinician | NCT00097786: 1/2,305 (0.0%) on Valsartan Oral; 1/2,283 (0.0%) control (serious AE) |
| Blood pressure inadequately controlled | 232 | 15.4 13.5–17.6ROR 15.5 · calibrated p 0.006 ✓ | 14.8 EB05 13.3 · IC025 +3.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 2.2 (1.9–2.5) | Labeled (related wording) related wording | serious n=194 | not reported in cached trials |
| Renal neoplasm | 80 | 15.1 12.1–18.9ROR 15.1 · calibrated p 0.007 ✓ | 14.5 EB05 12.0 · IC025 +3.4 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 7.4 (5.5–9.9) | Not in label — unassessed | serious n=79 · ♀ 100% (drug 56%) | NCT00097786: 1/2,297 (0.0%) on Valsartan Oral; 1/2,283 (0.0%) control (serious AE) |
| Major depression | 267 | 14.7 13.0–16.6ROR 14.7 · calibrated p 0.008 ✓ | 14.1 EB05 12.8 · IC025 +3.6 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 9.0 (7.6–10.6) | Not in label — unassessed | serious PRR 10.9 | NCT00097786: 1/2,305 (0.0%) on Valsartan Oral; 4/2,283 (0.2%) control (serious AE) |
| Aortic dilatation | 39 | 14.4 10.4–19.8ROR 14.4 · calibrated p 0.010 ✓ | 13.6 EB05 10.2 · IC025 +3.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: only this drug | Not in label — unassessed | serious n=39 · ♀ 0% (drug 56%) · 100% consumer | NCT00097786: 1/2,297 (0.0%) on Valsartan Oral (serious AE) |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Valsartan Oral 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 (16 of 40 signal terms matched).
- NCT00097786 — Long-term Study of Nateglinide+Valsartan to Prevent or Delay Type II Diabetes Mellitus and Cardiovascular Comp (N=9306, PHASE3; 1704 AE terms posted; arms: Valsartan 160 mg od + Nateglinide 60 mg ; Valsartan 160 mg od + Placebo Nateglinid; Nateglinide 60 mg ac + Placebo Valsartan; Placebo)
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 |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 3,870 | 1.1 1.1–1.2ROR 1.2 · calibrated p 0.408 | 1.1 EB05 1.1 · IC025 +0.1 vs other Angiotensin 2 Receptor Blockers: PRR 3.0 (2.9–3.1) | Reporting / coding artifact | serious PRR 1.6 | not reported in cached trials |
| Fatigue (tiredness) | 3,089 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.693 | 1.5 EB05 1.5 · IC025 +0.6 vs other Angiotensin 2 Receptor Blockers: PRR 1.6 (1.6–1.7) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT00097786: 1/2,305 (0.0%) control (serious AE) |
| Dyspnoea (shortness of breath) | 2,908 | 2.0 1.9–2.1ROR 2.1 · calibrated p 0.976 | 2.0 EB05 1.9 · IC025 +0.9 vs other Angiotensin 2 Receptor Blockers: PRR 1.6 (1.5–1.7) | Not in label — unassessed | serious PRR 1.8 | NCT00097786: 28/2,305 (1.2%) on Valsartan Oral; 15/2,283 (0.7%) control (serious AE) |
| Nausea | 2,844 | 1.4 1.4–1.5ROR 1.4 · calibrated p 0.591 | 1.4 EB05 1.4 · IC025 +0.4 vs other Angiotensin 2 Receptor Blockers: PRR 2.5 (2.4–2.6) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT00097786: 9/2,305 (0.4%) on Valsartan Oral; 10/2,283 (0.4%) control (serious AE) |
| Diarrhoea (diarrhea) | 2,768 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.776 | 1.7 EB05 1.6 · IC025 +0.7 vs other Angiotensin 2 Receptor Blockers: PRR 2.5 (2.4–2.6) | Labeled adverse reaction exact term | serious PRR 1.6 | NCT00097786: 9/2,305 (0.4%) on Valsartan Oral; 7/2,283 (0.3%) control (serious AE) |
| Dizziness | 2,750 | 2.2 2.1–2.2ROR 2.2 · calibrated p 0.945 | 2.1 EB05 2.1 · IC025 +1.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 1.6 (1.5–1.6) | Labeled adverse reaction exact term | serious PRR 2.1 | NCT00097786: 13/2,305 (0.6%) on Valsartan Oral; 10/2,283 (0.4%) control (serious AE) |
| Headache | 2,448 | 1.5 1.5–1.6ROR 1.5 · calibrated p 0.671 | 1.5 EB05 1.5 · IC025 +0.5 vs other Angiotensin 2 Receptor Blockers: PRR 2.5 (2.4–2.6) | Labeled adverse reaction exact term | serious PRR 1.7 | NCT00097786: 1/2,305 (0.0%) control (serious AE) |
| Acute kidney injury (sudden kidney damage) | 2,389 | 6.2 5.9–6.4ROR 6.4 · calibrated p 0.126 | 6.1 EB05 5.9 · IC025 +2.5 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 3.0 (2.9–3.1) | Labeled — boxed warning synonym match | serious PRR 4.5 | not reported in cached trials |
| Off label use (used outside approved label) | 2,174 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.288 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC vs other Angiotensin 2 Receptor Blockers: PRR 2.8 (2.7–2.9) | Reporting / coding artifact | serious PRR 1.0 | not reported in cached trials |
| Hypertension (high blood pressure) | 2,024 | 3.7 3.6–3.9ROR 3.8 · calibrated p 0.409 | 3.7 EB05 3.6 · IC025 +1.8 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 2.2 (2.1–2.3) | Labeled — boxed warning exact term | serious PRR 3.0 | NCT00097786: 4/2,305 (0.2%) on Valsartan Oral; 2/2,283 (0.1%) control (serious AE) |
| Asthenia (weakness) | 1,969 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.986 | 2.0 EB05 2.0 · IC025 +0.9 vs other Angiotensin 2 Receptor Blockers: PRR 1.9 (1.8–2.0) | Not in label — unassessed | serious PRR 1.8 | NCT00097786: 6/2,305 (0.3%) on Valsartan Oral; 6/2,283 (0.3%) control (serious AE) |
| Pain | 1,881 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.436 | 1.2 EB05 1.1 · IC025 +0.2 vs other Angiotensin 2 Receptor Blockers: PRR 2.3 (2.1–2.4) | Labeled adverse reaction exact term | serious PRR 1.1 | NCT00097786: 15/2,305 (0.7%) on Valsartan Oral; 13/2,283 (0.6%) control (serious AE) |
| Fall | 1,793 | 2.1 2.0–2.2ROR 2.1 · calibrated p 0.983 | 2.1 EB05 2.0 · IC025 +1.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 1.8 (1.7–1.9) | Not in label — unassessed | serious PRR 1.7 | NCT00097786: 59/2,305 (2.6%) on Valsartan Oral; 47/2,283 (2.1%) control (serious AE) |
| Malaise (feeling unwell) | 1,742 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.680 | 1.5 EB05 1.5 · IC025 +0.5 vs other Angiotensin 2 Receptor Blockers: PRR 1.6 (1.5–1.6) | Not in label — unassessed | serious PRR 1.5 | NCT00097786: 2/2,297 (0.1%) on Valsartan Oral; 1/2,316 (0.0%) control (serious AE) |
| Blood pressure increased | 1,721 | 4.4 4.2–4.6ROR 4.5 · calibrated p 0.295 | 4.4 EB05 4.2 · IC025 +2.0 3/3 methods agree vs other Angiotensin 2 Receptor Blockers: PRR 2.0 (1.9–2.1) | Labeled — boxed warning synonym match | serious PRR 3.6 | NCT00097786: 2/2,305 (0.1%) 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.
- Femoral hernia incarcerated — n=46, PRR 676.1
- Lymphatic fistula — n=45, PRR 318.5
- Vaginal flatulence — n=124, PRR 266.2
- Bronchial neoplasm — n=50, PRR 224.8 (also seen in trial arm)
- Merycism — n=55, PRR 95.1
- Pancreatic steatosis — n=47, PRR 83.2
- Bronchial haemorrhage — n=52, PRR 76.7
- Congenital renal disorder — n=41, PRR 69.6
- Wound infection pseudomonas — n=45, PRR 65.4
- Endometrial ablation — n=49, PRR 62.2
✓ A hand-written Bradford Hill causality assessment exists for this drug: Valsartan ↔ Acute kidney injury.
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 Valsartan Oral?
In FDA FAERS, the most frequently co-reported reaction terms for Valsartan Oral are fatigue, dyspnoea, nausea, diarrhoea, dizziness, headache. 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 Valsartan Oral have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: FETAL TOXICITY WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue valsartan tablets as soon as possible. (5.1) • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. (5.1) WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning.
Do FAERS signals prove that Valsartan Oral 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 0878f27e-5368-c93f-e063-6394a90a1086, effective 20250109; matched on
openfda.generic_name.exact:"VALSARTAN") - 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, 1,204 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
VALSARTAN, 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.