Ondansetron Hydrochloride side effects: what 121,725 FDA adverse event reports show
Drug class
Serotonin-3 Receptor Antagonist
Who reports
121,725 reports · 79% serious · 15,159 with death outcome · 62% female
Used for
Ondansetron orally disintegrating tablets are indicated for the prevention of nausea and vomiting associated with: highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m 2 initial and repeat courses of moderately em.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- 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). 1,163 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 |
|---|---|---|---|---|---|---|
| Appendicolith | 287 | 550.6 433.7–699.1ROR 551.9 · calibrated p 4e-14 ✓ | 128.9 EB05 116.8 · IC025 +6.5 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (2.0–2.7) | Not in label — unassessed | serious n=287 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Sleep disorder therapy | 137 | 492.1 353.4–685.4ROR 492.7 · calibrated p 3e-13 ✓ | 124.3 EB05 107.8 · IC025 +6.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.7 (2.2–3.4) | Reporting / coding artifact | serious n=137 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Antacid therapy | 83 | 389.3 263.3–575.6ROR 389.5 · calibrated p 4e-12 ✓ | 115.4 EB05 96.0 · IC025 +5.8 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.8 (2.1–3.7) | Reporting / coding artifact | serious n=83 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Lymphoid tissue hypoplasia | 84 | 225.1 162.4–312.1ROR 225.3 · calibrated p 4e-10 ✓ | 95.0 EB05 79.1 · IC025 +5.6 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: only this drug | Not in label — unassessed | serious n=84 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Thymus hypoplasia | 82 | 157.3 116.5–212.5ROR 157.4 · calibrated p 7e-9 ✓ | 80.4 EB05 66.9 · IC025 +5.4 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: only this drug | Not in label — unassessed | serious n=82 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Analgesic therapy | 137 | 139.3 111.1–174.7ROR 139.5 · calibrated p 1e-8 ✓ | 76.0 EB05 65.9 · IC025 +5.6 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.7 (2.2–3.3) | Reporting / coding artifact | serious n=137 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Drug therapy | 123 | 107.6 85.8–134.9ROR 107.7 · calibrated p 9e-8 ✓ | 65.5 EB05 56.3 · IC025 +5.4 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.7 (2.2–3.4) | Reporting / coding artifact | serious n=123 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Left-to-right cardiac shunt | 93 | 78.5 61.4–100.4ROR 78.6 · calibrated p 9e-7 ✓ | 53.4 EB05 44.9 · IC025 +5.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 3.0 (2.3–3.9) | Not in label — unassessed | serious n=93 · 100% consumer | no trial arm names this drug |
| Anticoagulant therapy | 86 | 77.2 59.8–99.7ROR 77.3 · calibrated p 1e-6 ✓ | 52.7 EB05 44.0 · IC025 +5.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.8 (2.1–3.7) | Reporting / coding artifact | serious n=86 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Neurologic neglect syndrome | 170 | 74.9 62.6–89.8ROR 75.0 · calibrated p 1e-6 ✓ | 51.9 EB05 45.7 · IC025 +5.3 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.9 (2.4–3.5) | Not in label — unassessed | serious n=170 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Carotid artery thrombosis | 180 | 45.8 38.9–54.0ROR 45.9 · calibrated p 3e-5 ✓ | 36.1 EB05 31.9 · IC025 +4.8 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.8 (2.4–3.4) | Not in label — unassessed | serious n=180 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Disseminated aspergillosis | 88 | 39.6 31.4–50.0ROR 39.6 · calibrated p 7e-5 ✓ | 32.1 EB05 26.8 · IC025 +4.4 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: only this drug | Not in label — unassessed | serious n=88 · ♀ 0% (drug 62%) | no trial arm names this drug |
| Adjustment disorder | 176 | 26.7 22.8–31.3ROR 26.8 · calibrated p 5e-4 ✓ | 23.2 EB05 20.4 · IC025 +4.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.8 (2.3–3.4) | Not in label — unassessed | serious n=175 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 142 | 26.1 21.8–31.1ROR 26.1 · calibrated p 6e-4 ✓ | 22.6 EB05 19.7 · IC025 +4.1 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (1.8–2.7) | Not in label — unassessed | serious n=142 | no trial arm names this drug |
| Temperature regulation disorder | 287 | 25.9 22.9–29.3ROR 26.0 · calibrated p 6e-4 ✓ | 22.6 EB05 20.5 · IC025 +4.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.6 (2.2–3.0) | Not in label — unassessed | serious n=282 · ♀ 100% (drug 62%) | no trial arm names this drug |
| Aplastic anaemia | 539 | 19.6 18.0–21.5ROR 19.7 · calibrated p 0.002 ✓ | 17.7 EB05 16.5 · IC025 +4.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.1 (1.9–2.3) | Not in label — unassessed | serious n=539 · 95% clinician | no trial arm names this drug |
| Hyperphosphataemia | 217 | 19.5 17.0–22.5ROR 19.6 · calibrated p 0.002 ✓ | 17.6 EB05 15.7 · IC025 +3.9 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.5 (2.1–2.9) | Not in label — unassessed | serious n=216 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Nephrogenic anaemia | 470 | 19.1 17.4–21.1ROR 19.2 · calibrated p 0.002 ✓ | 17.3 EB05 16.0 · IC025 +3.9 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.0–2.5) | Not in label — unassessed | serious n=470 | no trial arm names this drug |
| Blood phosphorus increased | 251 | 17.4 15.3–19.8ROR 17.4 · calibrated p 0.004 ✓ | 15.8 EB05 14.2 · IC025 +3.7 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (2.1–2.8) | Lab value / disease marker | serious n=243 · ♀ 0% (drug 62%) · 91% clinician | no trial arm names this drug |
| Hyperparathyroidism secondary | 229 | 17.0 14.9–19.5ROR 17.1 · calibrated p 0.004 ✓ | 15.5 EB05 13.9 · IC025 +3.7 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (1.9–2.7) | Not in label — unassessed | serious n=229 | no trial arm names this drug |
| Febrile neutropenia | 4,861 | 13.6 13.2–14.0ROR 14.1 · calibrated p 0.009 ✓ | 12.6 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 1.9 (1.9–2.0) | Not in label — unassessed | age-adj. PRR 12.7 · serious PRR 9.2 · 94% clinician | no trial arm names this drug |
| Rebound acid hypersecretion | 215 | 12.9 11.2–14.8ROR 12.9 · calibrated p 0.013 ✓ | 12.0 EB05 10.7 · IC025 +3.3 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (1.9–2.6) | Not in label — unassessed | serious n=215 | no trial arm names this drug |
| Infusion site discharge | 115 | 12.3 10.2–14.9ROR 12.4 · calibrated p 0.016 ✓ | 11.5 EB05 9.8 · IC025 +3.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: only this drug | Not in label — unassessed | ♀ 100% (drug 62%) · 100% consumer | no trial arm names this drug |
| Personality disorder | 176 | 12.2 10.5–14.3ROR 12.3 · calibrated p 0.016 ✓ | 11.4 EB05 10.0 · IC025 +3.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.8 (2.4–3.4) | Not in label — unassessed | serious n=176 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Foetal death | 335 | 11.8 10.6–13.2ROR 11.9 · calibrated p 0.018 ✓ | 11.1 EB05 10.1 · IC025 +3.3 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.5 (2.2–2.9) | Not in label — unassessed | serious n=335 · ♀ 100% (drug 62%) | no trial arm names this drug |
| Platelet transfusion | 82 | 11.7 9.4–14.7ROR 11.7 · calibrated p 0.020 ✓ | 10.9 EB05 9.0 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (1.8–3.0) | Not in label — unassessed | serious n=82 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Neutropenic sepsis | 441 | 11.2 10.2–12.4ROR 11.3 · calibrated p 0.021 ✓ | 10.6 EB05 9.8 · IC025 +3.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.1 (1.8–2.3) | Not in label — unassessed | serious PRR 7.7 · 93% clinician | no trial arm names this drug |
| Food allergy | 465 | 11.2 10.2–12.3ROR 11.3 · calibrated p 0.021 ✓ | 10.6 EB05 9.8 · IC025 +3.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.7 (2.4–3.0) | Not in label — unassessed | serious n=457 · ♀ 100% (drug 62%) | no trial arm names this drug |
| Neutropenic colitis | 123 | 10.9 9.1–13.0ROR 10.9 · calibrated p 0.025 ✓ | 10.1 EB05 8.7 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 1.8 (1.5–2.3) | Not in label — unassessed | serious n=122 · 100% clinician | no trial arm names this drug |
| Torsade de pointes | 465 | 10.8 9.8–11.8ROR 10.8 · calibrated p 0.025 ✓ | 10.1 EB05 9.4 · IC025 +3.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (2.1–2.6) | Labeled adverse reaction exact term | serious PRR 7.4 · 100% clinician | no trial arm names this drug |
| Heart disease congenital | 201 | 10.2 8.9–11.8ROR 10.2 · calibrated p 0.031 ✓ | 9.6 EB05 8.5 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.9 (2.4–3.4) | Labeled (related wording) related wording | serious n=201 | no trial arm names this drug |
| Febrile bone marrow aplasia | 229 | 9.9 8.7–11.3ROR 9.9 · calibrated p 0.034 ✓ | 9.3 EB05 8.3 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (1.9–2.7) | Not in label — unassessed | serious n=229 · 100% clinician | no trial arm names this drug |
| Long qt syndrome | 127 | 9.5 8.0–11.4ROR 9.5 · calibrated p 0.039 ✓ | 8.9 EB05 7.7 · IC025 +2.8 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (1.9–3.0) | Labeled adverse reaction exact term | serious n=127 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Ventricular fibrillation | 581 | 9.4 8.7–10.2ROR 9.5 · calibrated p 0.039 ✓ | 8.9 EB05 8.3 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.1–2.6) | Labeled (related wording) related wording | age-adj. PRR 8.4 · serious PRR 6.5 · ♀ 35% (drug 62%) · 95% clinician | no trial arm names this drug |
| Aplasia | 103 | 9.3 7.6–11.4ROR 9.3 · calibrated p 0.043 ✓ | 8.7 EB05 7.3 · IC025 +2.8 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.1 (1.7–2.7) | Not in label — unassessed | serious n=103 · 100% clinician | no trial arm names this drug |
| Pseudomonal sepsis | 90 | 9.2 7.5–11.4ROR 9.2 · calibrated p 0.045 ✓ | 8.6 EB05 7.1 · IC025 +2.7 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (1.8–3.0) | Not in label — unassessed | serious n=90 · ♀ 0% (drug 62%) · 100% clinician | no trial arm names this drug |
| Serotonin syndrome | 975 | 9.2 8.6–9.8ROR 9.3 · calibrated p 0.042 ✓ | 8.8 EB05 8.3 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (2.0–2.3) | Labeled adverse reaction exact term | age-adj. PRR 8.0 · serious PRR 6.4 · 92% clinician | no trial arm names this drug |
| Oculogyric crisis | 107 | 9.2 7.5–11.1ROR 9.2 · calibrated p 0.045 ✓ | 8.5 EB05 7.2 · IC025 +2.8 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (1.7–2.8) | Labeled adverse reaction exact term | serious n=107 · ♀ 100% (drug 62%) · 100% clinician | no trial arm names this drug |
| Vascular device infection | 229 | 9.1 8.0–10.4ROR 9.2 · calibrated p 0.044 ✓ | 8.6 EB05 7.7 · IC025 +2.9 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.9 (2.4–3.4) | Not in label — unassessed | serious n=228 | no trial arm names this drug |
| End stage renal disease | 928 | 9.1 8.5–9.7ROR 9.1 · calibrated p 0.044 ✓ | 8.6 EB05 8.2 · IC025 +3.0 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.1–2.5) | Not in label — unassessed | serious PRR 6.3 | no 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Neutropenia / agranulocytosis | 8,275 | 5.95.8–6.0 | signal |
| Hyponatraemia | 1,720 | 3.73.6–3.9 | signal |
| Thrombocytopenia | 4,571 | 3.63.5–3.7 | signal |
| Anaemia | 5,057 | 2.92.9–3.0 | signal |
| Arrhythmia / qt | 3,116 | 2.82.7–2.9 | signal |
| Kidney injury | 6,669 | 2.52.5–2.6 | signal |
| Serious infection | 10,717 | 2.42.4–2.5 | signal |
| Anaphylaxis / angioedema | 1,621 | 2.22.1–2.4 | signal |
| Venous thromboembolism | 2,479 | 2.01.9–2.1 | raised |
| Pancreatitis | 908 | 1.91.8–2.1 | raised |
| Liver injury | 3,287 | 1.91.8–2.0 | raised |
| Severe cutaneous reaction | 647 | 1.51.4–1.6 | raised |
| Interstitial lung disease | 811 | 1.51.4–1.6 | raised |
| Extrapyramidal | 867 | 1.41.3–1.5 | raised |
| Gi bleeding | 1,491 | 1.41.3–1.5 | raised |
| Seizure | 1,537 | 1.31.3–1.4 | raised |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Nausea | 14,459 | 3.2 3.1–3.2ROR 3.5 · calibrated p 0.487 | 3.2 EB05 3.1 · IC025 +1.6 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.3–2.4) | Likely indication confounding term in indications; also in warnings | age-adj. PRR 2.8 · serious PRR 3.2 | no trial arm names this drug |
| Fatigue (tiredness) | 10,275 | 2.3 2.3–2.3ROR 2.4 · calibrated p 0.851 | 2.3 EB05 2.2 · IC025 +1.2 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (2.3–2.4) | Labeled adverse reaction exact term | age-adj. PRR 2.0 · serious PRR 2.1 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 9,490 | 2.6 2.5–2.6ROR 2.7 · calibrated p 0.734 | 2.5 EB05 2.5 · IC025 +1.3 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.2–2.3) | Labeled adverse reaction exact term | age-adj. PRR 2.2 · serious PRR 2.4 | no trial arm names this drug |
| Vomiting | 8,779 | 3.3 3.2–3.3ROR 3.4 · calibrated p 0.499 | 3.2 EB05 3.2 · IC025 +1.7 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.2–2.3) | Likely indication confounding term in indications; also in warnings | age-adj. PRR 2.9 · serious PRR 2.9 | no trial arm names this drug |
| Off label use (used outside approved label) | 8,027 | 1.6 1.6–1.6ROR 1.6 · calibrated p 0.731 | 1.6 EB05 1.6 · IC025 +0.6 vs other Serotonin-3 Receptor Antagonists: PRR 2.4 (2.3–2.4) | Reporting / coding artifact | age-adj. PRR 1.5 · serious PRR 1.7 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 5,970 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.870 | 1.8 EB05 1.8 · IC025 +0.8 vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.3–2.4) | Labeled (related wording) related wording | age-adj. PRR 1.6 · serious PRR 1.6 | no trial arm names this drug |
| Headache | 5,638 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.695 | 1.5 EB05 1.5 · IC025 +0.6 vs other Serotonin-3 Receptor Antagonists: PRR 2.6 (2.5–2.7) | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.7 | no trial arm names this drug |
| Death | 5,624 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.393 | 1.1 EB05 1.1 · IC025 +0.1 vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (2.1–2.3) | Outcome field, not a reaction | age-adj. PRR 1.2 · serious PRR 0.8 | no trial arm names this drug |
| Pyrexia (fever) | 5,614 | 2.8 2.7–2.9ROR 2.9 · calibrated p 0.657 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.2 (2.1–2.2) | Labeled adverse reaction exact term | age-adj. PRR 2.4 · serious PRR 2.4 | no trial arm names this drug |
| Pain | 5,528 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.692 | 1.5 EB05 1.5 · IC025 +0.6 vs other Serotonin-3 Receptor Antagonists: PRR 2.5 (2.4–2.6) | Not in label — unassessed | age-adj. PRR 1.5 · serious PRR 1.4 | no trial arm names this drug |
| Febrile neutropenia | 4,861 | 13.6 13.2–14.0ROR 14.1 · calibrated p 0.009 ✓ | 12.6 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 1.9 (1.9–2.0) | Not in label — unassessed | age-adj. PRR 12.7 · serious PRR 9.2 · 94% clinician | no trial arm names this drug |
| Constipation | 4,763 | 3.9 3.7–4.0ROR 4.0 · calibrated p 0.384 | 3.8 EB05 3.7 · IC025 +1.9 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.2–2.4) | Labeled adverse reaction exact term | age-adj. PRR 3.5 · serious PRR 3.8 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 4,569 | 0.6 0.6–0.6ROR 0.6 · calibrated p 0.077 | 0.6 EB05 0.6 · IC025 -0.8 PRR-only: not supported by EBGM or IC vs other Serotonin-3 Receptor Antagonists: PRR 2.5 (2.4–2.6) | Reporting / coding artifact | age-adj. PRR 0.7 · serious PRR 0.9 | no trial arm names this drug |
| Asthenia (weakness) | 4,558 | 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 Serotonin-3 Receptor Antagonists: PRR 2.4 (2.3–2.5) | Not in label — unassessed | age-adj. PRR 1.8 · serious PRR 1.8 | no trial arm names this drug |
| Pneumonia (lung infection) | 4,216 | 2.3 2.2–2.3ROR 2.3 · calibrated p 0.900 | 2.2 EB05 2.2 · IC025 +1.1 3/3 methods agree vs other Serotonin-3 Receptor Antagonists: PRR 2.3 (2.2–2.4) | Not in label — unassessed | age-adj. PRR 2.0 · serious PRR 1.7 | no 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.
- Appendicolith — n=287, PRR 550.6
- Lymphoid tissue hypoplasia — n=84, PRR 225.1
- Thymus hypoplasia — n=82, PRR 157.3
- Left-to-right cardiac shunt — n=93, PRR 78.5
- Neurologic neglect syndrome — n=170, PRR 74.9
- Carotid artery thrombosis — n=180, PRR 45.8
- Disseminated aspergillosis — n=88, PRR 39.6
- Adjustment disorder — n=176, PRR 26.7
- Chronic kidney disease-mineral and bone disorder — n=142, PRR 26.1
- Temperature regulation disorder — n=287, PRR 25.9
✓ A hand-written Bradford Hill causality assessment exists for this drug: Ondansetron (5-HT3 antagonists) ↔ QT prolongation / torsades.
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 Ondansetron?
In FDA FAERS, the most frequently co-reported reaction terms for Ondansetron are nausea, fatigue, diarrhoea, vomiting, dyspnoea, 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 Ondansetron have an FDA boxed warning?
No. The FDA label retrieved for Ondansetron has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Ondansetron 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 10afd68b-877f-4819-a314-39f2d56d5db9, effective 20250915; matched on
openfda.generic_name.exact:"ONDANSETRON" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 4595 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, 1,203 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
ONDANSETRON, 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.