Ipilimumab side effects: what 42,905 FDA adverse event reports show
Drug class
CTLA-4-directed Blocking Antibody
Brand names
Yervoy
Who reports
42,905 reports · 89% serious · 9,586 with death outcome · 36% female
Used for
YERVOY is a human cytotoxic T-lymphocyte antigen 4 (CTLA-4)-blocking antibody indicated for: Melanoma • Treatment of unresectable or metastatic melanoma in adults and pediatric patients 12 years and older as a single agent or in combination with nivolumab.
What it is
Ipilimumab is a human cytotoxic T-lymphocyte antigen 4 (CTLA-4)-blocking antibody. Ipilimumab is a recombinant IgG1 kappa immunoglobulin with an approximate molecular weight of 148 kDa. Ipilimumab is produced in mammalian (Chinese hamster ovary) cell culture.
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.
- 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). 1,091 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 |
|---|---|---|---|---|---|---|
| Hypophysitis | 1,074 | 566.7 519.1–618.7ROR 581.2 · calibrated p 1e-14 ✓ | 259.6 EB05 246.8 · IC025 +7.8 3/3 methods agree | Labeled adverse reaction exact term | serious n=922 | NCT02477826: 2/126 (1.6%) on Ipilimumab (serious AE) |
| Lymphocytic hypophysitis | 142 | 521.6 411.4–661.3ROR 523.3 · calibrated p 7e-14 ✓ | 242.6 EB05 211.0 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=139 · 96% clinician | not reported in cached trials |
| Autoimmune colitis | 283 | 386.9 330.9–452.3ROR 389.4 · calibrated p 1e-12 ✓ | 211.8 EB05 191.9 · IC025 +7.1 3/3 methods agree | Labeled (related wording) related wording | serious n=283 | NCT02477826: 2/375 (0.5%) on Ipilimumab (serious AE) |
| Immune-mediated uveitis | 79 | 384.0 285.7–516.0ROR 384.7 · calibrated p 2e-12 ✓ | 203.5 EB05 168.6 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=79 · 100% clinician | not reported in cached trials |
| Immune-mediated hypophysitis | 174 | 336.3 277.1–408.0ROR 337.6 · calibrated p 5e-12 ✓ | 194.2 EB05 171.1 · IC025 +6.7 3/3 methods agree | Labeled adverse reaction exact term | serious n=174 · 100% clinician | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Immune-mediated gastrointestinal disorder | 16 | 308.0 164.4–576.8ROR 308.1 · calibrated p 4e-10 ✓ | 154.0 EB05 100.5 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=16 | not reported in cached trials |
| Endocrine toxicity | 32 | 229.8 150.8–350.2ROR 230.0 · calibrated p 6e-10 ✓ | 142.8 EB05 105.9 · IC025 +4.9 3/3 methods agree | Labeled (related wording) related wording | serious n=32 · 100% clinician | not reported in cached trials |
| Immune-mediated enterocolitis | 1,121 | 228.7 213.1–245.4ROR 234.8 · calibrated p 1e-10 ✓ | 154.9 EB05 147.5 · IC025 +7.1 3/3 methods agree | Labeled adverse reaction exact term | serious n=1,121 · 98% clinician | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Immune-mediated dermatitis | 281 | 210.3 182.9–241.9ROR 211.7 · calibrated p 3e-10 ✓ | 145.2 EB05 131.5 · IC025 +6.7 3/3 methods agree | Labeled (related wording) related wording | serious n=271 · 98% clinician | not reported in cached trials |
| Immune-mediated endocrinopathy | 42 | 206.2 143.7–296.0ROR 206.4 · calibrated p 1e-9 ✓ | 135.9 EB05 104.7 · IC025 +5.2 3/3 methods agree | Labeled (related wording) related wording | serious n=42 · 100% clinician | not reported in cached trials |
| Immune-mediated thyroiditis | 128 | 183.9 150.0–225.3ROR 184.4 · calibrated p 1e-9 ✓ | 130.7 EB05 112.8 · IC025 +6.2 3/3 methods agree | Labeled (related wording) related wording | serious n=128 · 100% clinician | not reported in cached trials |
| Immune-mediated hepatitis | 521 | 176.9 160.1–195.5ROR 179.1 · calibrated p 1e-9 ✓ | 129.0 EB05 120.0 · IC025 +6.7 3/3 methods agree | Labeled adverse reaction exact term | serious n=521 · 97% clinician | NCT02477826: 7/126 (5.6%) on Ipilimumab (serious AE) |
| Immune-mediated hyperthyroidism | 62 | 171.5 128.3–229.1ROR 171.7 · calibrated p 3e-9 ✓ | 122.0 EB05 98.6 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | serious n=62 · 95% clinician | not reported in cached trials |
| Hypopituitarism | 430 | 160.4 143.9–178.8ROR 162.0 · calibrated p 3e-9 ✓ | 119.9 EB05 110.7 · IC025 +6.6 3/3 methods agree | Labeled adverse reaction exact term | serious n=409 | NCT02477826: 5/391 (1.3%) on Ipilimumab (serious AE) |
| Immune-mediated cystitis | 26 | 158.4 101.7–246.7ROR 158.5 · calibrated p 1e-8 ✓ | 110.0 EB05 78.9 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=26 · 100% clinician | not reported in cached trials |
| Autoimmune dermatitis | 34 | 144.8 98.7–212.4ROR 144.9 · calibrated p 2e-8 ✓ | 105.1 EB05 78.7 · IC025 +4.9 3/3 methods agree | Labeled adverse reaction exact term | serious n=33 · ♀ 62% (drug 36%) · 91% clinician | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Adrenalitis | 24 | 142.6 90.4–224.8ROR 142.7 · calibrated p 3e-8 ✓ | 101.5 EB05 71.8 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=24 · 100% clinician | not reported in cached trials |
| Immune-mediated nephritis | 101 | 140.5 112.6–175.3ROR 140.8 · calibrated p 1e-8 ✓ | 106.8 EB05 90.4 · IC025 +5.8 3/3 methods agree | Labeled adverse reaction exact term | serious n=101 · 100% clinician | not reported in cached trials |
| Leukoderma | 44 | 138.4 99.0–193.5ROR 138.5 · calibrated p 2e-8 ✓ | 103.0 EB05 79.9 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=44 · 91% clinician | not reported in cached trials |
| Autoimmune nephritis | 47 | 134.6 97.4–186.0ROR 134.8 · calibrated p 2e-8 ✓ | 101.2 EB05 79.2 · IC025 +5.2 3/3 methods agree | Labeled (related wording) related wording | serious n=47 · 96% clinician | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Immune-mediated adrenal insufficiency | 160 | 131.6 110.5–156.7ROR 132.1 · calibrated p 2e-8 ✓ | 102.3 EB05 89.7 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious n=160 · 100% clinician | not reported in cached trials |
| Fulminant type 1 diabetes mellitus | 213 | 129.1 111.0–150.1ROR 129.7 · calibrated p 2e-8 ✓ | 101.1 EB05 90.2 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=213 · 100% clinician | not reported in cached trials |
| Immune-mediated hepatic disorder | 399 | 129.0 115.6–144.1ROR 130.2 · calibrated p 2e-8 ✓ | 101.5 EB05 93.4 · IC025 +6.3 3/3 methods agree | Labeled (related wording) related wording | serious n=399 · 99% clinician | NCT02477826: 1/185 (0.5%) on Ipilimumab (serious AE) |
| Adrenocorticotropic hormone deficiency | 182 | 129.0 109.5–151.9ROR 129.5 · calibrated p 2e-8 ✓ | 100.9 EB05 89.2 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=182 · 97% clinician | not reported in cached trials |
| Immune-mediated encephalitis | 103 | 128.4 103.3–159.6ROR 128.7 · calibrated p 2e-8 ✓ | 99.7 EB05 84.6 · IC025 +5.8 3/3 methods agree | Labeled (related wording) related wording | serious n=103 · 100% clinician | not reported in cached trials |
| Immune-mediated lung disease | 362 | 127.8 113.9–143.5ROR 128.9 · calibrated p 2e-8 ✓ | 100.7 EB05 92.3 · IC025 +6.3 3/3 methods agree | Labeled (related wording) related wording | serious n=362 · 99% clinician | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Immune-mediated encephalopathy | 18 | 125.5 74.7–210.9ROR 125.6 · calibrated p 1e-7 ✓ | 90.5 EB05 60.5 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=18 | not reported in cached trials |
| Intestinal intraepithelial lymphocytes increased | 13 | 122.7 66.7–225.5ROR 122.7 · calibrated p 3e-7 ✓ | 86.0 EB05 53.5 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | serious n=13 | not reported in cached trials |
| Immune-mediated arthritis | 71 | 116.2 89.7–150.6ROR 116.4 · calibrated p 6e-8 ✓ | 91.6 EB05 75.0 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=71 · 100% clinician | not reported in cached trials |
| Immune-mediated cholangitis | 65 | 115.4 88.1–151.3ROR 115.6 · calibrated p 6e-8 ✓ | 90.9 EB05 73.8 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=65 · 100% clinician | not reported in cached trials |
| Immune-mediated hypothyroidism | 200 | 111.8 95.9–130.3ROR 112.3 · calibrated p 5e-8 ✓ | 90.1 EB05 80.1 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious n=200 · 97% clinician | not reported in cached trials |
| Immune-mediated myocarditis | 280 | 108.7 95.6–123.8ROR 109.5 · calibrated p 6e-8 ✓ | 88.4 EB05 80.0 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=280 · 99% clinician | NCT02477826: 2/126 (1.6%) on Ipilimumab (serious AE) |
| Pituitary enlargement | 37 | 108.6 76.0–155.1ROR 108.7 · calibrated p 1e-7 ✓ | 85.0 EB05 64.4 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=30 | not reported in cached trials |
| Immune-mediated pancreatitis | 67 | 108.6 83.3–141.5ROR 108.7 · calibrated p 1e-7 ✓ | 86.6 EB05 70.6 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=67 · 100% clinician | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Autoimmune arthritis | 28 | 107.8 71.6–162.4ROR 107.9 · calibrated p 2e-7 ✓ | 83.4 EB05 60.5 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious n=28 · 93% clinician | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Immune-mediated neurological disorder | 15 | 107.7 61.6–188.6ROR 107.8 · calibrated p 5e-7 ✓ | 79.6 EB05 51.2 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=15 | not reported in cached trials |
| Immune-mediated myasthenia gravis | 55 | 107.6 80.3–144.1ROR 107.7 · calibrated p 1e-7 ✓ | 85.6 EB05 68.2 · IC025 +5.2 3/3 methods agree | Labeled (related wording) related wording | serious n=55 · 100% clinician | not reported in cached trials |
| Immune-mediated gastritis | 31 | 97.5 66.3–143.4ROR 97.6 · calibrated p 4e-7 ✓ | 77.5 EB05 57.2 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=31 · 100% clinician | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Myocarditis-myositis-myasthenia gravis overlap syndrome | 29 | 93.0 62.5–138.4ROR 93.1 · calibrated p 5e-7 ✓ | 74.4 EB05 54.4 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious n=29 · 100% clinician | not reported in cached trials |
| Vogt-koyanagi-harada disease | 34 | 91.9 63.7–132.6ROR 92.0 · calibrated p 5e-7 ✓ | 74.2 EB05 55.6 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=34 · 100% clinician | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Ipilimumab 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 (14 of 40 signal terms matched).
- NCT02477826 — An Investigational Immuno-therapy Trial of Nivolumab, or Nivolumab Plus Ipilimumab, or Nivolumab Plus Platinum (N=2747, PHASE3; 654 AE terms posted; arms: Part 1-Arm B: Nivo + Ipi; Part 1-Arm A: Nivolumab; Part 1-Arm C: Chemotherapy; Part 1-Arm D: Nivo + Ipi)
- NCT02872116 — Efficacy Study of Nivolumab Plus Ipilimumab or Nivolumab Plus Chemotherapy Against Chemotherapy in Stomach Can (N=2031, PHASE3; 1104 AE terms posted; arms: Nivo + Chemo; Chemo; Nivo + Ipi)
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 |
|---|---|---|---|---|---|---|
| Death | 4,422 | 2.5 2.4–2.6ROR 2.7 · calibrated p 0.736 | 2.5 EB05 2.4 · IC025 +1.3 3/3 methods agree | Outcome field, not a reaction | serious PRR 1.6 | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Malignant neoplasm progression | 3,782 | 18.8 18.2–19.4ROR 20.5 · calibrated p 0.002 ✓ | 18.1 EB05 17.7 · IC025 +4.1 3/3 methods agree | Reporting / coding artifact | serious PRR 12.0 | NCT02477826: 18/126 (14.3%) on Ipilimumab (serious AE) |
| Diarrhoea (diarrhea) | 3,127 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.817 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.4 | NCT02477826: 4/126 (3.2%) on Ipilimumab (serious AE) |
| Off label use (used outside approved label) | 2,501 | 1.4 1.4–1.5ROR 1.4 · calibrated p 0.599 | 1.4 EB05 1.4 · IC025 +0.4 | Reporting / coding artifact | serious PRR 1.4 | not reported in cached trials |
| Colitis | 2,316 | 32.0 30.7–33.3ROR 33.7 · calibrated p 1e-4 ✓ | 30.0 EB05 29.0 · IC025 +4.8 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 20.9 | NCT02477826: 2/375 (0.5%) on Ipilimumab (serious AE) |
| Pyrexia (fever) | 2,056 | 2.9 2.8–3.0ROR 3.0 · calibrated p 0.623 | 2.9 EB05 2.8 · IC025 +1.5 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.2 | NCT02477826: 6/126 (4.8%) on Ipilimumab (serious AE) |
| Rash | 1,805 | 2.0 1.9–2.1ROR 2.1 · calibrated p 0.989 | 2.0 EB05 2.0 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 2.3 | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Fatigue (tiredness) | 1,695 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.352 | 1.1 EB05 1.0 · IC025 +0.0 | Labeled adverse reaction exact term | serious PRR 1.1 | NCT02477826: 3/391 (0.8%) on Ipilimumab (serious AE) |
| Nausea | 1,384 | 0.9 0.8–0.9ROR 0.9 · calibrated p 0.214 | 0.9 EB05 0.8 · IC025 -0.3 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 1.0 | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Intentional product use issue | 1,346 | 7.6 7.2–8.0ROR 7.8 · calibrated p 0.072 | 7.5 EB05 7.1 · IC025 +2.8 3/3 methods agree | Reporting / coding artifact | serious PRR 6.3 | not reported in cached trials |
| Immune-mediated enterocolitis | 1,121 | 228.7 213.1–245.4ROR 234.8 · calibrated p 1e-10 ✓ | 154.9 EB05 147.5 · IC025 +7.1 3/3 methods agree | Labeled adverse reaction exact term | serious n=1,121 · 98% clinician | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Decreased appetite (loss of appetite) | 1,117 | 2.4 2.2–2.5ROR 2.4 · calibrated p 0.857 | 2.4 EB05 2.2 · IC025 +1.1 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.2 | NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE) |
| Hypophysitis | 1,074 | 566.7 519.1–618.7ROR 581.2 · calibrated p 1e-14 ✓ | 259.6 EB05 246.8 · IC025 +7.8 3/3 methods agree | Labeled adverse reaction exact term | serious n=922 | NCT02477826: 2/126 (1.6%) on Ipilimumab (serious AE) |
| Vomiting | 1,051 | 1.1 1.0–1.2ROR 1.1 · calibrated p 0.372 | 1.1 EB05 1.0 · IC025 +0.0 | Labeled adverse reaction exact term | serious PRR 1.0 | NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE) |
| Dyspnoea (shortness of breath) | 1,015 | 0.9 0.8–0.9ROR 0.9 · calibrated p 0.227 | 0.9 EB05 0.8 · IC025 -0.3 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.7 | NCT02477826: 1/126 (0.8%) on Ipilimumab (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.
- Lymphocytic hypophysitis — n=142, PRR 521.6
- Immune-mediated cystitis — n=26, PRR 158.4
- Adrenalitis — n=24, PRR 142.6
- Leukoderma — n=44, PRR 138.4
- Immune-mediated cholangitis — n=65, PRR 115.4
- Pituitary enlargement — n=37, PRR 108.6
✓ A hand-written Bradford Hill causality assessment exists for this drug: Ipilimumab (checkpoint inhibitors) ↔ Immune-mediated colitis.
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 Ipilimumab?
In FDA FAERS, the most frequently co-reported reaction terms for Ipilimumab are diarrhoea, colitis, pyrexia, rash, fatigue, nausea. 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 Ipilimumab have an FDA boxed warning?
No. The FDA label retrieved for Ipilimumab has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Ipilimumab 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 2265ef30-253e-11df-8a39-0800200c9a66, effective 20260820; matched on
openfda.generic_name.exact:"IPILIMUMAB") - 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, 1,131 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
IPILIMUMAB, 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.