← All drugs
Drug · FAERS side-effect profile with label screen

Ipilimumab side effects: what 42,905 FDA adverse event reports show

Ipilimumab · Yervoy · 1,131 reaction terms · 114,474 drug–reaction co-reports · data 2026-09-14
Share: X Facebook Reddit Email

Drug class

CTLA-4-directed Blocking Antibody

FDA label (Established Pharmacologic Class)

Brand names

Yervoy

openFDA label

Who reports

42,905 reports · 89% serious · 9,586 with death outcome · 36% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

FDA label, Description section

Boxed warning

None in the current label

How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled adverse reaction 7Labeled (related wording) 24Lab value / disease marker 1Not in label — unassessed 8
What the badges mean

Strongest disproportionality signals

Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,091 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Hypophysitis1,074566.7
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=922NCT02477826: 2/126 (1.6%) on Ipilimumab (serious AE)
Lymphocytic hypophysitis142521.6
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 — unassessedserious n=139 · 96% cliniciannot reported in cached trials
Immune-mediated hypophysitis174336.3
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% clinicianNCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE)
Immune-mediated enterocolitis1,121228.7
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% clinicianNCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE)
Immune-mediated hepatitis521176.9
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% clinicianNCT02477826: 7/126 (5.6%) on Ipilimumab (serious AE)
Hypopituitarism430160.4
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=409NCT02477826: 5/391 (1.3%) on Ipilimumab (serious AE)
Immune-mediated cystitis26158.4
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 — unassessedserious n=26 · 100% cliniciannot reported in cached trials
Autoimmune dermatitis34144.8
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% clinicianNCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE)
Adrenalitis24142.6
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 — unassessedserious n=24 · 100% cliniciannot reported in cached trials
Immune-mediated nephritis101140.5
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% cliniciannot reported in cached trials
Leukoderma44138.4
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 — unassessedserious n=44 · 91% cliniciannot reported in cached trials
Immune-mediated encephalopathy18125.5
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 — unassessedserious n=18not reported in cached trials
Intestinal intraepithelial lymphocytes increased13122.7
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 markerserious n=13not reported in cached trials
Immune-mediated cholangitis65115.4
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 — unassessedserious n=65 · 100% cliniciannot reported in cached trials
Pituitary enlargement37108.6
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 — unassessedserious n=30not reported in cached trials
Immune-mediated neurological disorder15107.7
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 — unassessedserious n=15not 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).

Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Death4,4222.5
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 reactionserious PRR 1.6NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE)
Malignant neoplasm progression3,78218.8
18.2–19.4ROR 20.5 · calibrated p 0.002 ✓
18.1 EB05 17.7 · IC025 +4.1
3/3 methods agree
Reporting / coding artifactserious PRR 12.0NCT02477826: 18/126 (14.3%) on Ipilimumab (serious AE)
Diarrhoea (diarrhea)3,1272.4
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 2.4NCT02477826: 4/126 (3.2%) on Ipilimumab (serious AE)
Off label use (used outside approved label)2,5011.4
1.4–1.5ROR 1.4 · calibrated p 0.599
1.4 EB05 1.4 · IC025 +0.4Reporting / coding artifactserious PRR 1.4not reported in cached trials
Colitis2,31632.0
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 20.9NCT02477826: 2/375 (0.5%) on Ipilimumab (serious AE)
Pyrexia (fever)2,0562.9
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 2.2NCT02477826: 6/126 (4.8%) on Ipilimumab (serious AE)
Rash1,8052.0
1.9–2.1ROR 2.1 · calibrated p 0.989
2.0 EB05 2.0 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.3NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE)
Fatigue (tiredness)1,6951.1
1.0–1.1ROR 1.1 · calibrated p 0.352
1.1 EB05 1.0 · IC025 +0.0Labeled adverse reaction
exact term
serious PRR 1.1NCT02477826: 3/391 (0.8%) on Ipilimumab (serious AE)
Nausea1,3840.9
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 1.0NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE)
Intentional product use issue1,3467.6
7.2–8.0ROR 7.8 · calibrated p 0.072
7.5 EB05 7.1 · IC025 +2.8
3/3 methods agree
Reporting / coding artifactserious PRR 6.3not reported in cached trials
Immune-mediated enterocolitis1,121228.7
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% clinicianNCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE)
Decreased appetite (loss of appetite)1,1172.4
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 2.2NCT02477826: 1/391 (0.3%) on Ipilimumab (serious AE)
Hypophysitis1,074566.7
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=922NCT02477826: 2/126 (1.6%) on Ipilimumab (serious AE)
Vomiting1,0511.1
1.0–1.2ROR 1.1 · calibrated p 0.372
1.1 EB05 1.0 · IC025 +0.0Labeled adverse reaction
exact term
serious PRR 1.0NCT02477826: 1/126 (0.8%) on Ipilimumab (serious AE)
Dyspnoea (shortness of breath)1,0150.9
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 0.7NCT02477826: 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.

✓ 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

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.