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Pembrolizumab side effects: what 104,591 FDA adverse event reports show

Pembrolizumab · Keytruda · 1,276 reaction terms · 290,924 drug–reaction co-reports · data 2026-09-14
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Drug class

Programmed Death Receptor-1 Blocking Antibody

FDA label (Established Pharmacologic Class) · compare the class

Brand names

Keytruda

openFDA label

Who reports

104,591 reports · 87% serious · 18,742 with death outcome · 50% female

openFDA FAERS counts, all years, deduplication not applied

Used for

KEYTRUDA is a programmed death receptor-1 (PD-1)-blocking antibody indicated: Melanoma for the treatment of patients with unresectable or metastatic melanoma. ( 1.1 ) for the adjuvant treatment of adult and pediatric (12 years and older) patients with Stage IIB, IIC, or III melanoma following complete resection.

FDA label, Indications and Usage

What it is

Pembrolizumab is a programmed death receptor-1 (PD 1)-blocking antibody. Pembrolizumab is a humanized monoclonal IgG4 kappa antibody with an approximate molecular weight of 149 kDa. Pembrolizumab is produced in recombinant Chinese hamster ovary (CHO) cells.

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 6Labeled (related wording) 22Likely indication confounding 1Not in label — unassessed 11
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). 1,236 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
Immune-mediated pancytopenia35626.3
318.1–1,233.1ROR 626.5 · calibrated p 2e-12 ✓
139.2 EB05 104.7 · IC025 +5.0
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug
Not in label — unassessedserious n=35 · ♀ 100% (drug 50%) · 100% cliniciannot reported in cached trials
Immune-mediated adverse reaction831267.7
241.2–297.1ROR 269.8 · calibrated p 3e-11 ✓
113.7 EB05 107.4 · IC025 +6.6
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 6.0 (5.2–6.9)
Labeled adverse reaction
exact term
serious n=819not reported in cached trials
Immune-mediated neurological disorder47264.3
170.6–409.4ROR 264.4 · calibrated p 2e-10 ✓
108.5 EB05 84.9 · IC025 +5.2
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug
Not in label — unassessedserious n=47 · 100% cliniciannot reported in cached trials
Tumour hyperprogression118203.7
157.5–263.5ROR 204.0 · calibrated p 6e-10 ✓
99.0 EB05 84.9 · IC025 +5.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 6.5 (4.4–9.7)
Not in label — unassessedserious n=118 · 92% cliniciannot reported in cached trials
Immune-mediated pneumonitis117196.8
152.3–254.3ROR 197.1 · calibrated p 8e-10 ✓
97.4 EB05 83.5 · IC025 +5.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.3 (1.7–3.0)
Labeled adverse reaction
exact term
serious n=117not reported in cached trials
Tumour pseudoprogression464150.2
133.1–169.5ROR 150.9 · calibrated p 5e-9 ✓
85.3 EB05 79.0 · IC025 +6.1
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 3.5 (2.9–4.1)
Not in label — unassessedserious n=464not reported in cached trials
Immune-mediated hypophysitis176140.3
115.6–170.2ROR 140.5 · calibrated p 1e-8 ✓
81.6 EB05 72.0 · IC025 +5.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.4 (1.1–1.7)
Labeled adverse reaction
exact term
serious n=176 · 100% clinicianNCT05665595: 2/796 (0.3%) on Pembrolizumab (serious AE)
Immune-mediated cystitis43136.5
92.5–201.4ROR 136.6 · calibrated p 3e-8 ✓
78.3 EB05 60.6 · IC025 +4.9
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.0–2.2)
Not in label — unassessedserious n=43 · ♀ 100% (drug 50%) · 100% cliniciannot reported in cached trials
Immune-mediated nephritis180132.7
109.9–160.3ROR 132.9 · calibrated p 2e-8 ✓
79.0 EB05 69.8 · IC025 +5.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.8 (1.4–2.2)
Labeled adverse reaction
exact term
serious n=180 · 95% clinicianNCT03675737: 1/785 (0.1%) on Pembrolizumab (serious AE)
Immune-mediated cholangitis134130.6
105.0–162.4ROR 130.7 · calibrated p 2e-8 ✓
78.1 EB05 67.6 · IC025 +5.6
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.3 (1.1–1.7)
Not in label — unassessedserious n=134 · 100% cliniciannot reported in cached trials
Adrenocorticotropic hormone deficiency337126.6
110.4–145.1ROR 127.0 · calibrated p 2e-8 ✓
77.1 EB05 70.4 · IC025 +5.9
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.3–1.7)
Likely indication confounding
shares a disease stem with the indications wording
serious n=335not reported in cached trials
Immune-mediated lung disease646117.8
106.9–129.9ROR 118.6 · calibrated p 3e-8 ✓
73.9 EB05 69.3 · IC025 +6.0
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.3 (1.2–1.5)
Labeled adverse reaction
exact term
serious n=646 · 96% clinicianNCT03675737: 2/785 (0.3%) on Pembrolizumab; 1/787 (0.1%) control (serious AE)
Immune-mediated hepatitis693109.6
99.9–120.2ROR 110.3 · calibrated p 6e-8 ✓
70.6 EB05 66.3 · IC025 +5.9
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.2 (1.1–1.4)
Labeled adverse reaction
exact term
serious n=688 · 93% clinicianNCT05665595: 4/796 (0.5%) on Pembrolizumab (serious AE)
Immunotoxicity3798.4
66.3–146.0ROR 98.5 · calibrated p 3e-7 ✓
63.9 EB05 48.4 · IC025 +4.6
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug
Not in label — unassessedserious n=36 · 100% cliniciannot reported in cached trials
Silent thyroiditis4694.3
66.4–134.0ROR 94.4 · calibrated p 4e-7 ✓
62.5 EB05 48.8 · IC025 +4.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.1 (1.3–3.2)
Not in label — unassessedserious n=42 · ♀ 100% (drug 50%) · 100% cliniciannot reported in cached trials
Adrenalitis3494.3
62.6–141.9ROR 94.3 · calibrated p 5e-7 ✓
61.9 EB05 46.4 · IC025 +4.5
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.6 (1.0–2.6)
Not in label — unassessedserious n=34 · 100% cliniciannot reported in cached trials
Pseudocellulitis5875.6
55.9–102.3ROR 75.6 · calibrated p 1e-6 ✓
54.0 EB05 43.3 · IC025 +4.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug
Not in label — unassessedserious n=56 · ♀ 0% (drug 50%) · 100% cliniciannot reported in cached trials
Urogenital fistula6272.2
54.0–96.6ROR 72.3 · calibrated p 2e-6 ✓
52.3 EB05 42.3 · IC025 +4.8
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug
Not in label — unassessedserious n=61 · ♀ 100% (drug 50%) · 100% cliniciannot 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.

ConceptReportsPRR 95% CIReading
Interstitial lung disease4,97910.910.6–11.2signal
Neutropenia / agranulocytosis4,8474.03.9–4.1signal
Severe cutaneous reaction1,3413.73.5–3.9signal
Thrombocytopenia3,6513.43.3–3.5signal
Liver injury4,5203.02.9–3.1signal
Rhabdomyolysis / myopathy1,1572.92.7–3.1signal
Hyponatraemia1,0222.62.4–2.7signal
Kidney injury5,7102.52.5–2.6signal
Anaemia2,9972.01.9–2.1raised
Pancreatitis8022.01.9–2.1raised
Heart failure1,3591.51.4–1.6raised
Venous thromboembolism1,4621.41.3–1.4raised
Serious infection5,1501.31.3–1.4raised
Hyperglycaemia / diabetes1,8501.11.0–1.1raised
Opportunistic infection7241.11.0–1.1no difference
Stroke1,1800.90.9–1.0no difference

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Pembrolizumab 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 (10 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
Malignant neoplasm progression12,01226.7
26.2–27.2ROR 30.0 · calibrated p 3e-4 ✓
23.6 EB05 23.3 · IC025 +4.5
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.9 (1.9–1.9)
Reporting / coding artifactage-adj. PRR 23.4 · serious PRR 15.8not reported in cached trials
Death5,8481.4
1.3–1.4ROR 1.4 · calibrated p 0.565
1.4 EB05 1.3 · IC025 +0.4
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 0.6 (0.6–0.6)
Outcome field, not a reactionage-adj. PRR 1.1 · serious PRR 0.9NCT05665595: 2/796 (0.3%) on Pembrolizumab (serious AE)
Diarrhoea (diarrhea)5,7191.8
1.7–1.8ROR 1.8 · calibrated p 0.851
1.8 EB05 1.7 · IC025 +0.8
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.4 (1.3–1.4)
Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.7NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Fatigue (tiredness)5,1121.3
1.3–1.4ROR 1.3 · calibrated p 0.533
1.3 EB05 1.3 · IC025 +0.4
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.4–1.5)
Labeled adverse reaction
exact term
age-adj. PRR 1.2 · serious PRR 1.2NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Off label use (used outside approved label)4,7551.1
1.1–1.1ROR 1.1 · calibrated p 0.375
1.1 EB05 1.1 · IC025 +0.1
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 0.8 (0.8–0.8)
Reporting / coding artifactage-adj. PRR 1.0 · serious PRR 1.1not reported in cached trials
Pyrexia (fever)3,8702.3
2.2–2.3ROR 2.3 · calibrated p 0.901
2.2 EB05 2.2 · IC025 +1.1
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.2 (1.1–1.2)
Labeled adverse reaction
exact term
age-adj. PRR 2.0 · serious PRR 1.8NCT05665595: 5/797 (0.6%) on Pembrolizumab (serious AE)
Rash3,7171.7
1.7–1.8ROR 1.8 · calibrated p 0.801
1.7 EB05 1.7 · IC025 +0.7
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.5–1.6)
Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.9NCT05665595: 3/797 (0.4%) on Pembrolizumab (serious AE)
Nausea3,5630.9
0.9–0.9ROR 0.9 · calibrated p 0.244
0.9 EB05 0.9 · IC025 -0.2
PRR-only: not supported by EBGM or IC
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.4 (1.3–1.5)
Labeled adverse reaction
exact term
age-adj. PRR 0.9 · serious PRR 1.0NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Product use in unapproved indication3,5412.9
2.8–3.0ROR 3.0 · calibrated p 0.626
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 3.8 (3.6–4.1)
Reporting / coding artifactage-adj. PRR 2.5 · serious PRR 2.8not reported in cached trials
Decreased appetite (loss of appetite)3,3052.9
2.8–3.0ROR 2.9 · calibrated p 0.643
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.4 (1.3–1.4)
Labeled adverse reaction
exact term
age-adj. PRR 2.4 · serious PRR 2.5NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Hypertension (high blood pressure)3,2313.1
3.0–3.2ROR 3.2 · calibrated p 0.578
3.1 EB05 3.0 · IC025 +1.6
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.9 (2.7–3.0)
Labeled adverse reaction
exact term
age-adj. PRR 2.8 · serious PRR 2.3NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Hypothyroidism2,91720.1
19.4–20.9ROR 20.7 · calibrated p 0.002 ✓
18.4 EB05 17.8 · IC025 +4.1
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.4–1.6)
Labeled adverse reaction
exact term
age-adj. PRR 18.0 · serious PRR 12.8NCT05665595: 2/797 (0.3%) on Pembrolizumab (serious AE)
Asthenia (weakness)2,7741.5
1.4–1.5ROR 1.5 · calibrated p 0.639
1.5 EB05 1.4 · IC025 +0.5
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.4–1.6)
Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.2NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE)
Drug ineffective (drug did not work)2,5750.4
0.4–0.4ROR 0.4 · calibrated p 0.018 ✓
0.4 EB05 0.4 · IC025 -1.4
PRR-only: not supported by EBGM or IC
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.7 (1.6–1.8)
Reporting / coding artifactage-adj. PRR 0.5 · serious PRR 0.6not reported in cached trials
Product use issue2,5652.8
2.7–2.9ROR 2.8 · calibrated p 0.688
2.7 EB05 2.7 · IC025 +1.4
3/3 methods agree
vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 6.5 (5.9–7.0)
Reporting / coding artifactage-adj. PRR 2.3 · serious PRR 2.8not reported in cached trials

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: Pembrolizumab (checkpoint inhibitors) ↔ Hypothyroidism.

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 Pembrolizumab?

In FDA FAERS, the most frequently co-reported reaction terms for Pembrolizumab are diarrhoea, fatigue, pyrexia, rash, nausea, decreased appetite. 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 Pembrolizumab have an FDA boxed warning?

No. The FDA label retrieved for Pembrolizumab has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Pembrolizumab 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.