Pembrolizumab side effects: what 104,591 FDA adverse event reports show
Drug class
Programmed Death Receptor-1 Blocking Antibody
Brand names
Keytruda
Who reports
104,591 reports · 87% serious · 18,742 with death outcome · 50% female
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.
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.
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.
- 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.
- 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). 1,236 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 |
|---|---|---|---|---|---|---|
| Immune-mediated pancytopenia | 35 | 626.3 318.1–1,233.1ROR 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 — unassessed | serious n=35 · ♀ 100% (drug 50%) · 100% clinician | not reported in cached trials |
| Immune-mediated renal disorder | 244 | 338.2 275.0–415.9ROR 339.0 · calibrated p 5e-12 ✓ | 123.9 EB05 111.4 · IC025 +6.4 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 4.2 (3.4–5.4) | Labeled (related wording) related wording | serious n=243 · 100% clinician | not reported in cached trials |
| Immune-mediated hypothyroidism | 664 | 329.2 290.8–372.7ROR 331.3 · calibrated p 4e-12 ✓ | 123.4 EB05 115.7 · IC025 +6.7 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 3.4 (3.0–3.9) | Labeled (related wording) related wording | serious n=664 · 96% clinician | NCT05665595: 2/797 (0.3%) on Pembrolizumab (serious AE) |
| Immune-mediated hyperthyroidism | 147 | 325.1 249.9–423.0ROR 325.6 · calibrated p 9e-12 ✓ | 121.3 EB05 105.7 · IC025 +6.2 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 3.4 (2.5–4.5) | Labeled (related wording) related wording | serious n=147 · ♀ 74% (drug 50%) · 91% clinician | not reported in cached trials |
| Immune-mediated gastritis | 110 | 292.6 217.9–392.8ROR 292.9 · calibrated p 3e-11 ✓ | 115.9 EB05 98.9 · IC025 +6.0 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 3.2 (2.4–4.5) | Labeled (related wording) related wording | serious n=110 · 100% clinician | not reported in cached trials |
| Immune-mediated adrenal insufficiency | 445 | 292.0 252.2–338.0ROR 293.2 · calibrated p 1e-11 ✓ | 117.6 EB05 108.7 · IC025 +6.5 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.8 (2.4–3.3) | Labeled (related wording) related wording | serious n=444 · 100% clinician | not reported in cached trials |
| Immune-mediated adverse reaction | 831 | 267.7 241.2–297.1ROR 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=819 | not reported in cached trials |
| Immune-mediated neurological disorder | 47 | 264.3 170.6–409.4ROR 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 — unassessed | serious n=47 · 100% clinician | not reported in cached trials |
| Immune-mediated endocrinopathy | 77 | 240.6 172.5–335.6ROR 240.8 · calibrated p 2e-10 ✓ | 106.0 EB05 87.6 · IC025 +5.6 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.3 (1.6–3.2) | Labeled (related wording) related wording | serious n=77 · 100% clinician | not reported in cached trials |
| Immune-mediated hepatic disorder | 1,022 | 232.6 212.5–254.6ROR 234.8 · calibrated p 1e-10 ✓ | 106.9 EB05 101.5 · IC025 +6.6 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.7 (2.4–2.9) | Labeled (related wording) related wording | serious n=1,022 · 93% clinician | not reported in cached trials |
| Immune-mediated thyroiditis | 242 | 215.5 179.6–258.6ROR 216.0 · calibrated p 3e-10 ✓ | 102.6 EB05 92.2 · IC025 +6.2 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.0 (1.7–2.4) | Labeled (related wording) related wording | serious n=241 · 100% clinician | not reported in cached trials |
| Tumour hyperprogression | 118 | 203.7 157.5–263.5ROR 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 — unassessed | serious n=118 · 92% clinician | not reported in cached trials |
| Immune-mediated pancreatitis | 184 | 201.2 163.9–247.1ROR 201.6 · calibrated p 5e-10 ✓ | 99.0 EB05 87.6 · IC025 +6.1 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.3 (1.9–2.9) | Labeled (related wording) related wording | serious n=184 · 100% clinician | not reported in cached trials |
| Immune-mediated pneumonitis | 117 | 196.8 152.3–254.3ROR 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=117 | not reported in cached trials |
| Immune-mediated arthritis | 180 | 191.5 156.0–235.1ROR 191.8 · calibrated p 8e-10 ✓ | 96.6 EB05 85.3 · IC025 +6.0 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.1 (1.7–2.6) | Labeled (related wording) related wording | serious n=180 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Immune-mediated neuropathy | 71 | 191.4 138.1–265.4ROR 191.6 · calibrated p 2e-9 ✓ | 95.1 EB05 77.9 · IC025 +5.5 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.9 (2.0–4.3) | Labeled (related wording) related wording | serious n=71 · 100% clinician | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Immune-mediated dermatitis | 453 | 189.3 166.4–215.3ROR 190.1 · calibrated p 7e-10 ✓ | 96.6 EB05 89.4 · IC025 +6.3 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.0 (1.7–2.3) | Labeled (related wording) related wording | serious n=428 · 96% clinician | not reported in cached trials |
| Immune-mediated myocarditis | 734 | 184.0 166.5–203.5ROR 185.3 · calibrated p 8e-10 ✓ | 95.4 EB05 89.7 · IC025 +6.4 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.2 (1.9–2.4) | Labeled (related wording) related wording | serious n=734 · 98% clinician | NCT05665595: 4/796 (0.5%) on Pembrolizumab (serious AE) |
| Transitional cell carcinoma metastatic | 51 | 170.1 117.0–247.5ROR 170.2 · calibrated p 5e-9 ✓ | 88.8 EB05 70.1 · IC025 +5.1 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug | Labeled (related wording) related wording | serious n=51 · ♀ 0% (drug 50%) · 100% clinician | not reported in cached trials |
| Immune-mediated myasthenia gravis | 139 | 168.9 134.7–211.8ROR 169.1 · calibrated p 3e-9 ✓ | 90.3 EB05 78.3 · IC025 +5.8 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.9 (1.5–2.5) | Labeled (related wording) related wording | serious n=139 · 100% clinician | not reported in cached trials |
| Tumour pseudoprogression | 464 | 150.2 133.1–169.5ROR 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 — unassessed | serious n=464 | not reported in cached trials |
| Myocarditis-myositis-myasthenia gravis overlap syndrome | 77 | 148.6 110.5–199.7ROR 148.7 · calibrated p 1e-8 ✓ | 83.4 EB05 68.9 · IC025 +5.4 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.5 (1.8–3.6) | Labeled (related wording) related wording | serious n=77 · 100% clinician | not reported in cached trials |
| Immune-mediated hypophysitis | 176 | 140.3 115.6–170.2ROR 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% clinician | NCT05665595: 2/796 (0.3%) on Pembrolizumab (serious AE) |
| Immune-mediated encephalitis | 203 | 139.7 116.7–167.2ROR 140.0 · calibrated p 1e-8 ✓ | 81.5 EB05 72.5 · IC025 +5.9 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.5 (1.3–1.8) | Labeled (related wording) related wording | serious n=203 · 100% clinician | NCT05665595: 2/797 (0.3%) on Pembrolizumab (serious AE) |
| Immune-mediated cystitis | 43 | 136.5 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 — unassessed | serious n=43 · ♀ 100% (drug 50%) · 100% clinician | not reported in cached trials |
| Immune-mediated nephritis | 180 | 132.7 109.9–160.3ROR 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% clinician | NCT03675737: 1/785 (0.1%) on Pembrolizumab (serious AE) |
| Immune-mediated cholangitis | 134 | 130.6 105.0–162.4ROR 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 — unassessed | serious n=134 · 100% clinician | not reported in cached trials |
| Adrenocorticotropic hormone deficiency | 337 | 126.6 110.4–145.1ROR 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=335 | not reported in cached trials |
| Malignant neoplasm oligoprogression | 66 | 121.4 89.3–165.0ROR 121.5 · calibrated p 5e-8 ✓ | 73.9 EB05 60.1 · IC025 +5.2 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug | Labeled (related wording) related wording | serious n=66 · 100% clinician | not reported in cached trials |
| Immune-mediated lung disease | 646 | 117.8 106.9–129.9ROR 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% clinician | NCT03675737: 2/785 (0.3%) on Pembrolizumab; 1/787 (0.1%) control (serious AE) |
| Immune-mediated hepatitis | 693 | 109.6 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% clinician | NCT05665595: 4/796 (0.5%) on Pembrolizumab (serious AE) |
| Autoimmune hypothyroidism | 82 | 108.3 82.7–141.8ROR 108.4 · calibrated p 1e-7 ✓ | 69.1 EB05 57.5 · IC025 +5.3 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 2.8 (1.9–3.9) | Labeled (related wording) related wording | serious n=82 · 100% clinician | not reported in cached trials |
| Autoimmune lung disease | 39 | 102.4 69.5–150.7ROR 102.4 · calibrated p 3e-7 ✓ | 65.6 EB05 50.1 · IC025 +4.7 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: only this drug | Labeled (related wording) related wording | serious n=39 · ♀ 0% (drug 50%) · 100% clinician | not reported in cached trials |
| Immunotoxicity | 37 | 98.4 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 — unassessed | serious n=36 · 100% clinician | not reported in cached trials |
| Silent thyroiditis | 46 | 94.3 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 — unassessed | serious n=42 · ♀ 100% (drug 50%) · 100% clinician | not reported in cached trials |
| Adrenalitis | 34 | 94.3 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 — unassessed | serious n=34 · 100% clinician | not reported in cached trials |
| Immune-mediated enterocolitis | 1,091 | 89.9 83.7–96.5ROR 90.8 · calibrated p 2e-7 ✓ | 62.0 EB05 58.9 · IC025 +5.8 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 1.1 (1.0–1.2) | Labeled (related wording) related wording | serious n=1,088 · 93% clinician | NCT05665595: 2/796 (0.3%) on Pembrolizumab (serious AE) |
| Immune-mediated uveitis | 50 | 76.9 55.5–106.6ROR 76.9 · calibrated p 1e-6 ✓ | 54.5 EB05 42.9 · IC025 +4.7 3/3 methods agree vs other Programmed Death Receptor-1 Blocking Antibodys: PRR 0.7 (0.5–0.9) | Labeled (related wording) related wording | serious n=50 · 100% clinician | not reported in cached trials |
| Pseudocellulitis | 58 | 75.6 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 — unassessed | serious n=56 · ♀ 0% (drug 50%) · 100% clinician | not reported in cached trials |
| Urogenital fistula | 62 | 72.2 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 — unassessed | serious n=61 · ♀ 100% (drug 50%) · 100% clinician | not 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Interstitial lung disease | 4,979 | 10.910.6–11.2 | signal |
| Neutropenia / agranulocytosis | 4,847 | 4.03.9–4.1 | signal |
| Severe cutaneous reaction | 1,341 | 3.73.5–3.9 | signal |
| Thrombocytopenia | 3,651 | 3.43.3–3.5 | signal |
| Liver injury | 4,520 | 3.02.9–3.1 | signal |
| Rhabdomyolysis / myopathy | 1,157 | 2.92.7–3.1 | signal |
| Hyponatraemia | 1,022 | 2.62.4–2.7 | signal |
| Kidney injury | 5,710 | 2.52.5–2.6 | signal |
| Anaemia | 2,997 | 2.01.9–2.1 | raised |
| Pancreatitis | 802 | 2.01.9–2.1 | raised |
| Heart failure | 1,359 | 1.51.4–1.6 | raised |
| Venous thromboembolism | 1,462 | 1.41.3–1.4 | raised |
| Serious infection | 5,150 | 1.31.3–1.4 | raised |
| Hyperglycaemia / diabetes | 1,850 | 1.11.0–1.1 | raised |
| Opportunistic infection | 724 | 1.11.0–1.1 | no difference |
| Stroke | 1,180 | 0.90.9–1.0 | no 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).
- NCT05665595 — A Study of Adjuvant Pembrolizumab/Vibostolimab (MK-7684A) Versus Pembrolizumab for Resected High-Risk Melanoma (N=1594, PHASE3; 289 AE terms posted; arms: Pembrolizumab/Vibostolimab; Pembrolizumab)
- NCT03675737 — Pembrolizumab (MK-3475) Plus Chemotherapy Versus Placebo Plus Chemotherapy in Participants Gastric or Gastroes (N=1579, PHASE3; 401 AE terms posted; arms: Pembrolizumab + Chemotherapy (FP or CAPO; Placebo + Chemotherapy (FP or CAPOX Regi; Pembrolizumab Second Course)
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 |
|---|---|---|---|---|---|---|
| Malignant neoplasm progression | 12,012 | 26.7 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 artifact | age-adj. PRR 23.4 · serious PRR 15.8 | not reported in cached trials |
| Death | 5,848 | 1.4 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 reaction | age-adj. PRR 1.1 · serious PRR 0.9 | NCT05665595: 2/796 (0.3%) on Pembrolizumab (serious AE) |
| Diarrhoea (diarrhea) | 5,719 | 1.8 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 1.7 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Fatigue (tiredness) | 5,112 | 1.3 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 1.2 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Off label use (used outside approved label) | 4,755 | 1.1 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 artifact | age-adj. PRR 1.0 · serious PRR 1.1 | not reported in cached trials |
| Pyrexia (fever) | 3,870 | 2.3 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 1.8 | NCT05665595: 5/797 (0.6%) on Pembrolizumab (serious AE) |
| Rash | 3,717 | 1.7 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 1.9 | NCT05665595: 3/797 (0.4%) on Pembrolizumab (serious AE) |
| Nausea | 3,563 | 0.9 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 1.0 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Product use in unapproved indication | 3,541 | 2.9 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 artifact | age-adj. PRR 2.5 · serious PRR 2.8 | not reported in cached trials |
| Decreased appetite (loss of appetite) | 3,305 | 2.9 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 2.5 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Hypertension (high blood pressure) | 3,231 | 3.1 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 2.3 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Hypothyroidism | 2,917 | 20.1 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 12.8 | NCT05665595: 2/797 (0.3%) on Pembrolizumab (serious AE) |
| Asthenia (weakness) | 2,774 | 1.5 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 1.2 | NCT05665595: 1/796 (0.1%) on Pembrolizumab (serious AE) |
| Drug ineffective (drug did not work) | 2,575 | 0.4 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 artifact | age-adj. PRR 0.5 · serious PRR 0.6 | not reported in cached trials |
| Product use issue | 2,565 | 2.8 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 artifact | age-adj. PRR 2.3 · serious PRR 2.8 | not 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.
- Immune-mediated pancytopenia — n=35, PRR 626.3
- Immune-mediated neurological disorder — n=47, PRR 264.3
- Tumour hyperprogression — n=118, PRR 203.7
- Tumour pseudoprogression — n=464, PRR 150.2
- Immune-mediated cystitis — n=43, PRR 136.5
- Immune-mediated cholangitis — n=134, PRR 130.6
- Immunotoxicity — n=37, PRR 98.4
- Silent thyroiditis — n=46, PRR 94.3
- Adrenalitis — n=34, PRR 94.3
- Pseudocellulitis — n=58, PRR 75.6
✓ 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
- FDA label via openFDA (set ID 9333c79b-d487-4538-a9f0-71b91a02b287, effective 20260710; matched on
openfda.generic_name.exact:"PEMBROLIZUMAB") - 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, 1,276 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
PEMBROLIZUMAB, 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.