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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Programmed Death Receptor-1-directed Antibody Interactions [MoA] — Common Side Effects

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Side Effect Total Reports Drugs Deaths Hosp. Life-Threat.
Malignant neoplasm progression 19,834 5 10,428 7,864 1,418
Death 19,612 6 19,600 2,139 337
Off label use 11,400 7 2,803 3,579 690
Diarrhoea 10,680 7 1,529 5,585 644
Fatigue 8,924 6 1,079 3,198 328
Pyrexia 8,462 7 1,244 5,946 638
Rash 6,811 6 693 2,539 364
Nausea 6,693 7 953 3,343 339
Decreased appetite 6,220 6 1,073 3,184 335
Dyspnoea 5,491 6 1,305 3,389 559
Hypothyroidism 5,319 6 638 2,112 332
Pneumonia 5,258 6 1,836 3,742 691
Asthenia 5,028 7 936 2,613 342
Anaemia 4,971 6 963 2,791 410
Pneumonitis 4,934 6 1,357 2,620 574
Product use in unapproved indication 4,599 6 1,191 1,218 187
Interstitial lung disease 4,503 6 1,611 2,612 571
Colitis 4,476 7 684 2,580 340
Vomiting 4,451 7 756 2,801 349
Acute kidney injury 4,419 6 775 3,386 650
Intentional product use issue 4,097 3 1,755 1,035 167
Myelosuppression 3,991 5 106 1,941 193
Hypertension 3,848 6 551 1,681 197
Drug ineffective 3,805 5 927 1,040 240
Malaise 3,706 5 672 2,034 195
Pruritus 3,660 6 267 1,184 112
Neutropenia 3,511 6 453 1,257 279
Thrombocytopenia 3,381 6 543 1,453 333
Weight decreased 3,345 6 367 1,407 162
Arthralgia 3,334 5 267 1,089 98
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