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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.

SEAGEN INC.: 4 Drugs and 17,357 Adverse Event Reports

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SEAGEN INC. manufactures 4 drugs with a combined 17,357 adverse event reports in the FDA FAERS database. Their most reported drug is BRENTUXIMAB VEDOTIN.

4
Drugs
17,357
Combined Reports
2,856
Total Deaths
6,244
Total Hospitalizations

All SEAGEN INC. Drugs & Safety Profiles

Drug Brand Name Reports Deaths Death Rate Hosp.
BRENTUXIMAB VEDOTIN ADCETRIS 9,724 1,922 19.8% 3,781
TUCATINIB TUKYSA 6,042 640 10.6% 1,717
ENFORTUMAB VEDOTIN PADCEV EJFV 1,425 278 19.5% 645
TISOTUMAB VEDOTIN TIVDAK 166 16 9.6% 101