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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.

Exelixis, Inc.: 1 Drugs and 39,270 Adverse Event Reports

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Exelixis, Inc. manufactures 1 drugs with a combined 39,270 adverse event reports in the FDA FAERS database. Their most reported drug is CABOZANTINIB S-MALATE.

1
Drugs
39,270
Combined Reports
4,203
Total Deaths
6,193
Total Hospitalizations

All Exelixis, Inc. Drugs & Safety Profiles

Drug Brand Name Reports Deaths Death Rate Hosp.
CABOZANTINIB S-MALATE CABOMETYX 39,270 4,203 10.7% 6,193