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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.

Does BORTEZOMIB Cause Intentional product use issue? 1,361 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,361 reports of Intentional product use issue have been filed in association with BORTEZOMIB (bortezomib). This represents 2.9% of all adverse event reports for BORTEZOMIB.

1,361
Reports of Intentional product use issue with BORTEZOMIB
2.9%
of all BORTEZOMIB reports
250
Deaths
126
Hospitalizations

How Dangerous Is Intentional product use issue From BORTEZOMIB?

Of the 1,361 reports, 250 (18.4%) resulted in death, 126 (9.3%) required hospitalization, and 26 (1.9%) were considered life-threatening.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BORTEZOMIB. However, 1,361 reports have been filed with the FAERS database.

What Other Side Effects Does BORTEZOMIB Cause?

Plasma cell myeloma (6,683) Off label use (4,754) Neuropathy peripheral (4,067) Drug ineffective (2,730) Diarrhoea (2,244) Thrombocytopenia (2,082) Death 503 Service Unavailable

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