Does BENDAMUSTINE Cause Intentional product use issue? 285 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 285 reports of Intentional product use issue have been filed in association with BENDAMUSTINE (VIVIMUSTA). This represents 1.5% of all adverse event reports for BENDAMUSTINE.
285
Reports of Intentional product use issue with BENDAMUSTINE
1.5%
of all BENDAMUSTINE reports
71
Deaths
76
Hospitalizations
How Dangerous Is Intentional product use issue From BENDAMUSTINE?
Of the 285 reports, 71 (24.9%) resulted in death, 76 (26.7%) required hospitalization, and 14 (4.9%) 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 BENDAMUSTINE. However, 285 reports have been filed with the FAERS database.
What Other Side Effects Does BENDAMUSTINE Cause?
Off label use (2,578)
Disease progression (2,456)
Pyrexia (1,322)
Neutropenia (1,256)
Drug ineffective (1,135)
Febrile neutropenia (1,005)
Pneumonia (975)
Thrombocytopenia (967)
Covid-19 (892)
Anaemia (817)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BENDAMUSTINE Alternatives Have Lower Intentional product use issue Risk?
BENDAMUSTINE vs BENDROFLUMETHIAZIDE
BENDAMUSTINE vs BENIDIPINE
BENDAMUSTINE vs BENLYSTA
BENDAMUSTINE vs BENRALIZUMAB
BENDAMUSTINE vs BENSERAZIDE