Does GEMCITABINE Cause Intentional product use issue? 151 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 151 reports of Intentional product use issue have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.5% of all adverse event reports for GEMCITABINE.
151
Reports of Intentional product use issue with GEMCITABINE
0.5%
of all GEMCITABINE reports
34
Deaths
47
Hospitalizations
How Dangerous Is Intentional product use issue From GEMCITABINE?
Of the 151 reports, 34 (22.5%) resulted in death, 47 (31.1%) required hospitalization, and 2 (1.3%) 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 GEMCITABINE. However, 151 reports have been filed with the FAERS database.
What Other Side Effects Does GEMCITABINE Cause?
Off label use (3,319)
Disease progression (3,123)
Thrombocytopenia (2,320)
Drug ineffective (2,003)
Malignant neoplasm progression (1,962)
Neutropenia (1,892)
Anaemia (1,745)
Pyrexia (1,511)
Nausea (1,336)
Myelosuppression (1,197)
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 GEMCITABINE Alternatives Have Lower Intentional product use issue Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN