Does GEMCITABINE Cause Condition aggravated? 389 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 389 reports of Condition aggravated have been filed in association with GEMCITABINE (Gemcitabine). This represents 1.2% of all adverse event reports for GEMCITABINE.
389
Reports of Condition aggravated with GEMCITABINE
1.2%
of all GEMCITABINE reports
76
Deaths
204
Hospitalizations
How Dangerous Is Condition aggravated From GEMCITABINE?
Of the 389 reports, 76 (19.5%) resulted in death, 204 (52.4%) required hospitalization, and 49 (12.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GEMCITABINE. However, 389 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which GEMCITABINE Alternatives Have Lower Condition aggravated Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN