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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 GEMCITABINE Cause Performance status decreased? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Performance status decreased have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.1% of all adverse event reports for GEMCITABINE.

28
Reports of Performance status decreased with GEMCITABINE
0.1%
of all GEMCITABINE reports
15
Deaths
5
Hospitalizations

How Dangerous Is Performance status decreased From GEMCITABINE?

Of the 28 reports, 15 (53.6%) resulted in death, 5 (17.9%) required hospitalization, and 1 (3.6%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GEMCITABINE. However, 28 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 Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68)

Which GEMCITABINE Alternatives Have Lower Performance status decreased Risk?

GEMCITABINE vs GEMCITABINE\GEMCITABINE GEMCITABINE vs GEMFIBROZIL GEMCITABINE vs GEMTUZUMAB OZOGAMICIN GEMCITABINE vs GEMZAR GEMCITABINE vs GENTAMICIN

Related Pages

GEMCITABINE Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased GEMCITABINE Demographics