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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 Hypersensitivity? 161 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 161 reports of Hypersensitivity have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.5% of all adverse event reports for GEMCITABINE.

161
Reports of Hypersensitivity with GEMCITABINE
0.5%
of all GEMCITABINE reports
13
Deaths
51
Hospitalizations

How Dangerous Is Hypersensitivity From GEMCITABINE?

Of the 161 reports, 13 (8.1%) resulted in death, 51 (31.7%) required hospitalization, and 14 (8.7%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for GEMCITABINE.

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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which GEMCITABINE Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

GEMCITABINE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity GEMCITABINE Demographics