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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 FOSAPREPITANT Cause Condition aggravated? 125 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 125 reports of Condition aggravated have been filed in association with FOSAPREPITANT. This represents 25.7% of all adverse event reports for FOSAPREPITANT.

125
Reports of Condition aggravated with FOSAPREPITANT
25.7%
of all FOSAPREPITANT reports
67
Deaths
125
Hospitalizations

How Dangerous Is Condition aggravated From FOSAPREPITANT?

Of the 125 reports, 67 (53.6%) resulted in death, 125 (100.0%) required hospitalization, and 68 (54.4%) 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 FOSAPREPITANT. However, 125 reports have been filed with the FAERS database.

What Other Side Effects Does FOSAPREPITANT Cause?

Dyspnoea (195) Infusion related reaction (167) Hypersensitivity (157) Duodenal ulcer perforation (155) Confusional state (149) Glossodynia (149) Folliculitis (146) Arthralgia (144) Blister (144) Discomfort (144)

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 FOSAPREPITANT Alternatives Have Lower Condition aggravated Risk?

FOSAPREPITANT vs FOSAPREPITANT DIMEGLUMINE FOSAPREPITANT vs FOSCARBIDOPA\FOSLEVODOPA FOSAPREPITANT vs FOSCARNET FOSAPREPITANT vs FOSFOMYCIN FOSAPREPITANT vs FOSFOMYCIN TROMETHAMINE

Related Pages

FOSAPREPITANT Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated FOSAPREPITANT Demographics