Does FOSAPREPITANT Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with FOSAPREPITANT. This represents 4.3% of all adverse event reports for FOSAPREPITANT.
21
Reports of Intentional product use issue with FOSAPREPITANT
4.3%
of all FOSAPREPITANT reports
19
Deaths
21
Hospitalizations
How Dangerous Is Intentional product use issue From FOSAPREPITANT?
Of the 21 reports, 19 (90.5%) resulted in death, 21 (100.0%) required hospitalization, and 20 (95.2%) 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 FOSAPREPITANT. However, 21 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 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 FOSAPREPITANT Alternatives Have Lower Intentional product use issue Risk?
FOSAPREPITANT vs FOSAPREPITANT DIMEGLUMINE
FOSAPREPITANT vs FOSCARBIDOPA\FOSLEVODOPA
FOSAPREPITANT vs FOSCARNET
FOSAPREPITANT vs FOSFOMYCIN
FOSAPREPITANT vs FOSFOMYCIN TROMETHAMINE