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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 APREPITANT Cause Duodenal ulcer perforation? 650 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 650 reports of Duodenal ulcer perforation have been filed in association with APREPITANT (CINVANTI). This represents 11.6% of all adverse event reports for APREPITANT.

650
Reports of Duodenal ulcer perforation with APREPITANT
11.6%
of all APREPITANT reports
330
Deaths
581
Hospitalizations

How Dangerous Is Duodenal ulcer perforation From APREPITANT?

Of the 650 reports, 330 (50.8%) resulted in death, 581 (89.4%) required hospitalization, and 378 (58.2%) were considered life-threatening.

Is Duodenal ulcer perforation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APREPITANT. However, 650 reports have been filed with the FAERS database.

What Other Side Effects Does APREPITANT Cause?

Fatigue (955) Pyrexia (913) Dyspnoea (909) Hypersensitivity (881) Rash (789) Alopecia (760) Gastrointestinal disorder (722) Pruritus (707) Confusional state (696) Glossodynia (696)

What Other Drugs Cause Duodenal ulcer perforation?

METHOTREXATE (4,239) LEFLUNOMIDE (4,200) FOLIC ACID (4,152) ABATACEPT (4,147) TOCILIZUMAB (4,130) DICLOFENAC (4,120) CETIRIZINE (4,117) DESOXIMETASONE (4,084) RITUXIMAB (4,081) PREDNISONE (4,060)

Which APREPITANT Alternatives Have Lower Duodenal ulcer perforation Risk?

APREPITANT vs APROTININ APREPITANT vs ARANESP APREPITANT vs ARAVA APREPITANT vs AREDIA APREPITANT vs ARFORMOTEROL

Related Pages

APREPITANT Full Profile All Duodenal ulcer perforation Reports All Drugs Causing Duodenal ulcer perforation APREPITANT Demographics