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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 EPOPROSTENOL Cause Hypersensitivity? 156 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 156 reports of Hypersensitivity have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.2% of all adverse event reports for EPOPROSTENOL.

156
Reports of Hypersensitivity with EPOPROSTENOL
1.2%
of all EPOPROSTENOL reports
15
Deaths
120
Hospitalizations

How Dangerous Is Hypersensitivity From EPOPROSTENOL?

Of the 156 reports, 15 (9.6%) resulted in death, 120 (76.9%) required hospitalization, and 5 (3.2%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 156 reports have been filed with the FAERS database.

What Other Side Effects Does EPOPROSTENOL Cause?

Dyspnoea (2,744) Headache (2,425) Diarrhoea (2,310) Nausea (2,016) Pain in jaw (1,928) Death (1,362) Flushing (1,256) Fatigue (1,133) Hospitalisation (1,078) Vomiting (1,068)

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 EPOPROSTENOL Alternatives Have Lower Hypersensitivity Risk?

EPOPROSTENOL vs EPTIFIBATIDE EPOPROSTENOL vs EPTINEZUMAB-JJMR EPOPROSTENOL vs EPTINEZUMAB\EPTINEZUMAB-JJMR EPOPROSTENOL vs EQUINE BOTULINUM NEUROTOXIN A/B/C/D/E/F/G IMMUNE FAB2 EPOPROSTENOL vs EQUINE THYMOCYTE IMMUNE GLOBULIN

Related Pages

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