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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 Ocular hyperaemia? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Ocular hyperaemia have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.2% of all adverse event reports for EPOPROSTENOL.

31
Reports of Ocular hyperaemia with EPOPROSTENOL
0.2%
of all EPOPROSTENOL reports
8
Deaths
21
Hospitalizations

How Dangerous Is Ocular hyperaemia From EPOPROSTENOL?

Of the 31 reports, 8 (25.8%) resulted in death, 21 (67.7%) required hospitalization.

Is Ocular hyperaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 31 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 Ocular hyperaemia?

DUPILUMAB (6,938) CYCLOSPORINE (1,508) BIMATOPROST (1,447) CENEGERMIN-BKBJ (1,226) BRIMONIDINE (917) ADALIMUMAB (714) LATANOPROST (587) DORZOLAMIDE\TIMOLOL (581) LIFITEGRAST (570) TRAVOPROST (478)

Which EPOPROSTENOL Alternatives Have Lower Ocular hyperaemia 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 Ocular hyperaemia Reports All Drugs Causing Ocular hyperaemia EPOPROSTENOL Demographics