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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 Haemoptysis? 220 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 220 reports of Haemoptysis have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.7% of all adverse event reports for EPOPROSTENOL.

220
Reports of Haemoptysis with EPOPROSTENOL
1.7%
of all EPOPROSTENOL reports
68
Deaths
191
Hospitalizations

How Dangerous Is Haemoptysis From EPOPROSTENOL?

Of the 220 reports, 68 (30.9%) resulted in death, 191 (86.8%) required hospitalization, and 23 (10.5%) were considered life-threatening.

Is Haemoptysis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 220 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 Haemoptysis?

RIVAROXABAN (1,961) ASPIRIN (1,255) APIXABAN (846) TREPROSTINIL (838) ALBUTEROL (652) CLOPIDOGREL BISULFATE (643) PREDNISONE (618) WARFARIN (555) ADALIMUMAB (472) TIOTROPIUM (462)

Which EPOPROSTENOL Alternatives Have Lower Haemoptysis 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 Haemoptysis Reports All Drugs Causing Haemoptysis EPOPROSTENOL Demographics