Does EPOPROSTENOL Cause Unevaluable event? 234 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 234 reports of Unevaluable event have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.8% of all adverse event reports for EPOPROSTENOL.
234
Reports of Unevaluable event with EPOPROSTENOL
1.8%
of all EPOPROSTENOL reports
46
Deaths
205
Hospitalizations
How Dangerous Is Unevaluable event From EPOPROSTENOL?
Of the 234 reports, 46 (19.7%) resulted in death, 205 (87.6%) required hospitalization, and 3 (1.3%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 234 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which EPOPROSTENOL Alternatives Have Lower Unevaluable event 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