Does EPOPROSTENOL Cause Complication associated with device? 399 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 399 reports of Complication associated with device have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 3.0% of all adverse event reports for EPOPROSTENOL.
399
Reports of Complication associated with device with EPOPROSTENOL
3.0%
of all EPOPROSTENOL reports
47
Deaths
322
Hospitalizations
How Dangerous Is Complication associated with device From EPOPROSTENOL?
Of the 399 reports, 47 (11.8%) resulted in death, 322 (80.7%) required hospitalization, and 17 (4.3%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 399 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
AMBRISENTAN (125)
Which EPOPROSTENOL Alternatives Have Lower Complication associated with device 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