Does EPOPROSTENOL Cause Device malfunction? 228 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 228 reports of Device malfunction have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.7% of all adverse event reports for EPOPROSTENOL.
228
Reports of Device malfunction with EPOPROSTENOL
1.7%
of all EPOPROSTENOL reports
42
Deaths
197
Hospitalizations
How Dangerous Is Device malfunction From EPOPROSTENOL?
Of the 228 reports, 42 (18.4%) resulted in death, 197 (86.4%) required hospitalization, and 15 (6.6%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 228 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 Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which EPOPROSTENOL Alternatives Have Lower Device malfunction 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