Does EPOPROSTENOL Cause Device related sepsis? 89 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 89 reports of Device related sepsis have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.7% of all adverse event reports for EPOPROSTENOL.
89
Reports of Device related sepsis with EPOPROSTENOL
0.7%
of all EPOPROSTENOL reports
20
Deaths
86
Hospitalizations
How Dangerous Is Device related sepsis From EPOPROSTENOL?
Of the 89 reports, 20 (22.5%) resulted in death, 86 (96.6%) required hospitalization, and 5 (5.6%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 89 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 related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
ADALIMUMAB (49)
Which EPOPROSTENOL Alternatives Have Lower Device related sepsis 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