Does EPOPROSTENOL Cause Device leakage? 407 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 407 reports of Device leakage have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 3.1% of all adverse event reports for EPOPROSTENOL.
407
Reports of Device leakage with EPOPROSTENOL
3.1%
of all EPOPROSTENOL reports
54
Deaths
332
Hospitalizations
How Dangerous Is Device leakage From EPOPROSTENOL?
Of the 407 reports, 54 (13.3%) resulted in death, 332 (81.6%) required hospitalization, and 18 (4.4%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 407 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which EPOPROSTENOL Alternatives Have Lower Device leakage 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