Does EPOPROSTENOL Cause Device issue? 201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Device issue have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.5% of all adverse event reports for EPOPROSTENOL.
201
Reports of Device issue with EPOPROSTENOL
1.5%
of all EPOPROSTENOL reports
34
Deaths
160
Hospitalizations
How Dangerous Is Device issue From EPOPROSTENOL?
Of the 201 reports, 34 (16.9%) resulted in death, 160 (79.6%) required hospitalization, and 12 (6.0%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 201 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which EPOPROSTENOL Alternatives Have Lower Device issue 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