Does EPOPROSTENOL Cause Device dislocation? 358 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 358 reports of Device dislocation have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 2.7% of all adverse event reports for EPOPROSTENOL.
358
Reports of Device dislocation with EPOPROSTENOL
2.7%
of all EPOPROSTENOL reports
48
Deaths
315
Hospitalizations
How Dangerous Is Device dislocation From EPOPROSTENOL?
Of the 358 reports, 48 (13.4%) resulted in death, 315 (88.0%) required hospitalization, and 7 (2.0%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 358 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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
DEXAMETHASONE (290)
Which EPOPROSTENOL Alternatives Have Lower Device dislocation 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