Does EPOPROSTENOL Cause Device breakage? 240 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 240 reports of Device breakage have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.8% of all adverse event reports for EPOPROSTENOL.
240
Reports of Device breakage with EPOPROSTENOL
1.8%
of all EPOPROSTENOL reports
39
Deaths
214
Hospitalizations
How Dangerous Is Device breakage From EPOPROSTENOL?
Of the 240 reports, 39 (16.3%) resulted in death, 214 (89.2%) required hospitalization, and 14 (5.8%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 240 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
INSULIN GLARGINE (237)
Which EPOPROSTENOL Alternatives Have Lower Device breakage 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