Does EPOPROSTENOL Cause Application site pruritus? 87 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 87 reports of Application site pruritus have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.7% of all adverse event reports for EPOPROSTENOL.
87
Reports of Application site pruritus with EPOPROSTENOL
0.7%
of all EPOPROSTENOL reports
15
Deaths
62
Hospitalizations
How Dangerous Is Application site pruritus From EPOPROSTENOL?
Of the 87 reports, 15 (17.2%) resulted in death, 62 (71.3%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Application site pruritus Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 87 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 Application site pruritus?
MINOXIDIL (3,727)
NICOTINE (2,074)
BUPRENORPHINE (1,687)
ESTRADIOL (1,181)
SUMATRIPTAN (675)
FENTANYL (501)
ESTRADIOL\NORETHINDRONE (463)
CLONIDINE (335)
ROTIGOTINE (334)
INGENOL MEBUTATE (291)
Which EPOPROSTENOL Alternatives Have Lower Application site pruritus 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