Does TREPROSTINIL Cause Device power source issue? 299 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 299 reports of Device power source issue have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.
299
Reports of Device power source issue with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
4
Deaths
83
Hospitalizations
How Dangerous Is Device power source issue From TREPROSTINIL?
Of the 299 reports, 4 (1.3%) resulted in death, 83 (27.8%) required hospitalization, and 2 (0.7%) were considered life-threatening.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 299 reports have been filed with the FAERS database.
What Other Side Effects Does TREPROSTINIL Cause?
Dyspnoea (16,348)
Headache (14,051)
Diarrhoea (11,335)
Nausea (10,320)
Cough (8,945)
Fatigue (7,440)
Dizziness (7,405)
Infusion site pain (5,169)
Vomiting (5,097)
Death (4,764)
What Other Drugs Cause Device power source issue?
SOMATROPIN (1,219)
PEGFILGRASTIM (486)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
DEVICE (20)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which TREPROSTINIL Alternatives Have Lower Device power source issue Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE