Does TREPROSTINIL Cause Device failure? 713 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 713 reports of Device failure have been filed in association with TREPROSTINIL (TYVASO). This represents 0.8% of all adverse event reports for TREPROSTINIL.
713
Reports of Device failure with TREPROSTINIL
0.8%
of all TREPROSTINIL reports
14
Deaths
197
Hospitalizations
How Dangerous Is Device failure From TREPROSTINIL?
Of the 713 reports, 14 (2.0%) resulted in death, 197 (27.6%) required hospitalization, and 9 (1.3%) were considered life-threatening.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 713 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 failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
INSULIN ASPART (271)
Which TREPROSTINIL Alternatives Have Lower Device failure Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE