Does TREPROSTINIL Cause Device malfunction? 924 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 924 reports of Device malfunction have been filed in association with TREPROSTINIL (TYVASO). This represents 1.0% of all adverse event reports for TREPROSTINIL.
924
Reports of Device malfunction with TREPROSTINIL
1.0%
of all TREPROSTINIL reports
24
Deaths
315
Hospitalizations
How Dangerous Is Device malfunction From TREPROSTINIL?
Of the 924 reports, 24 (2.6%) resulted in death, 315 (34.1%) required hospitalization, and 30 (3.2%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 924 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which TREPROSTINIL Alternatives Have Lower Device malfunction Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE