Does TREPROSTINIL Cause Device leakage? 874 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 874 reports of Device leakage have been filed in association with TREPROSTINIL (TYVASO). This represents 1.0% of all adverse event reports for TREPROSTINIL.
874
Reports of Device leakage with TREPROSTINIL
1.0%
of all TREPROSTINIL reports
26
Deaths
336
Hospitalizations
How Dangerous Is Device leakage From TREPROSTINIL?
Of the 874 reports, 26 (3.0%) resulted in death, 336 (38.4%) required hospitalization, and 15 (1.7%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 874 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which TREPROSTINIL Alternatives Have Lower Device leakage Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE