Does TREPROSTINIL Cause Product leakage? 213 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 213 reports of Product leakage have been filed in association with TREPROSTINIL (TYVASO). This represents 0.2% of all adverse event reports for TREPROSTINIL.
213
Reports of Product leakage with TREPROSTINIL
0.2%
of all TREPROSTINIL reports
5
Deaths
62
Hospitalizations
How Dangerous Is Product leakage From TREPROSTINIL?
Of the 213 reports, 5 (2.3%) resulted in death, 62 (29.1%) required hospitalization, and 3 (1.4%) were considered life-threatening.
Is Product leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 213 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 Product leakage?
GUSELKUMAB (661)
INSULIN ASPART (361)
USTEKINUMAB (344)
LEUPROLIDE (331)
SUMATRIPTAN (275)
ABATACEPT (124)
SECUKINUMAB (116)
PALIPERIDONE (92)
ICOSAPENT ETHYL (80)
GOLIMUMAB (79)
Which TREPROSTINIL Alternatives Have Lower Product leakage Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE