Does TREPROSTINIL Cause Product physical issue? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Product physical issue have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.
90
Reports of Product physical issue with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
1
Deaths
16
Hospitalizations
How Dangerous Is Product physical issue From TREPROSTINIL?
Of the 90 reports, 1 (1.1%) resulted in death, 16 (17.8%) required hospitalization.
Is Product physical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 90 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 physical issue?
SUMATRIPTAN (2,349)
TIOTROPIUM (807)
ICOSAPENT ETHYL (666)
LISDEXAMFETAMINE DIMESYLATE (652)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (387)
IBUPROFEN (337)
ESTRADIOL\LEVONORGESTREL (305)
ESTRADIOL (302)
RUXOLITINIB (302)
IXAZOMIB (298)
Which TREPROSTINIL Alternatives Have Lower Product physical issue Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE