Does TREPROSTINIL Cause Application site pruritus? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Application site pruritus have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.
49
Reports of Application site pruritus with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
4
Deaths
28
Hospitalizations
How Dangerous Is Application site pruritus From TREPROSTINIL?
Of the 49 reports, 4 (8.2%) resulted in death, 28 (57.1%) required hospitalization, and 1 (2.0%) were considered life-threatening.
Is Application site pruritus Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 49 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 Application site pruritus?
MINOXIDIL (3,727)
NICOTINE (2,074)
BUPRENORPHINE (1,687)
ESTRADIOL (1,181)
SUMATRIPTAN (675)
FENTANYL (501)
ESTRADIOL\NORETHINDRONE (463)
CLONIDINE (335)
ROTIGOTINE (334)
INGENOL MEBUTATE (291)
Which TREPROSTINIL Alternatives Have Lower Application site pruritus Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE