Does TREPROSTINIL Cause Drug titration error? 219 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 219 reports of Drug titration error have been filed in association with TREPROSTINIL (TYVASO). This represents 0.2% of all adverse event reports for TREPROSTINIL.
219
Reports of Drug titration error with TREPROSTINIL
0.2%
of all TREPROSTINIL reports
8
Deaths
63
Hospitalizations
How Dangerous Is Drug titration error From TREPROSTINIL?
Of the 219 reports, 8 (3.7%) resulted in death, 63 (28.8%) required hospitalization, and 3 (1.4%) were considered life-threatening.
Is Drug titration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 219 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 Drug titration error?
GABAPENTIN (499)
BUPROPION\NALTREXONE (338)
SEMAGLUTIDE (131)
DROXIDOPA (84)
CENOBAMATE (81)
PROPRANOLOL (81)
LAMOTRIGINE (65)
SODIUM OXYBATE (63)
DEUTETRABENAZINE (48)
SIPONIMOD (47)
Which TREPROSTINIL Alternatives Have Lower Drug titration error Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE