Does TREPROSTINIL Cause Product use complaint? 128 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 128 reports of Product use complaint have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.
128
Reports of Product use complaint with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
7
Deaths
28
Hospitalizations
How Dangerous Is Product use complaint From TREPROSTINIL?
Of the 128 reports, 7 (5.5%) resulted in death, 28 (21.9%) required hospitalization, and 2 (1.6%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 128 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which TREPROSTINIL Alternatives Have Lower Product use complaint Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE