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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TREPROSTINIL Cause Dysgeusia? 288 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 288 reports of Dysgeusia have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.

288
Reports of Dysgeusia with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
11
Deaths
68
Hospitalizations

How Dangerous Is Dysgeusia From TREPROSTINIL?

Of the 288 reports, 11 (3.8%) resulted in death, 68 (23.6%) required hospitalization, and 2 (0.7%) were considered life-threatening.

Is Dysgeusia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 288 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 Dysgeusia?

NIRMATRELVIR\RITONAVIR (7,381) SUNITINIB MALATE (1,226) SODIUM (1,216) LENALIDOMIDE (1,180) LIFITEGRAST (1,067) CABOZANTINIB S-MALATE (777) CLARITHROMYCIN (717) VISMODEGIB (706) ADALIMUMAB (674) PALBOCICLIB (620)

Which TREPROSTINIL Alternatives Have Lower Dysgeusia Risk?

TREPROSTINIL vs TREPROSTINIL DIOLAMINE TREPROSTINIL vs TRETINOIN TREPROSTINIL vs TRIAMCINOLONE TREPROSTINIL vs TRIAMCINOLONE ACETONIDE TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE

Related Pages

TREPROSTINIL Full Profile All Dysgeusia Reports All Drugs Causing Dysgeusia TREPROSTINIL Demographics