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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 Presyncope? 585 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 585 reports of Presyncope have been filed in association with TREPROSTINIL (TYVASO). This represents 0.6% of all adverse event reports for TREPROSTINIL.

585
Reports of Presyncope with TREPROSTINIL
0.6%
of all TREPROSTINIL reports
29
Deaths
268
Hospitalizations

How Dangerous Is Presyncope From TREPROSTINIL?

Of the 585 reports, 29 (5.0%) resulted in death, 268 (45.8%) required hospitalization, and 5 (0.9%) were considered life-threatening.

Is Presyncope Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 585 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 Presyncope?

BISOPROLOL (485) LEVONORGESTREL (429) ADALIMUMAB (420) AMBRISENTAN (407) ASPIRIN (370) TAMSULOSIN (361) FUROSEMIDE (348) SERTRALINE (337) ETANERCEPT (334) RAMIPRIL (332)

Which TREPROSTINIL Alternatives Have Lower Presyncope 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 Presyncope Reports All Drugs Causing Presyncope TREPROSTINIL Demographics