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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 Extra dose administered? 251 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 251 reports of Extra dose administered have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.

251
Reports of Extra dose administered with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
5
Deaths
72
Hospitalizations

How Dangerous Is Extra dose administered From TREPROSTINIL?

Of the 251 reports, 5 (2.0%) resulted in death, 72 (28.7%) required hospitalization, and 3 (1.2%) were considered life-threatening.

Is Extra dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 251 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which TREPROSTINIL Alternatives Have Lower Extra dose administered 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 Extra dose administered Reports All Drugs Causing Extra dose administered TREPROSTINIL Demographics