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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 Physical deconditioning? 33 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Physical deconditioning have been filed in association with TREPROSTINIL (TYVASO). This represents 0.0% of all adverse event reports for TREPROSTINIL.

33
Reports of Physical deconditioning with TREPROSTINIL
0.0%
of all TREPROSTINIL reports
8
Deaths
23
Hospitalizations

How Dangerous Is Physical deconditioning From TREPROSTINIL?

Of the 33 reports, 8 (24.2%) resulted in death, 23 (69.7%) required hospitalization, and 2 (6.1%) were considered life-threatening.

Is Physical deconditioning Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 33 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 Physical deconditioning?

ACETAMINOPHEN (193) ESOMEPRAZOLE (189) AMLODIPINE (186) FLUOXETINE (184) TOFACITINIB (182) ESCITALOPRAM OXALATE (181) MOCLOBEMIDE (178) VALSARTAN (176) VENLAFAXINE (176) TRAMADOL (173)

Which TREPROSTINIL Alternatives Have Lower Physical deconditioning 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 Physical deconditioning Reports All Drugs Causing Physical deconditioning TREPROSTINIL Demographics