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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 Hyperkalaemia? 61 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Hyperkalaemia have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.

61
Reports of Hyperkalaemia with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
15
Deaths
54
Hospitalizations

How Dangerous Is Hyperkalaemia From TREPROSTINIL?

Of the 61 reports, 15 (24.6%) resulted in death, 54 (88.5%) required hospitalization, and 5 (8.2%) were considered life-threatening.

Is Hyperkalaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 61 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 Hyperkalaemia?

METFORMIN (2,565) SPIRONOLACTONE (2,518) FUROSEMIDE (2,035) RAMIPRIL (1,383) SACUBITRIL\VALSARTAN (1,192) SULFAMETHOXAZOLE\TRIMETHOPRIM (1,036) LISINOPRIL (948) POTASSIUM (944) BISOPROLOL (850) TACROLIMUS (713)

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