Does TREPROSTINIL Cause Cardioactive drug level increased? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Cardioactive drug level increased have been filed in association with TREPROSTINIL (TYVASO). This represents 0.0% of all adverse event reports for TREPROSTINIL.
8
Reports of Cardioactive drug level increased with TREPROSTINIL
0.0%
of all TREPROSTINIL reports
2
Deaths
8
Hospitalizations
How Dangerous Is Cardioactive drug level increased From TREPROSTINIL?
Of the 8 reports, 2 (25.0%) resulted in death, 8 (100.0%) required hospitalization, and 2 (25.0%) were considered life-threatening.
Is Cardioactive drug level increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 8 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 Cardioactive drug level increased?
DIGOXIN (325)
FUROSEMIDE (92)
BISOPROLOL (45)
CLARITHROMYCIN (34)
AMIODARONE (31)
SPIRONOLACTONE (25)
CARVEDILOL (22)
WARFARIN (21)
LANSOPRAZOLE (16)
METFORMIN (16)
Which TREPROSTINIL Alternatives Have Lower Cardioactive drug level increased Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE