Does TREPROSTINIL Cause Drug dose omission? 1,900 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,900 reports of Drug dose omission have been filed in association with TREPROSTINIL (TYVASO). This represents 2.1% of all adverse event reports for TREPROSTINIL.
1,900
Reports of Drug dose omission with TREPROSTINIL
2.1%
of all TREPROSTINIL reports
60
Deaths
667
Hospitalizations
How Dangerous Is Drug dose omission From TREPROSTINIL?
Of the 1,900 reports, 60 (3.2%) resulted in death, 667 (35.1%) required hospitalization, and 11 (0.6%) were considered life-threatening.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 1,900 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 Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which TREPROSTINIL Alternatives Have Lower Drug dose omission Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE