Does TREPROSTINIL Cause Incorrect drug administration rate? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Incorrect drug administration rate have been filed in association with TREPROSTINIL (TYVASO). This represents 0.2% of all adverse event reports for TREPROSTINIL.
149
Reports of Incorrect drug administration rate with TREPROSTINIL
0.2%
of all TREPROSTINIL reports
3
Deaths
50
Hospitalizations
How Dangerous Is Incorrect drug administration rate From TREPROSTINIL?
Of the 149 reports, 3 (2.0%) resulted in death, 50 (33.6%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Incorrect drug administration rate Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 149 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 Incorrect drug administration rate?
HUMAN IMMUNOGLOBULIN G (594)
INFLIXIMAB (344)
HUMAN IMMUNOGLOBULIN G\HYALURONIDASE (89)
NATALIZUMAB (74)
RITUXIMAB (74)
FLUOROURACIL (69)
VANCOMYCIN (60)
SODIUM (58)
INFLIXIMAB-ABDA (57)
BACLOFEN (51)
Which TREPROSTINIL Alternatives Have Lower Incorrect drug administration rate Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE