Does TREPROSTINIL Cause Complication of device removal? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Complication of device removal have been filed in association with TREPROSTINIL (TYVASO). This represents 0.0% of all adverse event reports for TREPROSTINIL.
24
Reports of Complication of device removal with TREPROSTINIL
0.0%
of all TREPROSTINIL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Complication of device removal From TREPROSTINIL?
Of the 24 reports, 4 (16.7%) required hospitalization.
Is Complication of device removal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 24 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 Complication of device removal?
COPPER (7,895)
ETONOGESTREL (3,578)
LEVONORGESTREL (2,039)
MIRENA (44)
INTERFERON BETA-1A (37)
IMPLANON (21)
ETHINYL ESTRADIOL\ETONOGESTREL (15)
UNSPECIFIED INGREDIENT (14)
BUPRENORPHINE (11)
DEVICE (11)
Which TREPROSTINIL Alternatives Have Lower Complication of device removal Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE