Does TREPROSTINIL Cause Wrong technique in product usage process? 412 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 412 reports of Wrong technique in product usage process have been filed in association with TREPROSTINIL (TYVASO). This represents 0.5% of all adverse event reports for TREPROSTINIL.
412
Reports of Wrong technique in product usage process with TREPROSTINIL
0.5%
of all TREPROSTINIL reports
12
Deaths
94
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TREPROSTINIL?
Of the 412 reports, 12 (2.9%) resulted in death, 94 (22.8%) required hospitalization, and 9 (2.2%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 412 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which TREPROSTINIL Alternatives Have Lower Wrong technique in product usage process Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE