Does TRIENTINE Cause Wrong technique in product usage process? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong technique in product usage process have been filed in association with TRIENTINE (Trientine Hydrochloride). This represents 2.3% of all adverse event reports for TRIENTINE.
5
Reports of Wrong technique in product usage process with TRIENTINE
2.3%
of all TRIENTINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TRIENTINE?
Of the 5 reports, 2 (40.0%) required hospitalization.
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 TRIENTINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does TRIENTINE Cause?
Drug dose omission (20)
Therapy interrupted (16)
Drug ineffective (15)
Product storage error (15)
Treatment noncompliance (14)
Fatigue (12)
Nausea (12)
Death (11)
Insurance issue (11)
Hepatic failure (10)
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 TRIENTINE Alternatives Have Lower Wrong technique in product usage process Risk?
TRIENTINE vs TRIENTINE TETRAHYDROCHLORIDE
TRIENTINE vs TRIFAROTENE
TRIENTINE vs TRIFLUOPERAZINE
TRIENTINE vs TRIFLURIDINE
TRIENTINE vs TRIHEPTANOIN