Does TRIAZOLAM Cause Incorrect product administration duration? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product administration duration have been filed in association with TRIAZOLAM (Triazolam). This represents 0.4% of all adverse event reports for TRIAZOLAM.
7
Reports of Incorrect product administration duration with TRIAZOLAM
0.4%
of all TRIAZOLAM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From TRIAZOLAM?
Of the 7 reports, 1 (14.3%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIAZOLAM. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does TRIAZOLAM Cause?
Drug abuse (457)
Sopor (338)
Overdose (161)
Toxicity to various agents (161)
Intentional overdose (155)
Drug ineffective (149)
Intentional self-injury (136)
Completed suicide (118)
Suicide attempt (106)
Loss of consciousness (101)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TRIAZOLAM Alternatives Have Lower Incorrect product administration duration Risk?
TRIAZOLAM vs TRICHLORMETHIAZIDE
TRIAZOLAM vs TRICLOSAN
TRIAZOLAM vs TRIENTINE
TRIAZOLAM vs TRIENTINE TETRAHYDROCHLORIDE
TRIAZOLAM vs TRIFAROTENE