Does THIAMINE Cause Incorrect product administration duration? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Incorrect product administration duration have been filed in association with THIAMINE (Thiamine Hydrochloride). This represents 1.2% of all adverse event reports for THIAMINE.
20
Reports of Incorrect product administration duration with THIAMINE
1.2%
of all THIAMINE reports
20
Deaths
20
Hospitalizations
How Dangerous Is Incorrect product administration duration From THIAMINE?
Of the 20 reports, 20 (100.0%) resulted in death, 20 (100.0%) required hospitalization, and 20 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for THIAMINE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does THIAMINE Cause?
Off label use (423)
Drug ineffective (375)
Pain (274)
Condition aggravated (249)
Drug hypersensitivity (233)
Product use in unapproved indication (229)
Drug intolerance (216)
Infusion related reaction (207)
Nausea (207)
Dyspnoea (200)
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 THIAMINE Alternatives Have Lower Incorrect product administration duration Risk?
THIAMINE vs THIOCOLCHICOSIDE
THIAMINE vs THIOGUANINE
THIAMINE vs THIOGUANINE ANHYDROUS
THIAMINE vs THIOPENTAL
THIAMINE vs THIORIDAZINE