Does THIAMINE Cause Product use in unapproved indication? 229 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 229 reports of Product use in unapproved indication have been filed in association with THIAMINE (Thiamine Hydrochloride). This represents 13.2% of all adverse event reports for THIAMINE.
229
Reports of Product use in unapproved indication with THIAMINE
13.2%
of all THIAMINE reports
155
Deaths
171
Hospitalizations
How Dangerous Is Product use in unapproved indication From THIAMINE?
Of the 229 reports, 155 (67.7%) resulted in death, 171 (74.7%) required hospitalization, and 151 (65.9%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for THIAMINE. However, 229 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)
Drug intolerance (216)
Infusion related reaction (207)
Nausea (207)
Dyspnoea (200)
Gastrooesophageal reflux disease (200)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which THIAMINE Alternatives Have Lower Product use in unapproved indication Risk?
THIAMINE vs THIOCOLCHICOSIDE
THIAMINE vs THIOGUANINE
THIAMINE vs THIOGUANINE ANHYDROUS
THIAMINE vs THIOPENTAL
THIAMINE vs THIORIDAZINE