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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RIBOFLAVIN\THIAMINE Cause Product use issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use issue have been filed in association with RIBOFLAVIN\THIAMINE. This represents 23.1% of all adverse event reports for RIBOFLAVIN\THIAMINE.

6
Reports of Product use issue with RIBOFLAVIN\THIAMINE
23.1%
of all RIBOFLAVIN\THIAMINE reports
6
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From RIBOFLAVIN\THIAMINE?

Of the 6 reports, 6 (100.0%) resulted in death, 5 (83.3%) required hospitalization, and 5 (83.3%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIBOFLAVIN\THIAMINE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does RIBOFLAVIN\THIAMINE Cause?

Gastrooesophageal reflux disease (26) Blepharospasm (25) Epilepsy (25) Hypoaesthesia (25) Paraesthesia (25) Vomiting (25) Abdominal pain upper (24) Drug intolerance (24) Memory impairment (24) Taste disorder (24)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

RIBOFLAVIN\THIAMINE Full Profile All Product use issue Reports All Drugs Causing Product use issue RIBOFLAVIN\THIAMINE Demographics