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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 Condition aggravated? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with RIBOFLAVIN\THIAMINE. This represents 19.2% of all adverse event reports for RIBOFLAVIN\THIAMINE.

5
Reports of Condition aggravated with RIBOFLAVIN\THIAMINE
19.2%
of all RIBOFLAVIN\THIAMINE reports
5
Deaths
5
Hospitalizations

How Dangerous Is Condition aggravated From RIBOFLAVIN\THIAMINE?

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

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIBOFLAVIN\THIAMINE. However, 5 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Related Pages

RIBOFLAVIN\THIAMINE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated RIBOFLAVIN\THIAMINE Demographics