Does RIBOFLAVIN 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 RIBOFLAVIN. This represents 2.4% of all adverse event reports for RIBOFLAVIN.
20
Reports of Incorrect product administration duration with RIBOFLAVIN
2.4%
of all RIBOFLAVIN reports
20
Deaths
20
Hospitalizations
How Dangerous Is Incorrect product administration duration From RIBOFLAVIN?
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 RIBOFLAVIN. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does RIBOFLAVIN Cause?
Off label use (410)
Drug ineffective (372)
Nausea (271)
Drug hypersensitivity (270)
Product use in unapproved indication (265)
Pain (264)
Infusion related reaction (225)
Swelling (223)
Sleep disorder (214)
Pericarditis (210)
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 RIBOFLAVIN Alternatives Have Lower Incorrect product administration duration Risk?
RIBOFLAVIN vs RIBOFLAVIN 5'-PHOSPHATE
RIBOFLAVIN vs RIBOFLAVIN 5^-PHOSPHATE
RIBOFLAVIN vs RIFABUTIN
RIBOFLAVIN vs RIFAMPICIN
RIBOFLAVIN vs RIFAMPIN