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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 GLUTATHIONE Cause Off label use? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Off label use have been filed in association with GLUTATHIONE (Dark Spot Corrector Serum). This represents 4.7% of all adverse event reports for GLUTATHIONE.

7
Reports of Off label use with GLUTATHIONE
4.7%
of all GLUTATHIONE reports
1
Deaths
4
Hospitalizations

How Dangerous Is Off label use From GLUTATHIONE?

Of the 7 reports, 1 (14.3%) resulted in death, 4 (57.1%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLUTATHIONE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does GLUTATHIONE Cause?

Condition aggravated (26) Dyspnoea (24) Pain (22) Drug ineffective (20) Chest pain (19) Malaise (19) Cough (17) Seizure (17) Stomatitis (17) Eczema (16)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Which GLUTATHIONE Alternatives Have Lower Off label use Risk?

GLUTATHIONE vs GLYBURIDE GLUTATHIONE vs GLYBURIDE\METFORMIN GLUTATHIONE vs GLYCERIN GLUTATHIONE vs GLYCERIN\SORBITOL GLUTATHIONE vs GLYCEROL PHENYLBUTYRATE

Related Pages

GLUTATHIONE Full Profile All Off label use Reports All Drugs Causing Off label use GLUTATHIONE Demographics