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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 GLUTAMINE Cause Off label use? 60 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Off label use have been filed in association with GLUTAMINE (Endari). This represents 1.8% of all adverse event reports for GLUTAMINE.

60
Reports of Off label use with GLUTAMINE
1.8%
of all GLUTAMINE reports
2
Deaths
20
Hospitalizations

How Dangerous Is Off label use From GLUTAMINE?

Of the 60 reports, 2 (3.3%) resulted in death, 20 (33.3%) required hospitalization, and 1 (1.7%) 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 GLUTAMINE. However, 60 reports have been filed with the FAERS database.

What Other Side Effects Does GLUTAMINE Cause?

Sickle cell anaemia with crisis (1,482) Product dose omission issue (590) Product dose omission (268) Pain (207) Hospitalisation (176) Nausea (144) Headache (129) Abdominal pain upper (121) Drug dose omission (118) Constipation (117)

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 GLUTAMINE Alternatives Have Lower Off label use Risk?

GLUTAMINE vs GLUTATHIONE GLUTAMINE vs GLYBURIDE GLUTAMINE vs GLYBURIDE\METFORMIN GLUTAMINE vs GLYCERIN GLUTAMINE vs GLYCERIN\SORBITOL

Related Pages

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