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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 Adverse event? 82 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 82 reports of Adverse event have been filed in association with GLUTAMINE (Endari). This represents 2.5% of all adverse event reports for GLUTAMINE.

82
Reports of Adverse event with GLUTAMINE
2.5%
of all GLUTAMINE reports
0
Deaths
68
Hospitalizations

How Dangerous Is Adverse event From GLUTAMINE?

Of the 82 reports, 68 (82.9%) required hospitalization.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 82 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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which GLUTAMINE Alternatives Have Lower