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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 Therapy interrupted? 44 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Therapy interrupted have been filed in association with GLUTAMINE (Endari). This represents 1.3% of all adverse event reports for GLUTAMINE.

44
Reports of Therapy interrupted with GLUTAMINE
1.3%
of all GLUTAMINE reports
0
Deaths
18
Hospitalizations

How Dangerous Is Therapy interrupted From GLUTAMINE?

Of the 44 reports, 18 (40.9%) required hospitalization.

Is Therapy interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 44 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 Therapy interrupted?

ADALIMUMAB (5,755) ETANERCEPT (3,397) RELUGOLIX (3,251) CERTOLIZUMAB PEGOL (3,209) LENALIDOMIDE (2,724) UPADACITINIB (1,741) ABATACEPT (1,726) CLOZAPINE (1,722) AMIKACIN (1,283) TOFACITINIB (1,182)

Which GLUTAMINE Alternatives Have Lower Therapy interrupted Risk?

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

Related Pages

GLUTAMINE Full Profile All Therapy interrupted Reports All Drugs Causing Therapy interrupted GLUTAMINE Demographics