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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 Incorrect dose administered? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Incorrect dose administered have been filed in association with GLUTAMINE (Endari). This represents 0.7% of all adverse event reports for GLUTAMINE.

23
Reports of Incorrect dose administered with GLUTAMINE
0.7%
of all GLUTAMINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Incorrect dose administered From GLUTAMINE?

Of the 23 reports, 5 (21.7%) required hospitalization.

Is Incorrect dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 23 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 Incorrect dose administered?

TIRZEPATIDE (23,301) ADALIMUMAB (14,000) DUPILUMAB (9,907) RANITIDINE (9,337) INSULIN LISPRO (8,318) ACETAMINOPHEN (5,316) DULAGLUTIDE (5,207) SECUKINUMAB (4,524) INSULIN GLARGINE (3,070) SOMATROPIN (2,772)

Which GLUTAMINE Alternatives Have Lower Incorrect dose administered Risk?

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

Related Pages

GLUTAMINE Full Profile All Incorrect dose administered Reports All Drugs Causing Incorrect dose administered GLUTAMINE Demographics