The most commonly reported side effects of l include sickle cell anaemia with crisis, product dose omission issue, and pain, based on 4,923 FDA adverse event reports from 2004 to 2025. 2.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for l.
These are voluntary reports and do not establish that l caused these reactions.
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Other drugs that appear in adverse event reports alongside l. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
57.1% of l adverse event reports involve female patients and 40.1% involve male patients. The largest age group is adult at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking l when the adverse event was reported.
Showing 15 of 146 indications
L is sold under the brand name L-glutamine.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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