Does GLUTAMINE Cause Product dose omission? 268 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 268 reports of Product dose omission have been filed in association with GLUTAMINE (Endari). This represents 8.0% of all adverse event reports for GLUTAMINE.
268
Reports of Product dose omission with GLUTAMINE
8.0%
of all GLUTAMINE reports
0
Deaths
85
Hospitalizations
How Dangerous Is Product dose omission From GLUTAMINE?
Of the 268 reports, 85 (31.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 268 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)
Pain (207)
Hospitalisation (176)
Nausea (144)
Headache (129)
Abdominal pain upper (121)
Drug dose omission (118)
Constipation (117)
Pain in extremity (104)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which GLUTAMINE Alternatives Have Lower Product dose omission Risk?
GLUTAMINE vs GLUTATHIONE
GLUTAMINE vs GLYBURIDE
GLUTAMINE vs GLYBURIDE\METFORMIN
GLUTAMINE vs GLYCERIN
GLUTAMINE vs GLYCERIN\SORBITOL