Does GLUTAMINE Cause Product dose omission issue? 590 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 590 reports of Product dose omission issue have been filed in association with GLUTAMINE (Endari). This represents 17.7% of all adverse event reports for GLUTAMINE.
590
Reports of Product dose omission issue with GLUTAMINE
17.7%
of all GLUTAMINE reports
0
Deaths
244
Hospitalizations
How Dangerous Is Product dose omission issue From GLUTAMINE?
Of the 590 reports, 244 (41.4%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 590 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 (268)
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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which GLUTAMINE Alternatives Have Lower Product dose omission issue Risk?
GLUTAMINE vs GLUTATHIONE
GLUTAMINE vs GLYBURIDE
GLUTAMINE vs GLYBURIDE\METFORMIN
GLUTAMINE vs GLYCERIN
GLUTAMINE vs GLYCERIN\SORBITOL