Does GLUTAMINE Cause Product use complaint? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product use complaint have been filed in association with GLUTAMINE (Endari). This represents 0.3% of all adverse event reports for GLUTAMINE.
11
Reports of Product use complaint with GLUTAMINE
0.3%
of all GLUTAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use complaint From GLUTAMINE?
Of the 11 reports.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 11 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 Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which GLUTAMINE Alternatives Have Lower Product use complaint Risk?
GLUTAMINE vs GLUTATHIONE
GLUTAMINE vs GLYBURIDE
GLUTAMINE vs GLYBURIDE\METFORMIN
GLUTAMINE vs GLYCERIN
GLUTAMINE vs GLYCERIN\SORBITOL