Does GLUTAMINE Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with GLUTAMINE (Endari). This represents 0.2% of all adverse event reports for GLUTAMINE.
5
Reports of Product administration error with GLUTAMINE
0.2%
of all GLUTAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From GLUTAMINE?
Of the 5 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 5 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which GLUTAMINE Alternatives Have Lower Product administration error Risk?
GLUTAMINE vs GLUTATHIONE
GLUTAMINE vs GLYBURIDE
GLUTAMINE vs GLYBURIDE\METFORMIN
GLUTAMINE vs GLYCERIN
GLUTAMINE vs GLYCERIN\SORBITOL