Does GLUTAMINE Cause Wrong technique in product usage process? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong technique in product usage process have been filed in association with GLUTAMINE (Endari). This represents 0.2% of all adverse event reports for GLUTAMINE.
6
Reports of Wrong technique in product usage process with GLUTAMINE
0.2%
of all GLUTAMINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From GLUTAMINE?
Of the 6 reports, 1 (16.7%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLUTAMINE. However, 6 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which GLUTAMINE Alternatives Have Lower Wrong technique in product usage process Risk?
GLUTAMINE vs GLUTATHIONE
GLUTAMINE vs GLYBURIDE
GLUTAMINE vs GLYBURIDE\METFORMIN
GLUTAMINE vs GLYCERIN
GLUTAMINE vs GLYCERIN\SORBITOL