Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Glutamine
Drug ID BADD_D01029
Description A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from glutamic acid and ammonia. It is the principal carrier of nitrogen in the body and is an important energy source for many cells. An oral formulation of L-glutamine was approved by the FDA in July 2017 for use in sickle cell disease [L892]. This oral formulation is marketed under the tradename Endari by Emmaus Medical.
Indications and Usage Used for nutritional supplementation, also for treating dietary shortage or imbalance. Used to reduce the acute complications of sickle cell disease in adult and pediatric patients 5 years of age and older [FDA Label].
Marketing Status approved; investigational; nutraceutical
ATC Code A16AA03
DrugBank ID DB00130
KEGG ID D00015
MeSH ID D005973
PubChem ID 5961
TTD Drug ID D01JIA
NDC Product Code 58159-080; 42457-420; 51552-0285
UNII 0RH81L854J
Synonyms Glutamine | L-Glutamine | L Glutamine | D-Glutamine | D Glutamine
Chemical Information
Molecular Formula C5H10N2O3
CAS Registry Number 56-85-9
SMILES C(CC(=O)N)C(C(=O)O)N
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Headache17.14.01.001--
Hepatic function abnormal09.01.02.001--Not Available
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hypersensitivity10.01.03.003--
Infection11.01.08.002--Not Available
Influenza like illness08.01.03.010--
Injection site pain12.07.03.011; 08.02.03.010--Not Available
Injection site reaction12.07.03.015; 08.02.03.014--
Insomnia17.15.03.002; 19.02.01.002--
Laryngitis22.07.03.001; 11.01.13.001--
Malaise08.01.01.003--
Myalgia15.05.02.001--
Nail disorder23.02.05.002--
Nausea07.01.07.0010.014662%
Nephrolithiasis20.04.01.002--
Neuropathy peripheral17.09.03.003--Not Available
Oedema14.05.06.010; 08.01.07.006--Not Available
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Pain08.01.08.0040.011643%
Pancreatitis07.18.01.001--
Pharyngitis07.05.07.004; 22.07.03.004; 11.01.13.003--
Pneumonia streptococcal22.07.06.006; 11.02.06.005--Not Available
Proctalgia07.03.02.001--
Pruritus23.03.12.0010.009487%
Pyelonephritis20.01.09.001; 11.01.14.002--Not Available
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Rhinitis22.07.03.006; 11.01.13.004--
Sensory loss17.02.07.007--Not Available
Sepsis11.01.11.003--
The 2th Page    First    Pre   2 3    Next   Last    Total 3 Pages
ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene