Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Memantine
Drug ID BADD_D01378
Description Initially approved by the FDA in 2013, memantine is an N-methyl-D-aspartate (NMDA) receptor antagonist used in the management of Alzheimer's Disease (AD). It is different from many other Alzheimer's Disease medications, as it works by a different mechanism than the cholinesterase enzyme inhibitors normally employed in the management of Alzheimer's disease [A1639]. Memantine blocks the effects of glutamate, a neurotransmitter in the brain that leads to neuronal excitability and excessive stimulation in Alzheimer's Disease [T556]. In 2010, it was estimated that 36 million people worldwide live with Alzheimer's Disease. In 2013, this number increased to 44 million. Almost doubling every 20 years, the prevalence of Alzheimer's Disease is predicted to reach 66 million by 2030 and to 115 million by 2050 [F4366]. In December 2013, the G8 dementia summit concluded that dementia should be considered a global priority with the objective of developing a cure or a disease-modifying therapy by the year 2025 [L5953, F4366].
Indications and Usage For the treatment of moderate to severe dementia of the Alzheimer's type.
Marketing Status Prescription; Discontinued
ATC Code N06DX01
DrugBank ID DB01043
KEGG ID D08174
MeSH ID D008559
PubChem ID 4054
TTD Drug ID D01JEU
NDC Product Code 0615-8192; 0904-6505; 53746-173; 60687-173; 0615-8319; 65162-173; 60687-184; 65015-892; 53746-169; 0904-6506; 24196-184; 65162-169; 70518-3297; 55111-596; 55154-7637; 55111-597
Synonyms Memantine | Memantin | 1,3-Dimethyl-5-aminoadamantane | 1-Amino-3,5-dimethyladamantane | Namenda | Ebixa | Memantine Hydrochloride | Axura | D-145 | D 145 | D145
Chemical Information
Molecular Formula C12H21N
CAS Registry Number 19982-08-2
SMILES CC12CC3CC(C1)(CC(C3)(C2)N)C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Psychomotor hyperactivity19.11.02.003; 17.01.02.0110.001729%Not Available
Psychotic behaviour19.03.01.0030.000576%Not Available
Pulmonary embolism22.06.02.001; 24.01.06.0010.005764%Not Available
Pulmonary oedema22.01.03.003; 02.05.02.0030.001441%
Pulse abnormal13.14.04.004--Not Available
Pulse pressure decreased13.14.04.008--Not Available
Purpura24.07.06.005; 23.06.01.004; 01.01.04.003--
Pyrexia08.05.02.0030.004612%
Pyuria20.02.01.012; 11.01.08.043--Not Available
Rash23.03.13.001--Not Available
Rash erythematous23.03.06.003--Not Available
Rectal haemorrhage24.07.02.018; 07.12.03.001--
Reflexes abnormal17.02.01.006--Not Available
Renal cyst20.01.04.001; 16.27.01.001--Not Available
Renal failure20.01.03.005--Not Available
Respiratory disorder22.02.07.0020.000576%Not Available
Respiratory distress22.02.01.0120.000576%Not Available
Respiratory failure22.02.06.002; 14.01.04.0030.000451%
Retinal detachment12.01.04.004; 06.09.03.003--
Retinal haemorrhage24.07.05.003; 06.10.01.001--Not Available
Rhabdomyolysis15.05.05.0020.001729%
Rhinitis22.07.03.006; 11.01.13.004--
Sciatica17.10.03.001; 15.10.01.001--Not Available
Sedation17.02.04.0050.001729%Not Available
Seizure17.12.03.0010.004035%
Sensory disturbance17.02.07.006--Not Available
Sensory loss17.02.07.007--Not Available
Sepsis11.01.11.0030.000827%
Septic shock24.06.02.011; 11.01.11.0040.000226%Not Available
Shock24.06.02.002--Not Available
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