321 จำนวนผู้เข้าชม |
31/01/2024
Memory refers to cognitive mechanisms involving the intake, storage, and retrieval of information. There are various types of memory, including:
As individuals age, memory or learning abilities may decline, leading to memory decline or mild forgetfulness (also termed age-related memory decline).
Age-related memory issues may stem from physical changes in the brain such as:
Other contributing factors include:
When memory loss is severe and unrelated to normal aging, medical consultation is necessary.
Drugs like Donepezil, Galantamine, and Rivastigmine inhibit the breakdown of acetylcholine, enhancing neurotransmission in brain areas involved with memory and learning. They are mainly used for treating Alzheimer’s disease.
| Drug | Initial Dosage and Titration | Administration |
|---|---|---|
| Donepezil | Start: 5 mg once daily at bedtime; increase to 10 mg once daily after at least 1 month. | With or without food |
| Rivastigmine | Start: 1.5 mg twice daily; increase by 1.5 mg every two weeks to a maximum of 6 mg twice daily. Restart with 1.5 mg twice daily if interrupted. | With food |
| Galantamine (Tab) | Start: 4 mg twice daily for 4 weeks, then increase to 8 mg twice daily; may titrate to 12 mg twice daily. | With food |
| Galantamine (MR cap) | Start: 8 mg once daily for 4 weeks, then increase to 16 mg once daily; max 24 mg once daily. | With food |
Common side effects include dizziness, headache, nausea, vomiting, loss of appetite, and diarrhea.
Use should be avoided in patients with severe renal or hepatic impairment, epilepsy, cardiovascular disease, and in pregnant or breastfeeding women.
N-methyl-D-aspartate (NMDA) receptor antagonists, such as memantine, may be considered for patients with moderate to severe Alzheimer’s disease.
| Drug | Initial Dosage and Titration | Administration |
|---|---|---|
| Memantine | Start: 5 mg once daily; increase by 5 mg weekly to a max of 20 mg/day. | With or without food |
Common side effects include dizziness, headache, nausea, vomiting, loss of appetite, and diarrhea.
Use should be avoided in patients with severe renal or hepatic impairment, epilepsy, cardiovascular disease, Alkaline urine conditions, and in pregnant or breastfeeding women.
Additionally, co-administration with other NMDA antagonists (e.g., dextromethorphan, ketamine) should be avoided.
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