Table 4.
Classification and characteristics of AED-associated ADRs
| ADR Type | Characteristics | Representative Drugs | Typical ADRs | Management Strategy | Remarks |
|---|---|---|---|---|---|
| Type A | Dose-dependent, predictable, related to drug action | Phenytoin, Carbamazepine | Drowsiness, ataxia, tremors, GI symptoms | Dose adjustment, slow titration, symptomatic management | Most common ADR type (~ 30%) [22] |
| Type B | Idiosyncratic, immune/genetic-related, unpredictable | Lamotrigine, Valproic acid | SJS/TEN, hepatotoxicity, aplastic anemia | Immediate drug discontinuation, antihistamines, supportive care | Genetic screening recommended (e.g., HLA-B*1502 for lamotrigine-related SJS) [23, 24] |
| Type C | Chronic cumulative effects, related to long-term use | Phenobarbital, Phenytoin | Osteoporosis, gingival hyperplasia, cognitive impairment | Long-term monitoring (bone density, cognition), calcium/Vitamin D supplementation | Higher risk in elderly patients [25] |
| Type D | Delayed toxicity (months to years), genetic or developmental impact | Valproic acid, Phenytoin | Teratogenicity, carcinogenicity, neurodevelopmental abnormalities | Avoid in pregnancy; enhanced fetal monitoring | Valproic acid poses a teratogenic risk of up to 10% [26] |
ADR: Adverse Drug Reaction