Table 31.3—Mood Stabilizers for Behavioral Disturbances in Dementia With Manic Features
|
Drug |
Geriatric Dosage |
Adverse Effects |
Comments |
|
200–1000 mg/day (therapeutic level 4–12 μg/mL) |
Nausea, fatigue, ataxia, blurred vision, hyponatremia |
Poor tolerability in older adults; must monitor CBC, LFTs, electrolytes q 2 weeks for first 2 months, then q 3 months |
|
|
150–1000 mg/day (therapeutic level 0.5–0.8 mEq/L) |
Nausea, vomiting, tremor, confusion, leukocytosis |
Poor tolerability in older adults; toxicity at low serum levels; monitor thyroid and renal function |
|
|
250–2000 mg/day (therapeutic level 40–100 μg/mL) |
Nausea, GI upset, ataxia, sedation |
Requires monitoring of CBC, platelets, LFTs at baseline and q 6 months; better tolerated than other mood stabilizers in older patients |
* Approved by the Food and Drug Administration for the treatment of bipolar disorder.
NOTE: CBC = complete blood cell count; GI = gastrointestinal; LFTs = liver function tests; q = every.