BOXED WARNING Lithium toxicity is closely related to serum lithium levels and can occur at doses close to therapeutic levels. Facilities for prompt and accurate serum lithium determinations should be available before initiating therapy.
FDA dosing
Population
Start
Target
Max
Acute mania
900 mg BID (or 600 mg TID)
1800 mg/day; serum lithium 1.0-1.5 mEq/L
Serum should not exceed 2.0 mEq/L during acute phase
Long-term control (maintenance)
600 mg BID (or TID up to 1200 mg/day)
900-1200 mg/day; serum lithium 0.6-1.2 mEq/L
Renal Use with caution and reduced dosage; substantially excreted by kidney and toxicity risk greater with impaired renal function - monitor
Hepatic Undefined (not specifically addressed)
Dose individualized by serum lithium concentration and clinical response
Instructions
Swallow extended-release tablets whole; never chew or crush
Maintain normal diet including salt and adequate fluid intake (2500-3500 mL), especially during initial stabilization
Draw serum lithium 8-12 hours after previous dose; monitor twice weekly during acute phase and at least every 2 months during maintenance
Reduce or suspend dose during febrile illness, protracted sweating, or diarrhea
Encephalopathic syndrome with neuroleptics (e.g., haloperidol)
Serotonin syndrome with serotonergic drugs/MAOIs
May prolong effects of neuromuscular blocking agents
Increased toxicity with diuretics, ACE inhibitors, ARBs, NSAIDs
Adverse reactions
Fine hand tremor
Polyuria
Thirst/polydipsia
Nausea
Diarrhea
Vomiting
Drowsiness
Muscular weakness
Lack of coordination
Pregnancy May cause fetal harm; lithium birth registries suggest an increase in cardiac and other anomalies, especially Ebstein's anomaly.
Lactation Lithium is excreted in human milk; nursing not recommended except in rare circumstances; toxicity signs (hypertonia, hypothermia, cyanosis, ECG changes) reported in some infants/neonates.
⚠ BOXED WARNING
Lithium toxicity is closely related to serum concentration and can occur at doses close to therapeutic levels