section name header

Pronunciation

LITH-ee-um audio

Indications

REMS

Action

Therapeutic Effects:

Pharmacokinetics

Absorption: Completely absorbed after oral administration.

Distribution: Widely distributed into many tissues and fluids; CSF levels are 50% of plasma levels. Crosses the placenta; enters breast milk.

Metabolism/Excretion: Excreted almost entirely unchanged by the kidneys.

Half-life: 20–27 hr.

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: ECG changes, arrhythmias, edema, hypotension, unmasking of Brugada syndrome.

Derm: DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), acneiform eruption, folliculitis, alopecia, diminished sensation, pruritus.

EENT: aphasia, blurred vision, dysarthria, tinnitus.

Endo: hypothyroidism, goiter, hyperglycemia, hyperparathyroidism, hyperthyroidism.

F and E: hypercalcemia, hyponatremia.

GI: abdominal pain, anorexia, bloating, diarrhea, nausea, dry mouth, metallic taste.

GU: polyuria, glycosuria, nephrogenic diabetes insipidus, renal impairment.

Hemat: leukocytosis.

Metab: weight gain.

MS: muscle weakness, hyperirritability, rigidity.

Neuro: tremors , PSEUDOTUMOR CEREBRI, SEIZURES, fatigue, headache, impaired memory, ataxia, sedation, confusion, dizziness, drowsiness, psychomotor retardation, restlessness, stupor.

Misc: SEROTONIN SYNDROME.

Interactions

Drug-Drug:

Drug-Natural Products:

Drug-Food:

Route/Dosage

see Calculator

Precise dosing is based on serum lithium levels. 300 mg lithium carbonate contains 8–12 mEq lithium

Implementation

US Brand Names

Lithobid

Canadian Brand Names

Carbolith, Lithane, Lithmax

Classifications

Therapeutic Classification:

Availability

(Generic available)

Time/Action Profile

(antimanic effects)

ROUTEONSETPEAKDURATION
PO, PO–ER5–7 days10–21 daysdays

Assessment

Lab Test Considerations: Toxicity and Overdose:

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code*