Drug Guide

Generic Name

Citalopram Hydrobromide

Brand Names Celexa

Classification

Therapeutic: Antidepressant

Pharmacological: Selective Serotonin Reuptake Inhibitor (SSRI)

FDA Approved Indications

Mechanism of Action

Citalopram selectively inhibits the reuptake of serotonin in the central nervous system, increasing serotonergic activity in the synaptic cleft.

Dosage and Administration

Adult: Starting dose typically 20 mg once daily; can be increased up to 40 mg/day based on response and tolerability.

Pediatric: Not FDA-approved for pediatric use; data limited.

Geriatric: Start at a lower dose, e.g., 10 mg/day, and titrate as needed, considering increased sensitivity and risk of side effects.

Renal Impairment: Use with caution; consider dose adjustments, especially in severe impairment.

Hepatic Impairment: Use with caution; start at lower doses with careful monitoring.

Pharmacokinetics

Absorption: Well-absorbed orally, with peak plasma levels in approximately 2-4 hours.

Distribution: Widely distributed; volume of distribution approximately 12 L/kg.

Metabolism: Primarily hepatic via CYP2C19, CYP3A4, and CYP2D6 enzymes.

Excretion: Primarily excreted in urine (cholesterols and conjugates), with a smaller amount in feces.

Half Life: Approximately 35 hours, allowing once-daily dosing.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

Drug-Herb Interactions

Nursing Implications

Assessment: Monitor mood, suicidal thoughts, and side effects; baseline ECG if at risk for QT prolongation.

Diagnoses:

  • Risk for decreased cardiac output related to QT prolongation
  • Risk for injury related to somnolence or dizziness

Implementation: Administer with food if GI upset occurs; monitor for therapeutic response and adverse effects.

Evaluation: Assess improvement in depressive symptoms; monitor for adverse effects, including cardiac issues.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: Variations in CYP2C19 genotype can affect metabolism and plasma levels.

Lab Test Interference: May slightly elevate liver enzymes; routine monitoring recommended in long-term therapy.

Overdose Management

Signs/Symptoms: Nausea, vomiting, dizziness, tremor, arrhythmias, seizures.

Treatment: Supportive care, activated charcoal if within a few hours of ingestion, cardiac monitoring, and symptomatic treatment.

Storage and Handling

Storage: Store at room temperature away from light and moisture.

Stability: Stable for at least 2 years if stored properly.

This guide is for educational purposes only and is not intended for clinical use.