Drug Guide
Clorazepate Dipotassium
Classification
Therapeutic: Antianxiety agent, anticonvulsant
Pharmacological: Benzodiazepine
FDA Approved Indications
- Anxiety disorders
- Partial seizures
Mechanism of Action
Clorazepate enhances the effect of the neurotransmitter gamma-aminobutyric acid (GABA) at the GABA-A receptor, producing sedative, hypnotic, anxiolytic, anticonvulsant, and muscle relaxant properties.
Dosage and Administration
Adult: Initially, 7.5-15 mg 2-4 times daily; dosage may be increased gradually based on response and tolerability. Typical maintenance doses range from 15-60 mg daily in divided doses.
Pediatric: Use is not established; contraindicated in children.
Geriatric: Start with lower doses, such as 3.75-7.5 mg daily, due to increased sensitivity and risk of sedation and falls.
Renal Impairment: Adjust dose cautiously; monitor for increased sensitivity.
Hepatic Impairment: Use with caution; dose adjustment may be necessary.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed; crosses the blood-brain barrier.
Metabolism: Metabolized in the liver to active metabolites.
Excretion: Excreted primarily in the urine.
Half Life: Approximately 40 hours in healthy adults, but can be longer in the elderly.
Contraindications
- Hypersensitivity to benzodiazepines
- Acute narrow-angle glaucoma
Precautions
- History of substance abuse, severe respiratory impairment, hepatic impairment, pregnancy, lactation, elderly, or debilitated patients. Use cautiously in patients prone to falls or with suicidal tendencies.
Adverse Reactions - Common
- Drowsiness (Common)
- Dizziness (Common)
- Ataxia (Common)
Adverse Reactions - Serious
- Respiratory depression (Rare)
- Anterograde amnesia (Rare)
- Dependence and withdrawal symptoms (Serious with prolonged use)
Drug-Drug Interactions
- CNS depressants (alcohol, opioids, other sedatives) increase risk of sedation and respiratory depression.
- Other benzodiazepines, barbiturates, antipsychotics, antidepressants.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor mental status, level of sedation, respiratory function, and for signs of dependence.
Diagnoses:
- Risk for falls
- Risk for dependence
- Altered sleep pattern
Implementation: Administer with meals if GI upset occurs; avoid alcohol and other CNS depressants; monitor for excessive sedation.
Evaluation: Assess effectiveness in reducing anxiety or seizures; monitor for adverse effects and dependency.
Patient/Family Teaching
- Do not operate heavy machinery or drive until response is known.
- Avoid alcohol and other CNS depressants.
- Recognize signs of overdose and dependence.
- Take medication exactly as prescribed, and do not suddenly stop without medical advice.
Special Considerations
Black Box Warnings:
- Risk of sedation, respiratory depression, and dependence or abuse.
Genetic Factors: None specific.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Extreme sedation, confusion, coma, respiratory depression, hypotension.
Treatment: Supportive care, airway management, dopamine or flumazenil administration (for benzodiazepine overdose), monitor vital signs, and provide respiratory support as needed.
Storage and Handling
Storage: Store at room temperature, away from moisture, heat, and light.
Stability: Stable under recommended storage conditions.