Drug Guide
Cannabidiol
Classification
Therapeutic: Anticonvulsant, Neurological disorder treatment
Pharmacological: Cannabinoid
FDA Approved Indications
- Lennox-Gastaut syndrome in patients age 2 years and older
- Dravet syndrome in patients age 1 year and older
Mechanism of Action
Cannabidiol modulates several non-cannabinoid receptors and ion channels, leading to anticonvulsant effects, though its exact mechanism in seizure control is not fully understood.
Dosage and Administration
Adult: Start at 2.5 mg/kg twice daily, titrate up to 10-20 mg/kg twice daily based on response and tolerability.
Pediatric: Initial dose generally 2.5 mg/kg twice daily; titrate gradually.
Geriatric: Data limited; use with caution, start at lower doses, monitor closely.
Renal Impairment: Adjust dosing based on clinical response; no specific guidelines, but cautious titration recommended.
Hepatic Impairment: Liver function should be monitored; dose adjustments may be necessary, especially with concomitant hepatic impairment.
Pharmacokinetics
Absorption: Well absorbed orally, with food increasing bioavailability.
Distribution: Widely distributed; crosses blood-brain barrier.
Metabolism: Primarily metabolized in the liver via CYP2C19, CYP3A4 enzymes.
Excretion: Mainly via feces, minor renal excretion.
Half Life: Approximately 11-20 hours.
Contraindications
- Hypersensitivity to cannabidiol or any component of the formulation.
Precautions
- Liver function abnormalities; monitor ALT and AST, especially at initiation and dose escalation.
- Use with caution in patients with a history of suicidal ideation or behavior.
- Potential for drug interactions, especially with CYP450 substrate drugs.
Adverse Reactions - Common
- Somnolence (Most common, dose-related)
- Decreased appetite (Common)
- Diarrhea (Common)
- Transaminase elevations (Less common, but significant)
- Fatigue (Common)
Adverse Reactions - Serious
- Liver enzyme elevation leading to hepatitis (Rare, but serious)
- Allergic reactions including rash, or hypersensitivity (Rare)
Drug-Drug Interactions
- CYP450 inhibitors or inducers (e.g., ketoconazole, rifampin) can affect cannabidiol levels.
- Other sedatives or CNS depressants may have additive effects.
Drug-Food Interactions
- High-fat meals increase absorption.
Drug-Herb Interactions
N/ANursing Implications
Assessment: Monitor liver function tests (ALT, AST) before and during treatment; assess seizure frequency.
Diagnoses:
- Risk for injury related to seizure activity, sedation.
- Impaired liver function.
Implementation: Start at low dose, titrate slowly. Educate patients on potential side effects and interactions.
Evaluation: Monitor seizure frequency, adverse reactions, and liver function to assess drug efficacy and safety.
Patient/Family Teaching
- Take medication exactly as prescribed, with or without food.
- Report side effects such as mood changes, dizziness, or signs of liver issues.
- Avoid operating machinery until you know how cannabidiol affects you.
- Inform healthcare provider about all other medications being taken.
Special Considerations
Black Box Warnings:
- Hepatotoxicity, including elevations in liver enzymes and potential liver injury.
- Summary of product characteristics emphasizes caution in use, especially in patients with existing liver disease.
Genetic Factors: Metabolism via CYP2C19 may influence drug levels; genetic polymorphisms may affect response.
Lab Test Interference: May elevate liver enzymes; monitor accordingly.
Overdose Management
Signs/Symptoms: Drowsiness, sedation, hypotension, diarrhea.
Treatment: Supportive care; activated charcoal if ingestion is recent; monitoring and symptomatic treatment.
Storage and Handling
Storage: Store at 68°F to 77°F (20°C to 25°C), away from heat, moisture, and light.
Stability: Stable when stored properly, check manufacturer recommendations.