Cannabidiol
Brand names: Epidyolex
Cannabidiol is a non-psychoactive cannabinoid licensed as adjunctive therapy for seizures associated with Lennox-Gastaut syndrome, Dravet syndrome and tuberous sclerosis complex, used with clobazam in some indications.
Adult dose
Paediatric dose
Dose adjustments
Cannabidiol can be administered to patients with mild, moderate or severe renal impairment without dose adjustment. There is no experience in patients with end-stage renal disease, and it is not known if cannabidiol is dialysable.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
The UK SPC dose is weight-based and identical for adults and children: 2.5 mg/kg twice daily (5 mg/kg/day) for one week, then 5 mg/kg twice daily (10 mg/kg/day), with further weekly increments of 2.5 mg/kg twice daily (5 mg/kg/day) as clinical response and tolerability allow. AGE LIMITS - LGS and DS: there is no relevant use in children aged below 6 months, and the safety and efficacy in children aged 6 months to 2 years have not yet been established (no data available). TSC: there is no relevant use in children aged below 1 month, and the safety and efficacy in children aged 1 month to 2 years have not been established - data in patients aged 1 to 2 years exist but no recommendation on a posology can be made. Dose increases above 10 mg/kg/day require adherence to the full liver-function monitoring schedule. Reduced doses apply in moderate and severe hepatic impairment (see adult notes). Verify against a children's formulary before use.
Contraindications
- Hypersensitivity to the active substance or to any of the excipients
- Patients with transaminase elevations greater than 3 times the upper limit of normal (ULN) and bilirubin greater than 2 times the ULN
Side effects
- Somnolence, including sedation (very common)
- Decreased appetite (very common); weight decreased (common)
- Diarrhoea and vomiting (very common); nausea (common)
- Pyrexia and fatigue (very common); lethargy (common)
- Hepatocellular injury - dose-related elevations of ALT, AST and GGT (common); ALT elevations above 3 times the ULN occurred in 12% of cannabidiol-treated patients versus less than 1% on placebo, and transaminase elevation was the most frequent cause of discontinuation; fewer than 1% had ALT or AST greater than 20 times the ULN, and there have been cases associated with hospitalisation
- Seizure, irritability, aggression, cough, rash, pneumonia and urinary tract infection (common)
Interactions
- Valproate - the majority of ALT elevations in clinical trials occurred in patients taking concomitant valproate (ALT elevations greater than 3x ULN in 19% on valproate without clobazam, and 23% on both valproate and clobazam, versus 3% on neither); dose adjustment or discontinuation of valproate should be considered if transaminase elevations occur, and intensified liver monitoring is required
- Clobazam - concomitant use also increased the incidence of transaminase elevations, although to a lesser extent than valproate; clobazam dose adjustment should be considered if transaminase elevations occur
- Other antiepileptic drugs - a physician experienced in treating patients on concomitant antiepileptic drugs should evaluate the need for dose adjustments of cannabidiol or of the concomitant medicinal product(s) to manage potential drug interactions
- Medicinal products known to impact the liver - upon a dose change or addition, the liver-function monitoring schedule should be restarted (as it should upon cannabidiol dose changes above 10 mg/kg/day)
- Food - may increase cannabidiol levels; take consistently either with or without food
- NOTE: SPC section 4.5 was not included in this source bundle; the full interaction section must be reviewed
Clinical monograph
How it works
Its precise antiseizure mechanism is not fully defined but is independent of cannabinoid CB1/CB2 receptors, with effects thought to involve modulation of intracellular calcium and other neuronal signalling pathways.
Prescribing in practice
- Monitor liver function because cannabidiol can cause dose-related hepatocellular transaminase elevations, especially when combined with valproate or clobazam.
- It interacts significantly with clobazam, increasing exposure to the active clobazam metabolite and the risk of sedation.
- Withdraw gradually if discontinuing, as with other antiseizure medicines.
Monitoring
Check liver transaminases and bilirubin before starting and periodically during treatment, with closer monitoring in those on valproate or with pre-existing hepatic impairment.
Counselling the patient
- Attend for blood tests to monitor the liver as advised.
- Report drowsiness, loss of appetite, jaundice or abdominal pain.
- Do not stop the medicine abruptly without specialist advice.
Evidence & guidelines
Efficacy in Dravet and Lennox-Gastaut syndromes was demonstrated in randomised placebo-controlled trials, and it is recommended in specific NICE technology appraisals.
Reference: NICE TA614/TA615/TA681; ABN; RCPCH; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Acute Stroke / TIA Assessment · NICE NG128; RCP Stroke Guidelines 2023
- Status Epilepticus (Adults) · NICE CG137; ESEM guidelines; RCP Neurology Guidelines
- Suspected Subarachnoid Haemorrhage · NICE NG228; RCEM 2023; AHA/ASA 2023
- Adult Head Injury · NICE NG232 (2023)
- Bell's Palsy / Facial Nerve Palsy · ENT UK 2017; AAN
- Vertigo Workup · ENT UK; NICE CKS