Study register · detail
Clear benefit
12 citations
Samplek = 24 Quellen
Durationunclear
EndpointSafety/tolerability
Blindingn.a.
DesignNarrative Review
Cannabinoidkombination
THC:CBD1:1
Routeoromukosal
Key finding
Nabiximols showed good tolerability and a safe profile in the treatment of spasticity and chronic pain in everyday clinical practice, with frequent but expected side effects (dizziness, fatigue, somnolence) and a low rate of serious adverse events (3,1% in MS spasticity studies).
Summary
Systematic review of nabiximols (THC:CBD spray) in MS spasticity; k=24 studies (20 spasticity, 4 pain), n=4.351 MS spasticity patients. Most common side effects: dizziness, fatigue, somnolence. SAE rate 3,1% (137/4.351), 39 treatment-related SAEs in 32 patients (all resolved). No treatment-related SAEs in pain studies.
P
PopulationPersons with multiple sclerosis (spasticity) and/or chronic non-cancer pain; pooled study population from 24 observational studies, registries and case reports, n≈4351+ (spasticity studies)
I
InterventionNabiximols oromucosal spray (THC:CBD 1:1), add-on therapy
O
OutcomeSAE rate in MS spasticity observational studies 3,1% (137/4351); 39 treatment-related SAEs in 32 patients, all (where specified) resolved; no treatment-related SAEs in pain studies; most common ADRs: dizziness, fatigue, somnolence
Quality profile
Sample size
★★★★★
Blinding
—
Effect size
Clear benefit
Citations / year
★★★★★
Authors
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Abstract
Introduction: : Nabiximols oromucosal spray,a cannabis-based medicine containing a balanced ratio of Delta-9-tetrahydrocannabinol and cannabidiol, is approved widely as an add-on therapy for symptomatic relief of spasticity in people with multiple sclerosis (MS). Most safety data for nabiximols derive from use in MS spasticity, with some data available from the analgesia area.
Areas Covered: : This review compiles safety and tolerability data from all published observational studies, registry analyses, and case reports identified in systematic searches in which nabiximols oromucosal spray was investigated for spasticity (n = 20) and/or chronic non-cancer pain (n = 4). Aligning with the known safety profile of nabiximols as demonstrated in randomized controlled trials, common adverse events reported consistently across studies conducted under clinical practice conditions were dizziness, fatigue and somnolence. The serious adverse event (SAE) rate with nabiximols in MS spasticityobservational studies was 3.1% (137/4351). A total of 39 treatment-related SAEs were reported in 32 patients with spasticity, all of which (where specified) were resolved. No treatment-related SAEs were recorded in nabiximols pain studies.
Expert Opinion: : Real-world experience with nabiximols oromucosal spray in treating spasticity and chronic pain indicates that, overall, it is well tolerated and has a good safety profile.
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