Cannabidiol, the active ingredient in VERSÉA, naturally occurs in the cannabis and hemp plants. The source of cannabidiol used in VERSÉA is industrial hemp. Cannabidiol is a white to pale yellow crystalline solid. It is insoluble in water and is soluble in organic solvents.
VERSÉA (cannabidiol) products come in a number of formulations. The tincture is a semi-clear, water-soluble oral liquid formulation at concentrations of 110mg/1oz for the 3,300mg tincture, 40mg/1oz for the 1,200mg tincture and 20mg/1oz for the 600mg tincture. The salve stick provides 500mg in the 1oz easy application topical formulation and capsules contain 25mg/gel cap. All formulations are broad spectrum, ensuring no THC, are non-GMO, organic and manufactured using pro-absorption technology.
Cannabidiol is metabolized by cytochrome p450 (CYP) enzymes CYP3A4 and CYP2C19. At clinically relevant concentrations, cannabidiol has the potential to inhibit CYP2C8, CYP2C9, and CYP2C19 and may induce or inhibit CYP1A2 and CYP2B6. Cannabidiol inhibits uridin5'-diphospho-glucuronosyltransferase (UGT) enzymes UGT1A9 and UGT2B7 1,2.
Cannabidiol may increase serum concentrations of macrolides, calcium channel blockers, benzodiazepines, cyclosporine, sildenafil (and other PDE5 inhibitors), antihistamines, haloperidol, antiretrovirals, and some statins (atorvastatin and simvastatin, but not pravastatin or rosuvastatin) and other drugs metabolized by CYP3A4. Drugs such as ketoconazol, itraconazol, ritonavir, and clarithromycin inhibit this enzyme, leading to slower CBD degradation, and can consequently lead to higher CBD doses that are longer medically active. In contrast, phenobarbital, rifampicin, carbamazepine, and phenytoin induce CYP3A4, causing reduced CBD bioavailability3.