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Drugs carbamazepine

Many authors reported poor elimination of antiepileptic drug carbamazepine [6,13,17,49, 54]. Pharmacokinetic data indicate that only 1-2% of carbamazepine is excreted unmetabolized. However, glucuronide conjugates of carbamazepine can presumably be cleaved in the sewage, and thus increase its environmental concentrations [51]. This is confirmed by its high ubiquity in the enviromnent at concentration levels of several hundred nanograms per liter in different surface waters. Due to its recalcitrant nature, it can be used as anthropogeiuc marker for the contamination of aquatic environment. [Pg.207]

The first mood stabilizer was lithium (its antimanic action being discovered in 1948) more recently the anticonvulsant drugs carbamazepine and valproate have been found to be effective in acute mania. Unfortunately these mood stabilizers are only successful in controlling mania to a limited extent and few patients are well enough to leave hospital at the end of 3 weeks of treatment using these drugs as monotherapy. It is increasingly common for combination treatment to be advocated, in which an antipsychotic dmg is combined with lithium or an anticonvulsant. [Pg.71]

Laboratory experiments on the ozonization of the dibenzoazepine drug carbamazepine (McDowell et al. 2005) showed the occurrence of a number of transformation products that were initiated by reaction at the olefinic double bond between the rings (Figure 1.29). [Pg.30]

Psychiatric drugs Carbamazepine P. chrysosporium Erlenmeyers flasks containing 1 mg L 1 Completely removed [4]... [Pg.200]

Vogna D, Marotta R, Andreozzi R, Napolitano A, d Ischia M (2004) Kinetic and chemical assessment of the UV/H2O2 treatment of antiepileptic drug carbamazepine. Chemosphere... [Pg.68]

Ozonation of the antiepileptic drug carbamazepine resulted in the formation of three main DBFs l-(2-benzaldehyde)-4-hydro-(7//,i//)-quinazoline-2-one, l-(2-benzaldehyde)-(7/7,5/7)-quinazoline-2,4-dione, and l-(2-benzoic... [Pg.114]

Oxidation Athene Epoxidation. Alkenes may react to produce epoxides (alternatively, sometimes, the alkenes do not react and are metabolically stable). The epoxide is unstable and is subject to ring opening via a nucleophilic attack. The anticonvulsant drug carbamazepine is metabolized via epoxidation to yield carbamazepine-10,11-epoxide in turn, this is rapidly opened to yield carbamazepine-10,ll-diol. [Pg.147]

Toxic epidermal necrolysis occurs when the skin epidermis is destroyed by the action of toxicants and becomes detached from the dermis. This condition severely disrupts the ability of skin to regulate the release of heat, fluids, and electrolytes. Metabolites of the anticonvulsive drug carbamazepine have been implicated in toxic epidermal necrolysis. [Pg.206]

Enzyme-inducing antiepiieptic drugs (carbamazepine itseif as weii as phenobarbitai, phenytoin, and primidone) may increase the ciearance of carbamazepine and iower its piasma ieveis... [Pg.49]

Enzyme-inducing antiepileptic drugs (carbamazepine, phenytoin, phenobarbital, and primidone) may decrease plasma levels of zonisamide... [Pg.526]

Rustichelli, C., Gamberini, G., Ferioli, V., Gamberini, M. C., Ficarra, R. and Tommasini, S. (2000). Solid state study of polymorphic drugs carbamazepine. J. Pharm. Biomed. Anal, 23,41-54. [148, 250]... [Pg.380]

Epilepsy is a common co-morbid illness in patients who have both psychiatric illness and learning disabilities. The necessary combination of the anti-epilepsy drug carbamazepine, a CYP 3A4 enzyme inducer, with a CYP 3A4 inhibiting SSRI antidepressant then calls for particularly careful increment in drug doses supported by monitoring of plasma carbamazepine concentration. [Pg.378]

Individual drugs carbamazepine, phenytoin, sodium valproate, lamotrigine, vigabatrin, gabapentin, clonazepam, topiramate, levetiracetam. [Pg.413]

Visual field defects associated with various antiepUeptic drugs (carbamazepine, diazepam, gabapentin, pheny-toin, tiagabine, and vigabatrin) have been reviewed (19). The true frequency is unknown, but in a retrospective study in 158 patients with partial epilepsy visual field defects were detected in 21 (13%) 13 patients had concentric visual field constriction without subjective spontaneous manifestations. Of these 13 patients, 9 were taking vigabatrin. [Pg.277]

The rationale and use of modified-release formulations of antiepileptic drugs (carbamazepine, valproic acid, and tiagabine) have been reviewed (171). The authors concluded that modified-release formulations afford the advantages of better patient compliance, fewer adverse effects, and less fluctuation in plasma concentrations, making monitoring of drug concentrations easier. They concluded that these advantages should lead to better seizure control and improved quahty of life. [Pg.289]

Zaworotko has recently demonstrated the ability of the drug carbamazepine to form a crystalline homodimer.43 The structure was sustained by an amide dimer synthon (Fig. 23). The dimer possessed two pendant NH groups that participated in hydrogen bonds with solvent molecules (e.g. acetone). The solids were generated to develop new solid compositions of the drug. Such compositions are anticipated to lead to pharmaceutical materials that exhibit properties (e.g. bioavailability) not realized by previous crystalline forms of the drug molecule. [Pg.31]

Potschka, H., Fedrowitz, M., and Loscher. W. (2001) P-glycoprotein and multidrug resistance-associated protein are involved in the regulation of extracellular levels of the major antiepileptic drug carbamazepine in the brain. Neuroreport, 12 (16). 3557-3560. [Pg.409]

Na+ Anticonvulsant drugs Class I antiarrhythmics Diuretic drugs Local anesthetic drugs Carbamazepine, phenytoin, valproic acid lA Disopyramide, procainamide, quinidine IB Lidocaine, mexiletine, phenytoin, tocainide IC Encainide, flecainide, propafenone Amiloride Bupivacaine, cocaine, lidocaine, mepivacaine, tetracaine... [Pg.15]


See other pages where Drugs carbamazepine is mentioned: [Pg.186]    [Pg.157]    [Pg.222]    [Pg.146]    [Pg.90]    [Pg.70]    [Pg.174]    [Pg.110]    [Pg.324]    [Pg.170]    [Pg.178]    [Pg.299]    [Pg.174]    [Pg.112]    [Pg.550]    [Pg.174]    [Pg.161]    [Pg.215]    [Pg.104]    [Pg.767]    [Pg.124]    [Pg.326]    [Pg.416]    [Pg.396]    [Pg.284]    [Pg.776]    [Pg.2460]    [Pg.2456]    [Pg.477]    [Pg.664]   
See also in sourсe #XX -- [ Pg.300 ]




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Carbamazepin

Carbamazepine

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