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    Tegretol


    carbamazepin \  المادة الفعالة

     
    مضاد للتشنجات

    tegretol 200 mg ( 20 tab ) >>> 11 L.E

    tegretol CR 200 mg ( 20 tab ) >>> 16 L.E

    tegretol CR 400 mg ( 10 tab ) >>> 12 L.E

    tegretol 100 mg / 5 ml ( syrup ) >>> 8 L.E
    Class of drug: Anticonvulsant, analgesic.

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    Mechanism of action:

    Anticonvulsant action: blocks polysynpatic transmission by inhibiting influx of sodium ions across thecell membrane.



    Analgesic action: blocks polysynpatic transmission within the CNS. Also has anticholinergic, antidiuretic, antiarrythmic, muscle relaxant properties.

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    Indications/dosage/route: Oral only.



    • Epilepsy: tonic–clonic, partial seizures with complex symptoms (psychomotor or temporal lobe seizures)

    Ð Adults, children >12 years: Initial: 200 mg b.i.d.; increase dose weekly by 200 mg/d maximum. Maintenance: 800–1200 mg/d.

    Maximum: 1600 mg/d.

    Ð Children 6–12 years: Initial: 100 mg b.i.d.; increase dose

    weekly by 100 mg/d. Maintenance: 400–800 mg/d. Maximum:

    1000 mg/d.

    • Trigeminal neuralgia (unlabeled use)

    Ð Adults: Initial: 100 mg b.i.d. Maintenance: 200 mg–1.2 g/d.

    Maximum: 1.2 g/d.

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    Adjustment of dosage

    • Kidney disease: creatinine clearance <10 mL/min: 75% of standard dose.

    • Liver disease: None.

    • Elderly: Reduce dose and monitor carefully.

    • Pediatric: Safety and efficacy have not been established in children<6 years.

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    Food: Should be taken with food to prevent GI upset.

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    Pregnancy: Category C. Should be continued during pregnancy if favorable benefits versus risk.

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    Lactation: Present in breast milk. Considered compatible by American Academy of Pediatrics. Should be continued during lactation if favorable benefits versus risk.

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    Contraindications: Bone marrow depression, use of MAO inhibitor within 14 days, cross-sensitivity with tricyclic antidepressants, hypersensitivity to carbamazepine.

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    Warnings/precautions

    • Use with caution in patient with the following conditions: mixed type seizures, liver and cardiac disease.

    • Carbamazepine should be discontinued if WBC is <3000 and neutrophils <=1500.

    • Abrupt withdrawal may precipitate seizures.

    • Aplastic anemia and agranulocytosis are significant risks in using carbamazepine.

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    Advice to patient

    • To minimize possible photosensitivity reaction, apply adequate sunscreen and use proper covering when exposed to strong sunlight.

    • If you are receiving an oral contraceptive, use an alternative method of birth control.

    • Avoid alcohol and other CNS depressants such as opiate analgesics and sedatives (eg, diazepam) when taking this drug.

    • Avoid driving and other activities requiring mental alertness or that are potentially dangerous until response to drug is known.

    • Notify dentist or treating physician prior to surgery if taking this medication.

    • Do not stop taking this drug without consulting treating physician.

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    Adverse reactions

    • Common: drowsiness, dizziness, ataxia, confusion, nausea, vomiting, rash, blurred vision, nystagmus.

    • Serious: worsening of seizures, bone marrow depression (including aplastic anemia), hepatitis, Stevens–Johnson syndrome, toxic

    epidermal necrolysis, CHF, heart block, arrhythmia.

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    Clinically important drug interactions

    • Drugs that increase effects/toxicity of carbamazepine: isoniazid, cimetidine, diltiazem, verapamil, erythromycin, propoxyphene,

    danazol.

    • Drugs that decrease effects/toxicity of carbamazepine: phenobarbital, phenytoin, primidone, theophylline.

    • Carbamazepine increases effects/toxicity of following: primidone, clomipramine, lithium, phenytoin.

    • Carbamazepine decreases effects/toxicity of following: phenytoin,

    warfarin, doxycycline, theophylline, alprazolam, rifampin,

    cisplatin, oral contraceptives, cyclosporine, clonazepam, valproic acid.







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