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Download Pharmacy Curriculum Draft (NCRC); 2011

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a. Intravenous Injection (Bolus) b. Intravenous infusion.II. Multicompartment models.a. Two compartment open model.b. IV bolus, IV infusion and oral administrationIII. Non-compartmental Model.Statistical Moment Theory; MRT for various compartment models;Physiological Pharmacokinetic model.8. MULTIPLE DOSAGE REGIMENa. Introduction, principles of superpositionb. Factors: persistent, accumulation and loss factorsc. Repetitive Intravenous injections – One Compartment Open Modeld. Repetitive Extravascular dosing – One Compartment Open modele. Multiple Dose Regimen – Two Compartment Open Model9. ELIMINATION OF DRUGS:a) Hepatic Elimination. Percent of Drug Metabolized, DrugBiotransformation reactions, (Phase-I reactions and phase-II reactions),First pass effect, Hepatic clearance of protein bound drugs and Biliaryexcretion of drugs.b) Renal Excretion of Drugs: Renal clearance, Tubular Secretion andTubular Reabsorption.c) Elimination of Drugs through other organs: Pulmonary excretion,Salivary excretion, Mammilary excretion, Skin excretion and Genitalexcretion.10. PROTEIN BINDING: Introduction, types, kinetics, determination andclinical significance of drug-protein binding.11. PHARMACOKINETICS VARIATIONS IN DISEASE STATES.Determination of pharmacokinetics variations in renal and hepatic diseases,general approaches for dose adjustment in renal diseaseand hepatic diseases.12. PHARMACOKINETICS OF INTRAVENOUS INFUSIONS.13. BIOPHARMACEUTICAL ASPECTS INDEVELOPING A DOSAGEFORMDrug considerations, drug product considerations, patient considerations,manufacturing considerations, pharmacodynamic considerationspharmacokinetic considerations156 | Pakistan Pharmacist Federation; www.pharmacistfed.pk,www.pharmafed.wordpress.com, www.pharmarev.com, info@pharmacistfed.pk,

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