药事管理（Pharmaceutical Administration）.docVIP

药事管理（Pharmaceutical Administration） 1. definitions of prescription drugs: prescription drugs refer to drugs that can be purchased, deployed and used by practitioners and practicing physician assistants. 2. non prescription drugs, non prescription drugs: definition refers to promulgated by the drug supervision and Administration Department of the State Council, without prescriptions by licensed doctors or assistant medical practitioners, consumers can decide, purchase and use of drugs. According to the safety of drugs, OTC drugs are classified into two types: armour and B.. 3. the national essential medicine WHO defines essential drugs as: essential drugs are those that satisfy most of the populations health care needs.. Therefore, applications should be available at any time with sufficient amounts and suitable dosage forms. 4. included in the basic medical insurance drug list of the drug is a variety of national drug standards and imported drugs, and in accordance with the clinically necessary, safe and effective, reasonable price, easy to use, can ensure the supply of the market principle. The catalogue of drugs is classified into class a and class B. 5. quality characteristics of drugs: (1) effectiveness: (2) safety (3), stability (4) uniformity 6. main contents of the national drug policy (1) legislation and drug supervision and Administration (2) the choice of essential drugs (3) supply of essential drugs; (4) rational use of drugs (5) pharmacological strategy (6) human resource management; (7) monitoring and evaluation of policy implementation; (8) international cooperation and exchange 7., the concept of essential drugs is relatively abstract and specific: (1) essential drugs are the most necessary medicines to meet the basic medical and health needs of the overwhelming majority of the population; (2) which drugs should be taken as the basic drugs should be adapted to local conditions; (3) essential medicines should be carefully screened and determined in acc