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close this bookThe Use of Essential Drugs: Eight report of the WHO Expert Committee (WHO - OMS, 1998, 84 p.)
View the document(introduction...)
View the documentWHO Expert Committee on the Use of Essential Drugs - Geneva, 1-5 December 1997
View the document1. Introduction
View the document2. Guidelines for establishing a national programme for essential drugs
View the document3. Criteria for the selection of essential drugs
View the document4. Guidelines for the selection of pharmaceutical dosage forms
Open this folder and view contents5. Quality assurance
Open this folder and view contents6. Reserve anti-infective agents and monitoring of resistance
View the document7. Applications of the essential drugs concept
Open this folder and view contents8. Essential drugs and primary health care
View the document9. Drug donations
View the document10. Post-registration drug studies
Open this folder and view contents11. Research and development
View the document12. Nomenclature
View the document13. Drug information and educational activities
View the document14. Selection and updating of lists of essential drugs
View the document15. Model List of Essential Drugs (tenth list)
View the document16. Considerations and changes made in revising the model list
View the document17. Glossary of terms used in the report
View the documentAcknowledgement
View the documentReferences
View the documentAnnex 1. Application form for inclusion in the Model List of Essential Drugs1
View the documentSelected WHO publications of related interest
View the documentBack Cover

3. Criteria for the selection of essential drugs

The choice of essential drugs depends on many factors, such as the pattern of prevalent diseases; the treatment facilities; the training and experience of the available personnel; the financial resources; and genetic, demographic and environmental factors.

Because of differing views on the definition of an essential drug in terms of what is meant by the “health care needs of the majority” of the population, the model list has been gradually expanded since its introduction. Some drugs are included that are essential only if a therapeutic programme is planned to address the diseases for which these drugs are used. For example, the cytotoxic drugs (section 8.2 of the model list) are essential only if a comprehensive cancer treatment programme is planned. Such a programme requires adequate hospital, diagnostic and clinical laboratory facilities for its implementation. In contrast, the drugs used in palliative care (section 8.4) are always essential, even when a comprehensive cancer treatment programme does not exist.

The selection of essential drugs must always be evidence-based. Only those drugs should be selected for which sound and adequate data on efficacy and safety are available from clinical studies and for which evidence of performance in general use in a variety of medical settings has been obtained.

Each selected drug must be available in a form in which adequate quality, including bioavailability, can be assured; its stability under the anticipated conditions of storage and use must be established.

Where two or more drugs appear to be similar in the above respects, the choice between them should be made on the basis of a careful evaluation of their relative efficacy, safety, quality, price and availability.

In cost comparisons between drugs, the cost of the total treatment, and not only the unit cost of the drug, must be considered. The cost/benefit ratio is a major consideration in the choice of some drugs for the list. In some cases the choice may also be influenced by other factors, such as comparative pharmacokinetic properties, or by local considerations such as the availability of facilities for manufacture or storage.

Most essential drugs should be formulated as single compounds. Fixed-ratio combination products are acceptable only when the dosage of each ingredient meets the requirements of a defined population group and when the combination has a proven advantage over single compounds administered separately in therapeutic effect, safety or compliance.