The Selection and Use of Essential Medicines - WHO Technical Report Series, No. 914
(2003; 132 pages) View the PDF document
Table of Contents
View the documentWHO Expert Committee on the Selection and Use of Essential Medicines
View the document1. Introduction
View the document2. Open session
Open this folder and view contents3. The new procedures for updating and disseminating the Model List
Open this folder and view contents4. Other outstanding technical issues
Open this folder and view contents5. Format and presentation of the 12th Model List
Open this folder and view contents6. Changes made in revising the Model List
Open this folder and view contents7. Future reviews of sections of the Model List
Close this folder8. Recommendations
View the document8.1 Procedures for updating and disseminating the Model List of Essential Medicines1
View the document8.2 Description of essential medicines
View the document8.3 Presentation of the 12th Model List
View the document8.4 Additions and changes to the Model List
View the document8.5 Deferred applications
View the document8.6 Rejected applications
View the document8.7 Priorities for future reviews of sections of the Model List
View the document8.8 Change of name of the Expert Committee
View the document8.9 Other recommendations
View the documentAcknowledgements
View the documentReferences
View the documentAnnex 1 The 12th WHO Model List of Essential Medicines
View the documentAnnex 2 Additional notes on the medicines recommended for inclusion in the 12th WHO Model List of Essential Medicines
View the documentAnnex 3 The Anatomical Therapeutic Chemical (ATC) classification system1
View the documentAlphabetical list of essential medicinces (with ATC classification codes)
 

8.7 Priorities for future reviews of sections of the Model List

1. Following the updating of the WHO/ISH clinical guidelines for the treatment of hypertension, the section on antihypertensive medicines should be reviewed.

2. A full review of other categories of cardiovascular medicines should be initiated.

3. In view of the new definition of complementary list medicines and the need for greater consistency in its implementation, a full review of the designation of items as either core or complementary list should be undertaken before a decision is made at the next meeting of the Committee whether to maintain the two separate lists.

4. The use of the square box symbol should become more restricted. To this end, a review of the use of the symbol should be undertaken for the next meeting of the Committee.

5. All injectable medicines on the Model List should be reviewed.

6. A full inventory should be made of all other suggestions for deletions and/or review of sections of the Model List. An electronic consultation should be held to identify the most urgent items or sections for future review through one of the two processes recommended in section 8.1, recommendation 3.

7. The glossary which was contained in previous reports of the Committee, should be updated for the next meeting of the Committee.

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Last updated: May 3, 2013