By Christopher Andrew Langley, Dawn Belcher
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It is divided into 13 parts (including the general notes) as detailed below. General notes The General Notes section contains background information on what may and may not be supplied on an NHS prescription form and some background information on claims for pay- 37 ments. 1). 1). 1). 1). 1). 1). 1). APP Ch-02 27/8/08 38 10:51 am Page 38 Applied Pharmaceutical Practice Part VII – List of drugs and threshold above which an additional fee will be paid This part contains the list of drugs and threshold above which an additional fee will be paid.
There are many forms currently in use, and changes to the forms occur from time to time. The following sections list the more common forms you are likely to encounter in the different administrations within the UK, although it should be remembered that this list must only be used as a guide as changes may have occurred since the list was compiled. Furthermore, it should be pointed out that some of the codes used in the tables below may be written differently in other publications. 1. 2. 3. originating from the Isle of Man, but not Jersey or Guernsey may be dispensed in England, Wales, Scotland and Northern Ireland.
In these cases, it is usual for patients to be maintained on one particular brand to prevent fluctuations in plasma concentration. See the British National Formulary for further details. 4 If a drug is prescribed in the community using a proprietary name, the proprietary product must be supplied. However, if a drug is prescribed by its generic name, in most cases (except, for example, in the case of some sustained-release preparations), any generic or proprietary equivalent may be supplied. NCSO – No cheaper stock obtainable The only exception to the fixed reimbursement price listed in Part VIII of the Drug Tariff is where in the opinion of the Secretary of State for Health and the National Assembly for Wales there is no product available to pharmacies at the appropriate price (for example if there were manufacturing shortages of a generic item and only a proprietary equivalent was available).
AppliedPharmaceuticalPractice by Christopher Andrew Langley, Dawn Belcher