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In this situation, the patient shows a response, which can be described under one of the classical definitions of allergic response (that is, type see below). Such reactions require initial exposure to the drug to cause sensitization, after which, subsequent exposure to the same drug triggers an immunological reaction.

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The information that must be contained in all PGDs is listed below: Name of the business to which the direction applies; Date the direction comes into force and the date it expires; Description of the medicine(s) to which the direction applies; Class of health professional who may supply or administer the medicine; Signature of a doctor and a pharmacist; Signature on behalf of an appropriate organization; Clinical condition or situation to which the direction applies; Description of those patients excluded from treatment under the direction; Description of the circumstances in which further advice should be sought from a doctor, and arrangements for referral; Details of appropriate dosage and maximum total dosage, quantity, pharmaceutical form and strength, route and frequency of administration, and minimum or maximum period over which the medicine should be administered; Relevant warnings, including potential adverse reactions; Details of any necessary follow-up action; and the circumstances; Statement of the records to be kept for audit purposes.

Examples of PGDs relevant to podiatric surgery are shown in Appendix C.

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