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Fever occurs every third day due to rupture of infected red blood cells.

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Drug trials therefore continue after a drug is on the market through monitoring by the MHRA of the first patients using new drugs and through the yellow card scheme of reporting adverse reactions thereafter.

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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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