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Animal studies do not indicate direct or indirect harmful effects with respect to reproductive toxicity see section 5.
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The responsibilities of the independent prescriber are given below: Initial clinical assessment and diagnosis of the patient Agreement with the supplementary prescriber about the limits of their responsibility Provision of advice and support to the supplementary prescriber Review of patients progress at appropriate intervals with the supplementary prescriber if possible Sharing patients records with supplementary prescriber Reporting of adverse drug reactions.
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It is up to individuals to negotiate with their employer that supplementary prescribing should form part of their job. Before becoming eligible to prescribe, they must successfully complete an approved supplementary prescribing training course including all assessments and the period of learning in practice.
The following information must be written on the POM label: Name of patient Name and address of supplier Containers must be clean, sound and fit for the intended purpose. Where possible pharmacies will fit child resistant closures and these must be used for medicines containing aspirin and paracetamol. Fluted bottles must be used for medicines that are for external use only. Patient information leaflets or summary of product characteristics must be included. Their content is set out by law.