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SOP prepared by SOP reviewed by
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Signature Signature
Date SOP prepared SOP reviewed date
SOP version number SOP version number
Scope
This SOP sets out the process for conducting legal and clinical checks of prescriptions
This SOP does not cover:
o Other aspects of the dispensing process – refer to relevant SOP
o Conducting legal and clinical checks of veterinary prescriptions – refer to the relevant SOP
Guidance
IMPORTANT: The RP must be signed in to be able to undertake a legal and clinical check of a prescription
Refer to the “delegation of responsibilities” notes to ensure that for each action/activity to be delegated, it
takes into account the competency of the relevant team member to carry out that action/activity
Refer to the relevant NPA resources and guidance documents for checking the legal requirements for
prescriptions, including EEA prescriptions — available from the NPA website SOPs section
Legal check
NHS and private prescriptions are valid for 6 months
NHS and private prescriptions for Schedule 2, 3 or 4 Controlled Drugs (CDs) are valid for 28 days
Private repeat prescriptions are legally valid until either all repeats have been dispensed or in accordance with
the prescriber’s directions as long as the initial dispensing occurs within 28 days of the appropriate date for
Schedule 4 CDs and six months for other items
o However, it may not always be clinically appropriate to dispense outstanding repeats if a significant period of
time has elapsed since the prescription was issued as the patient’s health may have changed; the prescriber
should be contacted to verify if the prescribed item is still clinically suitable for the patient
Ensure the prescriber is entitled to prescribe the item(s) on the presenting prescription form (NHS/private), by
checking their registration entry on the relevant regulatory body website:
o Dentists: https://www.gdc-uk.org/
o Doctors: www.gmc.org.uk
o Nurses and midwifes: www.nmc.org.uk
o Other: www.hcpc-uk.co.uk
o EEA and Swiss prescribers: The General Medical Council (GMC) and General Dental Council (GDC) have
contact details of equivalent EEA regulatory bodies on their website
Clinical check
The clinical assessment should be conducted before the accuracy check. Check the patient’s suitability for the
prescribed treatment using appropriate sources; for example, PMR, Summary Care Record (SCR), speak with the
patient etc.
When making the clinical assessment, take the following into consideration to determine the appropriateness of
item(s) prescribed for patient’s condition:
© The National Pharmacy Association July 2017
o Specific patient groups, including children, elderly, pregnant/breastfeeding women, immunocompromised or
palliative care patients
o Presence of concomitant disease, for example, renal and/or hepatic impairment that may require dose
adjustments
o Known allergies, dietary intolerances, personal preferences or requirements due to religious beliefs
o Contraindications and special warnings for use
o Interactions, including other prescribed or over-the-counter item(s),herbal remedies, supplements, or
products purchased online
o Item(s) particulars, such as dose, form, administration route, quantity prescribed
o For high risk medicines, such as anticoagulant therapy, insulin, methotrexate or lithium, refer to the relevant
patient safety SOPs
Use appropriate references to obtain clinical information; these may include:
o Summary of Product Characteristics – available via the eMC website (www.medicines.org.uk) or the
Medicines & Healthcare products Regulatory Agency (MHRA) website (www.mhra.gov.uk/spc-pil)
o The British National Formulary (BNF) and The British National Formulary for Children (BNFC)
o NICE Clinical Knowledge Summaries (CKS) guidelines
o External reference sources, for example, the NPA Pharmacy Services team on 01272 891 800
Prescription interventions
In circumstances where the prescription is not clinically appropriate to dispense, and an intervention is made,
record the actions taken / advice given / interventions and referrals made where considered clinically
appropriate – it is a contractual requirement to make these records in England and Wales
Consider the potential for an Intervention Medicine Use Review (MUR) if appropriate – refer to relevant MUR
SOP
Refer to
relevant
dispensing SOP