Fundamentals of Pharmacology for Children's Nurses. Группа авторов

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in Chapter 4 of this text, Medicines Management and the Role of the Healthcare Provider.

      The electronic medicines compendium (emc) contains up‐to‐date, easily accessible information about medicines licensed for use in the UK and can be found at (www.medicines.org.uk/emc). The emc has more than 14,000 documents, all of which have been checked and approved by either the UK or European government agencies which license medicines. These agencies are the UK Medicines and Healthcare products Regulatory Agency (MHRA) and the European Medicines Agency (EMA). The emc is updated continually and you are able to browse for medicines, or active ingredients using the A – Z buttons. The emc contains regulated and approved information on medicines available in the UK including:

      1 Summaries of Product Characteristics (known as SPCs or SmPCs): A SmPC informs healthcare professionals how to prescribe and use a medicine correctly. A SmPC is based on clinical trials that a pharmaceutical company has carried out and gives information about dose, use and possible side effects. A SmPC is always written in a standard format.

      2 Patient Information Leaflets (PILs, Package Leaflets or PLs): A PIL is the leaflet that is included in the pack with any medicine. The PIL is a summary of the SmPC and is written for patients.

      3 Risk Minimisation Materials (RMMs): Risk Minimisation Materials are resources for healthcare professionals that aim to optimise the safe and effective use of a medicine. RMMs can come in a number of forms, such as educational programmes, prescribing or dispensing guides, patient brochures or alert cards.

      4 Safety Alerts: Safety alerts are issued by the medicine healthcare regulatory agency and/or marketing authorisation holder and contain important public health messages or safety critical information about a medicine.

      5 Product Information: This is any additional information about a product. It may include important information such change of packaging or issues related to stock levels. (Electronic Medicines Compendium/Datapharm Ltd.)

      Within the emc there are also audio and video resources that provide additional information in a user‐friendly way, promoting the safe and effective use of a medicine. For example, a video clip may demonstrate how to administer a certain medicine correctly.

      There are hundreds of medicinal products and devices (or appliances) available to treat and manage illnesses, conditions and diseases. A medicinal product is defined as an item which is not considered to be appliance and could be a drug, food, toiletry or type of cosmetic (Pharmaceutical Services Negotiating Committee https://psnc.org.uk/dispensing‐supply/dispensing‐a‐prescription/medicinal‐products/). An approved medical device will carry the CE mark (Conformité Européenne) which signifies that it conforms to the appropriate regulatory standards. Not all of these medical products, devices or appliances are available from the NHS. On receiving a prescription, pharmacy staff will check whether or not an item is allowed to be prescribed on the NHS prior to dispensing using the Drug Tariff.

      The Drug Tariff

      What the Drug Tariff Does

      The Drug Tariff outlines information such as:

       What will be paid to pharmacies for the NHS services provided (for example the cost of drugs and appliances supplied against an NHS Prescription)

       Rules that need to be followed when dispensing items

       Drug and appliance prices

      How to Tell if a Medicinal Product is Allowed on Prescription

      The ‘blacklist’ can be found in Schedule 1 to the NHS Regulations 2004 and is found in the Drug Tariff (part XVIIIA). It is a list of medicinal products which cannot be prescribed on the NHS. Any medicinal product not in the ‘blacklist’ can be prescribed on the NHS. The prescriber may, however, be questioned during the auditing process about the appropriateness of prescribing this item at the NHS’s expense. As a general rule, if a branded (proprietary) product is listed in the ‘blacklist’ it cannot be prescribed on the NHS. Many of the medicinal products on the ‘blacklist’ are available over the counter for people to buy, whilst some do not have enough evidence to show their efficacy.

      If a medicinal product or device is prescribed that is not on the Drug Tariff, it cannot be dispensed.

      Skills in Practice

      Go to the Drug Tariff (www.nhsbsa.nhs.uk/pharmacies‐gp‐practices‐and‐appliance‐contractors/drug‐tariff) and see which of the following products are blacklisted and should not be prescribed on the NHS:

       Ferrous sulfate compound tablets BP

       Gaviscon granules

       Lemsip flu strength

       Lactulose syrup

      The Joint Royal Colleges Ambulance Liaison Committee (JRCALC) Clinical Guidelines

      The Joint Royal Colleges Ambulance Liaison Committee Clinical (JRCALC) Guidelines is a helpful resource for paramedics and other healthcare professionals, in emergency care, on the road and in the community. JRCALC combines expert advice with practical guidance to ensure uniformity in the delivery of high‐quality patient care. The book, available as either a comprehensive reference edition or a pocket guide, covers a wide range of topics, from resuscitation, medical emergencies, trauma, obstetrics and medicines to major incidents and staff well‐being. It includes an extensive UK drugs formulary and Page for Age drugs tables to assist in making medicines administration simple. A digital version, via an app, of the official JRCALC guidelines is also available for

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