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2005 Edition Report on Drug Administration Procedure & Practices ...

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cytotoxic and central intravenous admixture services by pharmacy would improve qualityand safety. In additi<strong>on</strong>, a number of issues have been c<strong>on</strong>sidered :(a)(b)(c)Limiting the choices of available drugs in pharmacy and the dose c<strong>on</strong>centrati<strong>on</strong> orstrength for each drug would help to reduce the chances of errors.Complete, updated informati<strong>on</strong> <strong>on</strong> the rec<strong>on</strong>stituti<strong>on</strong>, diluti<strong>on</strong> and compatibility ofintravenous drugs should be supplied by pharmacy to the nurses <strong>on</strong> the wards foreducati<strong>on</strong>al and cross-checking purposes. 1Doctors who have prescribed unc<strong>on</strong>venti<strong>on</strong>al strengths or forms of a drug should bec<strong>on</strong>tacted by a pharmacist in order to discuss for modifying the prescripti<strong>on</strong>.Accuracy in Dispensing4.59 Proper in-house checking procedures should be built into the dispensing system in thepharmacy. The pharmacy staff must remain alert in the process of data entry, as similar drugcodes often give rise to medicati<strong>on</strong> errors. It is important to recognise that the merechecking of the label against the c<strong>on</strong>tent is not sufficient. Reference should always be madeto the ORIGINAL prescripti<strong>on</strong> in checking the end product of the dispensing process for thecorrectness of the drugs and any possible undesirable interacti<strong>on</strong>s am<strong>on</strong>gst them. The doublecheck system should be practised whenever possible.4.60 For high risk drug items e.g. digoxin, or those known to be associated with seriousmedicati<strong>on</strong> errors, all steps in the dispensing process especially the calculati<strong>on</strong> of dose,should be checked independently by another member of the pharmacy staff, preferably apharmacist.4.61 Every prescripti<strong>on</strong> order and all dispensed medicati<strong>on</strong>s should preferably be checked by apharmacist, for detecting and dealing with any potential medicati<strong>on</strong> errors and potentialproblems such as c<strong>on</strong>traindicated drug, drug interacti<strong>on</strong>s. Any necessary clarificati<strong>on</strong> in aprescripti<strong>on</strong> order must be resolved with a doctor before the medicati<strong>on</strong> is dispensed andadministered to the patient.Labelling of Dispensed Medicati<strong>on</strong>s4.62 The labelling of dispensed medicati<strong>on</strong>s allows for the positive identificati<strong>on</strong> of the drug andthe patient to whom the drug is supplied. Proper labelling should be provided <strong>on</strong> alldispensed medicati<strong>on</strong>s in compliance with the requirements of the H<strong>on</strong>g K<strong>on</strong>g MedicalCouncil and the Pharmacy and Pois<strong>on</strong>s Board. The list of requirements for the labelling ofmedicati<strong>on</strong>s is as follows :(a) Name of patient(b) Date of dispensing(c) Trade name or pharmacological name of the drug 2(d) Dosage per unit1 Cross-checking is defined as checking the correctness of the informati<strong>on</strong> or a calculati<strong>on</strong> by a different pers<strong>on</strong>while double-checking is defined as checking the correctness twice by the same pers<strong>on</strong> or by a different pers<strong>on</strong>.2 In HA, this will be in the form of approved pharmacological name or when unavoidable, trade name of the medicati<strong>on</strong>(i.e. in the case of compound preparati<strong>on</strong>). Exempti<strong>on</strong> might be made for approved research when patients have giventheir fully informed c<strong>on</strong>sent, the drug name might not be included.29

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