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A kardex (plural kardexes) is a genericised trademark for a medication administration record. [2] The term is common in Ireland and the United Kingdom.In the Philippines, the term is used to refer the old census charts of the charge nurse usually used during endorsement, in which index cards are used, but has been gradually been replaced by modern health data systems and pre-printed charts and ...
Pharmaceutical codes are used in medical classification to uniquely identify medication. They may uniquely identify an active ingredient, drug system (including inactive ingredients and time-release agents) in general, or a specific pharmaceutical product from a specific manufacturer.
Medication barcodes must have specified information for drug identification. Barcode information on these items must include the National Drug Code (NDC) number of the drug, an 11-character identification number for the medication. The NDC contains the name of the medication, dosage and drug company that produces the medication.
send or dispense, e.g. number of tablets provided Can be confused with m,. misce, context-dependent mane: mane: in the morning max. maximum maximum mcg microgram: recommended replacement for "μg" which may be confused with "mg" mdi metered dose inhaler m.d.u. more dicto utendus: to be used as directed mEq milliequivalent mg
Alternate drug classification systems include the AHFS Drug Information brand run by the American Society of Health-System Pharmacists and First DataBank's Generic Sequence Number (GSN) also known as the Clinical Formulation ID or formerly as Generic Code Number Sequence Number (GCN Seq No).
The implementation of BCMA has shown a decrease in medication administration errors in the healthcare setting. [6] Bar codes on medication have federal government guidelines that are reflected within the bar code packaging. [7] The first few digits are used to identify the labeler, this code is issued by the Food and Drug Administration.
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The national drug code is a unique 10 or 11 digit, 3-segment numeric identifier assigned to each medication listed under Section 510 of the US Federal Food, Drug, and Cosmetic Act. The segments identify the labeler or vendor, product (within the scope of the labeler), and trade package (of this product).