Talk:Bar code medication administration

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This article is or was the subject of a Wiki Education Foundation-supported course assignment. Further details are available on the course page. Student editor(s): TLund, Shilpaus76. Peer reviewers: Trinalynnie, Alliacev.

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 15:17, 16 January 2022 (UTC)[reply]

Five rights?

This is the line I would like to update: Bar code medication administration (BCMA) is a barcode system designed by Glenna Sue Kennick to prevent medication errors in healthcare settings and improve the quality and safety of medication administration. The overall goals of BCMA are to improve accuracy, prevent errors, and generate online records of medication administration. As of the year 2004, hospitals were mandated by the government to start using the BCMA for all prescription drugs.TLund (talk) 20:11, 27 September 2017 (UTC)[reply]

the right medicine at the right dose at the right time by the right route... that's only four "rights". Can someone explain what the fifth "right" is?--Pgallert (talk) 10:11, 12 May 2009 (UTC)[reply]

Right patient — Preceding unsigned comment added by 118.169.98.26 (talk) 01:30, 30 May 2009

I would like to update the website by adding the government regulations for bar code label requirements prior to administrationTLund (talk) 22:47, 18 September 2017 (UTC) I would like to do this using this information from the FDA site on Bar Code Label Requirements^[1]TLund (talk) 23:59, 18 September 2017 (UTC)[reply]

I would like to add more information about medication administration errors and relate them to the five rights. I plan to analyze each of the rights and include information about the effects of administration error. Shilpaus76 (talk) 01:35, 22 September 2017 (UTC)shilpaus76[reply]

bibliography Guidance for Industry: Bar Code Label Requirements.(2006). Retrieved from http://www.fda.gov/biologicsbloodvaccines/guidancecomplianceregulartoyinformation/guidances/default/htm TLund (talk) 16:53, 22 September 2017 (UTC) Department of Health and Human Services: Food and Drug Administration, Bar Code Label Requirements for Human Drug Products and Biological Product; Final Rule. (2004) Retrieved from http://www.gpo.gov/fdsys/pkg/FR-2004-2-26/pdf/04-4249.pdf TLund (talk) 16:53, 22 September 2017 (UTC)[reply]

I made the changes listed above to the main page, I would appreciate some feed back on the changes, Thank youTLund (talk) 19:28, 2 November 2017 (UTC)[reply]

References

^ U.S. Food and Drug Admistration https://www.fda.gov/downloads/biologicsbloodvaccines/guidancecomplianceregulatoryinformation/guidances/ucm267392.pdf. Retrieved 18 September 2017. {{cite web}}: Missing or empty |title= (help)

[1] U.S. Food and Drug Admistration https://www.fda.gov/downloads/biologicsbloodvaccines/guidancecomplianceregulatoryinformation/guidances/ucm267392.pdf. Retrieved 18 September 2017. {{cite web}}: Missing or empty |title= (help)

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