health

Instructions

1. FAERS (April 2015)FDA Drug Info Rounds pharmacists provide some background information about the FAERS databasehttps://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm442182.htm2. NDC Directory (March 2015)FDA Drug Info Rounds pharmacists discuss changes to the online National Drug Code (or NDC) Directory.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm437472.htm3. REMS (February 2015) FDA Drug Info Rounds pharmacists discuss the many components of Risk Evaluation and Mitigation Strategies (REMS) and how they can help manage a drug product with known or potential serious risks.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm433705.htm4. USP Salt Policy (December 2014)FDA Drug Info Rounds pharmacists discuss the application of the United States Pharmacopeias Monograph Naming Policy for Salt Drug Substances in Drug Products and Compounded Preparations.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm425653.htm5. Expanded Access (October 2014) FDA Drug Info Rounds pharmacists discuss expanded access to investigational drugs.https://www.youtube.com/results?search_query=Expanded+Access+%28October+2014%296. Traveling with Prescription Medications (August 2014) FDA Drug Info Rounds pharmacists discuss key points pharmacists should counsel their patients on prior to travelhttps://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm410051.htm7. Managing Drug Shortages (July 2014) FDA Drug Info Rounds pharmacists discuss the management of drug shortages and how the FDAs role has changed in recent years.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm400243.htmElectronic Orange Book (March 2014)  .Electronic Orange Book (March 2014) 8. FDA Drug Info Rounds pharmacists discuss how to search the Electronic Orange Book for generic equivalents, patents, and exclusivity.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm388798.htm9. Drug Promotion (October 2013)FDA Drug Info Rounds pharmacists discuss the many elements surrounding the marketing and advertising of a prescription drug product.https://www.youtube.com/watch?v=4hc-yiK_JIY10. Drug Name Review (September 2013)FDA Drug Info Rounds pharmacists discuss FDAs responsibility for reviewing and approving new product nameshttps://www.youtube.com/watch?v=bpRuAXVKWDI11. Communicating Benefit and Risk Information (August 2013) FDA Drug Info Rounds pharmacists talk about the benefit risk balance, and how health care professionals may approach this topic with their patients.https://www.youtube.com/watch?v=cad4TYyFjNE12. Drug Safety Communications (November 2012)FDA Drug Info Rounds pharmacists discuss how Drug Safety Communications let health care providers, patients, and consumers know about newly observed potential risks of FDA-approved drugs.https://www.youtube.com/watch?v=AUqGa9fwSAQ13. Distribution of Medication Guides (October 2012)FDA Drug Info Rounds pharmacists discuss the requirements for providing Medication Guideshttps://www.youtube.com/watch?v=zFp9oO5zI_014. Medication Errors (September 2012) FDA Drug Info Rounds pharmacists discuss Medication Errors and how FDA educates the public about medication error prevention through public health advisories, medication guides and outreach partnerships with other organizations.https://www.youtube.com/watch?v=Ux5dv2-PtBI15. Patents and Exclusivity (August 2012)FDA Drug Info Rounds pharmacists discuss Patents and Exclusivity and how they work in a similar fashion but are distinctly different from one another. Patents and Exclusivity (August 2012)16. Accelerated Approval Program (July 2012)FDA Drug Info Rounds pharmacists discuss the Accelerated Approval Program and how FDA helps make new, potentially lifesaving drugs available more quickly. https://www.youtube.com/watch?v=fzlePvW-Dg417. Disposal of Unused Medicines (January 2015) FDA Drug Info Rounds pharmacists discuss medication disposal options.https://www.fda.gov/Drugs/ResourcesForYou/HealthProfessionals/ucm429508.htmEach video contains from 2 to 4 min.After watching each video need to summarise video, discuss what you learned after watching

Answer

HEALTHQuestion 1Some background information on FAERS include the reports that have been submitted to the FDA on medical errors and adverse events. The reports submitted are purposely meant for conducting medical watch. The information is provided for identifying the safety measures and concerns that are related to marketed drugs. The reports can be received from healthcare professionals and consumers. Question 2When a drug has been assigned an NDC number, it does not mean that it will in any way donate FDA approval to the product. The changes made in NDC directory include the labeler code, where the segment may contain four or five digits. Also, there is the product code where there are three or four digits, and there is the package code which has one or two numbers.Question 3REMS is made...

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