Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Chapter 3 Drug Regulation, Development, Names, and Information.

Slides:



Advertisements
Similar presentations
Consumer Safety and Drug Regulations
Advertisements

Clinical Trials Medical Interventions
Chapter 4 Cultural, Legal, and Ethical Considerations Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
Pharmacology Application in Athletic Training Michelle Odai, MS, LAT, ATC, CSCS Florida International University.
FEDERAL REGULATIONS OF MEDICATIONS Food, Drug and Cosmetic Act Protect consumers from adulterated and misbranded foods, drugs, cosmetics, or devices.
Pharmacology Ch 4-9. Drug Controls Federal Food & Drug Act – 1906 Federal Food & Drug Act – 1906 Required identification of dangerous or addictive drugs.
© 2006 McGraw-Hill Higher Education. All rights reserved. Chapter 3 Drug Products and Their Regulation.
Pharmaceutical Development and Review Process Rev. 10/21/2014 APGO Interaction with Industry: A Medical Student Guide.
INVESTIGATIONAL DRUG SERVICES IN THE HOSPITAL Sheree Miller, Pharm.D. University of Washington Medical Center
Mosby items and derived items © 2007 by Mosby, Inc., an affiliate of Elsevier Inc. Chapter 4 Prescription Writing.
Stages of drug development
Mosby items and derived items © 2007 by Mosby, Inc., an affiliate of Elsevier Inc. Chapter 1 Information, Sources, and Regulatory Agencies.
Mosby items and derived items © 2008, 2002 by Mosby, Inc., an affiliate of Elsevier Inc. Chapter 1 Introduction to Respiratory Care Pharmacology.
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 3 Drug Regulation, Development, Names, and Information.
Eureka Pre-Clinical Investigation Animal toxicology Animal pharmacokinetics/ pharmacodynamics Clinical Investigation Phase I Safety and pharmacology Phase.
Principles of Pharmacology
Chapter 1: Information, Sources, Regulatory Agencies, Drug Legislation, and Prescription Writing Copyright © 2011, 2007 Mosby, Inc., an affiliate of Elsevier.
1 Copyright © 2011, 2007, 2003, 1999 by Saunders, an imprint of Elsevier Inc. All rights reserved. Chapter 2 Pharmacy Law, Standards and Ethics for Technicians.
Testing People Scientifically.  Clinical trials are research studies in which people help doctors and researchers find ways to improve health care. Each.
Copyright C 2005, 2002, 1999, 1995, 1990, 1985, 1980, 1976 by Elsevier Inc. Principles of Pharmacology Chapter 30.
Federal Laws CHAPTER 3. DRUG REGULATION Timeline highlights –Food Drug & Cosmetic (FDC) Act –Durham Humphrey Amendment –Poison Prevention Packaging Act.
Investigational Drugs in the hospital. + What is Investigational Drug? Investigational or experimental drugs are new drugs that have not yet been approved.
Mosby items and derived items © 2010, 2007, 2004 by Mosby, Inc., an affiliate of Elsevier Inc. Definitions, Names, Standards, and Informational Sources.
Copyright (c) The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 9-1 Chapter 9 Principles of Pharmacology.
1 Chapter 2 Drug Classes, Schedules, and Categories.
© 2004 by Thomson Delmar Learning, a part of the Thomson Corporation. Fundamentals of Pharmacology for Veterinary Technicians Chapter 1 A Brief History.
© 2004 by Thomson Delmar Learning, a part of the Thomson Corporation Fundamentals of Pharmacology for Veterinary Technicians 1 Submitted by Callie Parr.
Orientation to Pharmacology
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 2 Application of Pharmacology in Nursing Practice.
© 2009 McGraw-Hill Higher Education. All rights reserved. Drug Products and Their Regulations.
Using Medicines Safely (2:50) Click here to launch video Click here to download print activity.
© 2009 McGraw-Hill Higher Education. All rights reserved. Drug Products and Their Regulations.
© 2011 McGraw-Hill Higher Education. All rights reserved. Chapter 3 Drug Products and Their Regulations.
Mosby items and derived items © 2007, 2005, 2002 by Mosby, Inc., an affiliate of Elsevier Inc. CHAPTER 4 Cultural, Legal, and Ethical Considerations.
The New Drug Development Process (www. fda. gov/cder/handbook/develop
The FDA: Basic Facts It takes 12 to 15 years to develop a single drug Only 1 in 10,000 potential medications makes it completely through the process Only.
Copyright © 2010 Delmar, Cengage Learning. ALL RIGHTS RESERVED. Chapter 35 Basic Pharmacology.
Copyright © 2010 Delmar, Cengage Learning. ALL RIGHTS RESERVED. Chapter 23 and 24 Basic Pharmacology Medication Calculations Dosage.
Focus on Nursing Pharmacology
Pharmacology Fundamentals
Mosby items and derived items © 2005, 2002 by Mosby, Inc. CHAPTER 4 Legal, Ethical, and Cultural Considerations NDEG 26 A – Pharmacology 1 Eliza Rivera-Mitu,
Drug Regulation, Development, Names, and Information Chapter 3 Copyright (c) 2004 Elsevier Inc. All rights reserved.
Jamie Bango Lindsey Croker Kristen Lantz Achidi Ndiforchu.
Chapter 2 The Drug Approval Process Copyright © 2015, 2012, 2009, 2006, 2003, 2000, 1997, 1993 by Saunders, an imprint of Elsevier Inc.
Copyright © 2013 by Saunders, an imprint of Elsevier Inc. All rights reserved. Chapter 6 Drug Information References.
(c) 2005 The McGraw-Hill Companies, Inc. All rights reserved. Chapter Eighteen: Becoming an Informed Health-Care Consumer.
Section I General principle of Pharmacology. Where can you get information about general principle of Pharmacology?  Text books:  Katzung, Basic and.
Meet & Greet. Welcome Objectives: 1. Review the core terminology used in pharmacology. 2. Discuss the features of the “perfect” drug. 3. Examine the.
Clinical Trials.
Chapter 2 Drug Names and References. Back in the Game Sports Medicine is a clinic dedicated to the treatment of physical injuries to the body. Caring.
Drug Use, Regulation, and the Law Chapter 3. Guidelines for Controlling Drug Development and Marketing Society has the right to protect itself from the.
Pharmacology Science that studies interactions of drugs with organism on different levels (subcellular, cellular, organ, systemic) Studies: - relationship.
Copyright © 2016 by Mosby, an imprint of Elsevier Inc.
1 Introduction to Pharmacology.
Clinical Trials Medical Interventions
Chapter 2 Medication Development Regulations and Resources
Clinical use of PAH drugs based on functional class
Using Medicines Safely (2:50)
Bozeman Health Clinical Research
The Nursing Process and Pharmacology Jeanelle F. Jimenez RN, BSN, CCRN
Cultural, Legal, and Ethical Considerations
Clinical Trials.
Introduction to Pharmacology: Drug Regulation and Approval Chapter 1
Orientation to Pharmacology
Speeding access to therapies
The Different Phases Of Clinical Trials
Pharmacy practice experience I
Chapter 35 Basic Pharmacology.
Using Medicines Safely (2:50)
Prescriptive Authority for Nurse-Midwives in Georgia
Presentation transcript:

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Chapter 3 Drug Regulation, Development, Names, and Information

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Landmark Drug Legislation  Federal Pure Food and Drug Act, 1906  Food, Drug, and Cosmetic Act, 1938  Harris-Kefauver Amendments, 1962 (Thalidomide response)  Controlled Substances Act, 1970  Permission for accelerated drug approval,

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Landmark Drug Legislation (Cont.)  Prescription Drug User Fee Act, 1992  Food and Drug Administration Modernization Act, 1997  Best Pharmaceuticals for Children Act, 2002  Pediatric Research Equity Act, 2003  FDA Amendments Act, 2007 (after the drug has been approved)  Family Smoking Prevention and Tobacco Control Act,

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. New Drug Development  The randomized controlled trial  Use of controls  Randomization  Blinding 4

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Stages of New Drug Development  Preclinical testing  Clinical testing  Phase I  Phases II and III  Phase IV: Postmarketing surveillance 5

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Limitations of the Testing Procedure  Limited information about the majority of people:  Women  Children  Failure to detect all adverse effects 6

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Exercising Discretion Regarding New Drugs  Be neither the first to adopt the new nor the last to abandon the old  Balance potential benefits against inherent risks  New drugs generally present greater risks than old ones 7

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Drug Names Chemical name Generic name Trade name The three types of drug names: 8

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Which Name to Use: Generic or Trade?  Use of drug names  Written and oral communication about medicines  Labeling medication containers 9

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Which Name to Use: Generic or Trade?  The little problems with generic names  More complicated than trade names  The big problems with trade names  Single drug can have multiple trade names  U.S. drugs and drugs outside the United States may have different active ingredients  Products with the same trade name may have different active ingredients For example, Kaopectate 10

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. 11

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Which Name to Use: Generic or Trade?  Generic products vs. brand-name products  Are generic products and brand-name products therapeutically equivalent?  Would a difference between brand-name and generic products justify the use of trade names? 12

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Over-the-Counter Drugs  Americans spend about $20 billion annually on over-the-counter (OTC) drugs  OTC drugs account for 60% of all doses administered  Forty percent of Americans take at least one OTC drug every 2 days  Four times as many illnesses are treated by a consumer using an OTC drug as by a consumer visiting a physician 13

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Over-the-Counter Drugs (Cont.)  For most illnesses (60% to 95%), initial therapy consists of self-care, including self- medication with an OTC drug 14

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Sources of Drug Information  People  Clinicians and pharmacists  Poison control centers  Pharmaceutical sales representatives 15

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Published Information  Reference books  Goodman & Gilman’s The Pharmacological Basis of Therapeutics  Pharmacotherapy: A Pathophysiologic Approach  Applied Therapeutics: The Clinical Use of Drugs 16

Copyright © 2016, 2013, 2010 by Saunders, an imprint of Elsevier Inc. All rights reserved. Published Information  Newsletters  The Medical Letter on Drugs and Therapeutics  Prescriber’s Letter  Reference books  Physicians’ Desk Reference  Drug Facts and Comparisons  Nursing drug references  The Internet 17