Creating, Selecting and Positioning of Fair Balance in HCP drug advertising Dannie Newman PAAB Reviewer

Slides:



Advertisements
Similar presentations
FD 16.0 FORMULA APPROVAL POLICY 2011 Lets Get The Changes Started.
Advertisements

An Overview of Direct-to-Consumer Prescription Drug Promotion Nancy M. Ostrove, Ph.D. Risk Communication Advisory Committee May 15, 2008.
Management of Drug Formulary Dimitry Gotlinsky Western University Managed Care Clerkship ProPharma Pharmaceutical Consultants, Inc. 06/16/06.
Interactive Drug Search Application Tutorial All Content ©2006 Health Alliance Plan.
Evidence Based Advertising “Don’t accept your dog’s admiration as conclusive evidence that you are wonderful” -Ann Landers.
@ PMCQ October 14, Agenda l PAAB info l Common Review Issues l Current Initiatives l Trends.
Health Care Claim Preparation & Transmission Chapter 8 OT 232 Lecture 2 1OT 232 Ch 8 lecture 1.
Preventive Ethics Beyond the Basics. Module 3 Describing Best Ethics Practice.
@ PMCQ U October 19, Agenda l What is Advertising? l Pre-Launch Activities You Can Do l PAAB pre-NOC Meeting/Review policy.
Morning Wrap-Up. Submissions: – Make sure all the “T” are crossed and “I” are dotted – this will prevent delays – Be clear about functionality – Identify.
Medication Guides Nancy M. Ostrove, Ph.D. Division of Drug Marketing, Advertising, and Communications.
Exploring APS categories Malika Ladha PAAB Reviewer Exploring product branded advertising vs. editorial advertising vs. corporate advertising.
Writing Reports and Proposals Chapter 14. Composing reports and proposals  Introduction  States the purpose for the report  Overviews the main idea.
RAC Study Group Chapter 16
MSU HealthTeam Michigan State University WHAT’S NEW IN 9.2.
MSU HealthTeam Michigan State University WHAT’S NEW IN 9.2.
Preclearance Procedure & Operations Helpful pointers about the submission process 1 Dannie Newman PAAB Reviewer
Objectives Why we need DHCPL Situations that call for a DHCPL Definitions DHCPL itself–content, presentation, process Target audience Current and future.
Promoting Excellence in Family Medicine Enabling Patients to Access Electronic Health Records Guidance for Health Professionals.
Medication Reconciliation Veterans Affairs North Texas Health Care System March 2008.
FDA MedWatch and Patient Safety. Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006  The Act defines a ‘serious adverse event’
Direct-to-Consumer Advertising of Prescription Drugs: Looking Back, Looking Forward Kathryn J. Aikin, Ph.D. Division of Drug Marketing, Advertising and.
Overview of the New Content and Format Requirements for Prescription Drug Labeling.
1 Lotronex ® (alosetron HCl) Tablets Risk-Benefit Issues Victor F. C. Raczkowski, M.D. Director, Division of Gastrointestinal and Coagulation Drug Products.
© 2009 Hogan & Hartson LLP. All rights reserved. Meredith Manning Partner May 20, 2009 FDA’s Internet Ad Warnings: Implications for Social Media National.
How to Obtain Institutional Review Board (IRB) Approval Richard Wagner Associate Director UCSF Human Research Protection Program August 14, 2008.
An Update on NSAID Labeling and Data Review DSaRM Advisory Committee February 10, 2006 Sharon Hertz, M.D. Deputy Director Division of Anesthesia, Analgesia,
1 FDA DRAFT GUIDANCE FOR INDUSTRY REVISED Stuart E Coleman Promotional Review and Regulatory March 30 th, 2015.
Tennessee Comprehensive Assessment Program Alternative
Slide 1 Long-Term Care (LTC) Collaborative PIP: Medication Review Tuesday, October 29, 2013 Presenter: Christi Melendez, RN, CPHQ Associate Director, PIP.
Planning and Integrating Curriculum: Unit 4, Key Topic 1http://facultyinitiative.wested.org/1.
Newspaper Design.
Social Innovation Fund Creating an Application in eGrants Technical Assistance Call 1 – 2:00 p.m. Eastern Time on Friday, March 19, ;
© 2012 Cengage Learning. All Rights Reserved. May not be scanned, copied, duplicated, or posted to a publicly accessible website, in whole or in part.
Module 3 Risk Analysis and its Components. Risk Analysis ● WTO SPS agreement puts emphasis on sound science ● Risk analysis = integrated mechanism to.
Using Medicines Safely (2:50) Click here to launch video Click here to download print activity.
Applying design modules - New TeraText design modules.
DIVISION OF REPRODUCTIVE AND UROLOGIC PRODUCTS Physician Labeling Rule Lisa Soule, M.D.
History of Pediatric Labeling
The Conceptual Framework: What It Is and How It Works Linda Bradley, James Madison University Monica Minor, NCATE April 2008.
Evidence Based Advertising Part II Beyond the TMA: From clinical trials to real world evidence.
Compliant Connections in an Increasingly Connected Population Connecting platforms into one campaign.
Evidence Based Advertising Part I Using the TMA as evidence in HCP advertising.
Creating, Selecting and Positioning of Fair Balance in HCP drug advertising Malika Ladha PAAB Reviewer
Labeling and Electronic Initiatives Rachel E. Behrman M.D., M.P.H. Deputy Director, Office of Medical Policy CDER FDA Science Board, April 15, 2005.
General Regulatory Issues in the Development of Drugs Intended for Treatment of Chronic Illness Sharon Hertz, M.D. Medical Officer Division of Anesthetic,
Advertising, APS categories and target audiences Dannie Newman Reviewer
Update on Current FDA Labeling Initiatives Iris P. Masucci, PharmD, BCPS Center for Drug Evaluation and Research FDA November 16, 2006 Pediatric Advisory.
Patient Information Dannie Newman PAAB Reviewer.
Preclearance Procedure & Operations Helpful pointers about the submission process 1 Dannie Newman PAAB Reviewer
PowerPoint Template Instructions – delete this slide! Fill in the appropriate slides. KEEP the UNDERLINED HEADINGS but change the title if instructed to.
27 June 2000Victor F. C. Raczkowski, M.D.1 Risk-Management Options Victor F. C. Raczkowski, M.D., M.S. Gastrointestinal Drugs Advisory Committee 27 June.
Prescription Drug Advertising
Promoting consumer access to affordable Prescription drugs
Non-contentious disposals
Teladoc Physician Training
Presenter: Christi Melendez, RN, CPHQ
Using Medicines Safely (2:50)
Screen & Media Statement of Attainment towards
CHAPTER 4 Information Management in Pharmacy.
9. Introduction to signal detection
Medication order entry & Fill process
Labeling and Electronic Initiatives
Screen & Media Transcript of Academic record towards Certificate III Screen & Media or CIII Screen & Media (AQF CUA31015) To edit the page contents Maintain.
PROCESS DESCRIPTIONS INSTRUCTIONS
Using Medicines Safely (2:50)
Curriculum 2.0: Standards-Based Grading and reporting
For Nurses and healthcare providers
Module 4: The Highlights!
Common Rule Updates Tips and Tricks
Presentation transcript:

Creating, Selecting and Positioning of Fair Balance in HCP drug advertising Dannie Newman PAAB Reviewer

Fair Balance Fair Balance in the PAAB code Creating the three levels of fair balance Selecting the level of fair balance Positioning fair balance

Fair Balance In alignment with section 9.1 of the Food and Drugs Act, the PAAB Code sections 2.1, 2.4, 3.5 and 7.3 require that risk information be: – Presented within the APS among the claims (s2.1.2) – APS must reflect an attitude of caution (s2.4) – Emphasis only on positive features of a drug while ignoring negative findings is not acceptable (s3.5) – Comprised of content type and quantity which adequately balances the claims – Accurate, Clear, Prominent

PAAB code Rx&D requested that the PI (Product Information) be replaced with a link to the Product Monograph A committee of industry experts convened on how to meet the above requirements in the context of changes to PAAB code s7.3 New PAAB code took effect on July 1, 2013 Guidance documents created to assist in implementing the code changes

Guidance Documents

Creating the three levels of Fair Balance

Creating Fair Balance There are 3 levels of FB: See the guidance document “Guidance on Generating the Three Base Fair balance Levels” on the PAAB website Highest Middle Lowest Decreased comprehensive- ness Note: when highest level FB is required, PAAB allows option to use middle FB within an APS to direct HCP elsewhere within the same media for highest level FB.

Constructing the Highest Level of base Fair Balance Copy Framework:

Indications and Clinical Use: Must appear verbatim at least once in the APS (s2.10.2), among or prior to first set of marketing benefit claims (s2.10.1) Don’t need to repeat the indication (change section heading) Contraindications: Include all contraindications except those which are standard across all products (i.e. allergy to product or ingredient/packaging Separate bullet points Constructing the Highest Level of base Fair Balance

Most Serious Warnings & Precautions: Summary of emphasized W&P from PM (e.g. bolded, boxed, all-caps, underlined, or described as "serious" or equivalent) are described. Bolded topic followed by description of the warning Secondary Malignancies: The following secondary malignancies have occurred, cutaneous squamous cell carcinoma, new primary melanomas and non-cutaneous malignancy. Each risk description is separated by a white space Constructing the Highest Level of base Fair Balance

Other relevant warnings & precautions: Only need to include the topic, not a description (point is to identify the W&P, directing the HCP to the TMA for more information) Separate bullet point for each individual warning Can be grouped together if done so in TMA or if considered to be adequately descriptive Be sure to identify if warning is in patients with a preexisting condition, or if it is a side effect of the drug Constructing the Highest Level of base Fair Balance

For more information: Direct reader to complete TMA (link) for information not included in the fair balance Must include link to the current TMA Documents are available upon request through a stated phone number Example: For More Information: Please consult the product monograph at for important information relating to adverse reactions, drug interactions, and dosing information which have not been discussed in this piece. The product monograph is also available by calling us at XXX-XXXX

What can the link lead to? Page housing TMA on the product website Product Information page on the Health Canada Drug Product Database Directly to a PDF of the TMA on the corporate page bdpp/info.do?code=86588&lang=eng ucts/products/monograph/317

Tips for Highest level fair balance There is no need to include content relating to indications which are not promoted in the APS Content may be summarized provided the complete essence is captured. No need to repeat info presented elsewhere in the APS (section heading should reflect not complete) – Manufacturers may still elect to spread fair balance throughout the APS. Risk elements which are bolded/boxed in the product monograph are not required to be bolded/boxed in the fair balance presentation: Some content can be omitted at the manufacturer’s discretion: – See page 11 appendix in guidance document for content that can be removed from FB Constructing the Highest Level of base Fair Balance

Appendix from the Supplement: Guidance on Generating the Three Fair Balance Levels The following can be removed from the Fair Balance copy (at the discretion of the Advertiser): Content which applies to all categories of drugs irrespective of therapeutic area – e.g. contraindications in patients with known allergies to the product or its ingredients – e.g. only use in those who are pregnant/nursing where benefits exceed risk Instructions which are covered by standards of practice for all drugs – e.g. instruct patients to keep out of reach of children – e.g. only physicians who are knowledgeable with the product or class should prescribe Copy which has been presented elsewhere in the advertisement/APS Copy which is promotional

The following can be removed from the Fair Balance copy (at the discretion of the Advertiser): Copy describing risks which have not been demonstrated to be associated with the product – e.g. Product was shown not be associated with weight gain Copy about alternative therapeutic options in case of adverse effects on the advertisers product – E.g. Dietary restrictions on Brand X may not extend to other products in the class, another product within the class maybe tried with caution Explanations why the product is contraindicated in certain populations Medical definitions and thresholds (except if within the indication statement) Appendix from the Supplement: Guidance on Generating the Three Fair Balance Levels

Indication Revised

Constructing the Middle Level of Fair Balance Copy Framework Indication statement unless stated elsewhere in the APS, e.g. Headline Consult the Product Monograph at for important information on: Contraindications in… Most serious warnings and precautions… Other relevant warnings and precautions… Conditions of clinical use, adverse reactions, drug interactions and dosing instructions The product monograph is also available by calling us at xxx-xxxx.

FAMILAZE acts by inhibiting prostaglandin synthesis Familaze (rulomine hydrochloride) is indicated for the management of chronic pain associated with osteoarthritis (OA) of the knee  Inhibits prostaglandin G/H synthase isoenzymes  Also know as COX-1 and COX-2 (p<0.01)* Middle Level of Fair Balance Consult the product monograph at for important information about:  Contraindications in patients with urinary retention, gastric retention, uncontrolled narrow-angle glaucoma, hypersensitivity to tolterodine L-tartrate, soya, peanuts, lactose.  Relevant warnings and precautions regarding increased heart rate, interaction with potent CYP3A4 inhibitors, patients at risk of gastric retention, patients at risk of urinary retention, patients with impaired hepatic function, angioedema, patients with myasthenia gravis, patients with controlled narrow-angle glaucoma, patients with impaired renal function, and use of contraception in women of childbearing potential.  Conditions of clinical use, adverse reactions, drug interactions, and dosing instructions. The Product Monograph is also available by calling us at

Constructing the Lowest Level of Fair Balance Indication statement unless stated elsewhere in the APS Consult the Product Monograph at for important information on contraindications, warnings, precautions, adverse reactions, interactions, dosing and conditions of clinical use. The Product Monograph is also available by calling us at xxx-xxxx.

Selecting the level of Fair Balance

Dependent on the type of claims in the APS Selecting Fair Balance Level: Highest Middle Lowest Decreased comprehensive- ness Therapeutic claims Pharmacologic claims No pharmacologic claims

Selecting Fair Balance Level: Highest level required if APS contains any of the following: Therapeutic claim (e.g. efficacy, safety, tolerability) Compliance/adherence claim Place in therapy claim (e.g. 1 st line treatment) Pharmacoeconomic claim Beneficial aspects of risk/burden profile from TMA If not (aside from indication), go to next slide…

Middle level required if APS contains any of the following: Pharmacologic claims other than any of those listed on prior slide (e.g. pharmacokinetics/pharmacodynamic), Presentations describing predefined measured endpoints from clinical trials without disclosing results (e.g. ongoing studies) If not (aside from indication), go to next slide… Selecting Fair Balance Level:

Lowest level required if APS contains any of the following: non-pharmacologic claims healthcare product messages other than marketing benefit claims (e.g. cautionary content) messages which do not relate to the healthcare product (e.g. disease information) Selecting Fair Balance Level:

Examples of non-pharmacological claims –market positioning/experience claims –Tablet characteristics/sensory characteristics (i.e. taste/smell) –cost comparisons –cosmetic/packaging/device characteristics –study characteristics without mention of endpoints (e.g. “largest published RCT in diabetes”) –plea to choose/prescribe the product or plea to write “do not substitute” if physician wants to ensure patient receives brand X –claims relating to instructions for use, dosage and or administration information (whether comparative or non-comparative) provided the claim does not allude, in any way, to topics discussed in slide 1 If not, consider whether exempt per s6.6. If unsure submit for an opinion.

How the drug interacts with the body in a therapeutic way How the drug interacts with the body in a non-clinical way Claims that don’t relate to an interaction between the product and the body None of the above? Is this piece exempt (s6.6)?

Testing your FB knowledge Which level of FB would you choose? 1)The first and only once-daily antihypertensive therapy 2)A new dose delivery system. Demonstrated safety profile 3)For patients with irritable bowel syndrome NOTE: If after a trial of 2 weeks, patient continues to experience similar side effects and no greater efficacy than previous therapy, continued use should be reassessed. 4)New Rizaren Tablet for ulcerative colitis Rizaren tablets have microgranules that provide predictable, uniform drug release and delivery. L H L M

Positioning of Fair Balance

Risk information should be where the claims are (meaning in the same parts of the APS). Risk information should be accorded a degree of prominence which is similar to the claim content.

Positioning of Fair Balance Indication statement – Must appear verbatim in the APS (s2.10.2) – Must appear prior to or among the first set of marketing benefit claims (s2.10.1) A statement that is designed to promote the sale of a health product It often promotes a specific product attribute

Positioning of Fair Balance General Requirements: – Fair balance should be visually comparable to body copy – Factors to consider in assessing prominence: type size (at least 75% of body copy) spacing duration, pace contrast/shade Readability location

General Requirements – Fair balance should generally not be presented below product logos (+/- tagline), references, legal mice type and/or footnotes – These elements tend to mark the end of the advertising message portion on a surface Positioning of Fair Balance

Corporate signoff Footnotes Product logo

Positioning of Fair Balance Middle to Highest level fair balance When highest level of fair balance is required you have the option to use middle fair balance direct the reader to the highest level fair balance

Linking Middle to Highest Fair Balance : The highest fair balance must be within the same tool (or directly attached to it) AND in the same media. – pull out the dosing ruler to reveal the highest fair balance. – electronic banner ad directs reader to click a link which takes him/her directly to the highest fair balance. The middle fair balance must lead directly to highest level fair balance. Access to the highest fair balance should require little to no effort in day- to-day use of the piece. Surface must be easy to read

Middle fair balance must be: Within the main advertising message Wording must be adjusted to reflect language directing to the highest level fair balance Linking Middle to Highest Fair Balance :

40 High Level of Fair Balance

Middle Level of Fair Balance 41

… with High Level Fair Balance Option

Positioning of Fair Balance Linear tools vs. non-linear tools Websites – Safety information should appear on homepage/surface – Safety information tab in menu items which is accessible from all screens (links to highest level of fair balance)

Consider fair balance and indication positioning in: – a print detail aid – an Positioning of Fair Balance

Example: Sample Holder exterior side surface

Example: Dosing Slide-out Ruler

Summary of Fair Balance How to create the three levels of fair balance How to select the level of fair balance required based on the claims in the APS Where to position the fair balance copy in the APS Any questions??