際際滷

際際滷Share a Scribd company logo

Rtcrm perspectives facebook share this function warning letter

RTC
RTC

The FDA issued a warning letter to Novartis for their "Facebook Share" functionality on the website for the drug Tasigna. The letter cited that shared posts about Tasigna omitted important risk information and broadened the approved use of the drug. This suggests the FDA considers shared social media posts to be promotional material that requires pre-clearance and balanced risk/benefit disclosures like other promotional content. Marketers must understand how social sharing tools generate messages and ensure compliance with FDA regulations to avoid enforcement actions.

1 of 1
Download to read offline
RTC Relationship Marketing Perspectives FDA Issues Facebook Share Warning Letter Michelle Fares, Interactive Strategy August 9, 2010 Summary: In a warning letter publicly posted on August 4, 2010, the FDA cited the Facebook Share functionality on Novartis Tasigna website for failing to deliver appropriate risk and efficacy information, and for failure to pre-clear the communications. This suggests that DDMAC considers Facebook Share and other content sharing technology generated messages to be promotional material, and all stakeholders must fully understand and evaluate this functionality before including it on any branded or unbranded website Key Information The FDA warning letter cites the Facebook Share functionality of Novartis Tasigna website for disseminating misleading content about the drug on Facebook. Tasigna is a second-line treatment for chronic myelogenous leukemia (CML) and carries a black box warning for severe risks. Tasignas HCP and consumer websites include a Facebook Share tool that, upon a visitors action, pulls information from the page to share on Facebook. This information makes representations about the efficacy of Tasigna but fails to communicate any risk information. The content also indicates that Tasigna is approved to treat all individuals with CML, although it is only approved as a second-line treatment for patients with chronic or accelerated CML. Furthermore, the unique messages created for the shared content were not submitted for required pre-clearance by the Division of Drug Marketing, Advertising and Communications (DDMAC). This warning indicates that the FDA considers Facebook Share content to be promotional material and requires it to be submitted to the same review process as all other promotional copy. Violations: 1. Omission of Risk Information: Facebook Share text does not mention the black box warning or any risks associated with Tasigna. The HCP-directed shared content reads: Tasigna (nilotinib) is used to treat a type of leukemia called Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML), and the consumer- directed content states: In addition to taking Tasigna (nilotinib) 200-mg capsules, talking to your doctor and receiving health tips can help you treat your CML. 2. Broadening of Indication: Shared content implies that Tasigna is used to treat all individuals with CML; however, it is only approved as a second-line treatment for chronic or accelerated CML. 3. Overstatement of Efficacy: One instance of the Facebook Share text on the consumer-directed site refers to Tasigna as a next generation treatment and implies an unproven superiority over other tyrosine kinase inhibitors that treat PH+ CML. 4. Failure to Submit: Novartis failed to submit these materials to DDMAC for approval before or at the time of publication. Implications and Action Items Because information sent through Facebook Share and other content sharing technology is now considered promotional material, it is imperative to understand how the technology generates messages and to assess the return- on-investment (ROI) before including this sharing technology on a website. Consider the appropriateness of content sharing technology: If a drugs target market is not an active user of social media or the content does not lend itself to word-of-mouth advocacy, the risks associated with implementing and managing content sharing technology may outweigh the benefits. Understand how each type of content sharing technology works: It is important to understand how each unique sharing technology being considered generates content and to vet all content as unique messages. Take note that the FDA is paying closer attention to sharing technology: Because the FDA considers this content promotional material, it is subject to the same review and management requirements as other copy. Leverage precedent: Googles adquequate provision format for pharma paid search ads can serve as a guide on how to balance risk and benefit information. Google search ads now are able to display the following: Click to see full safety and prescribing information, including black boxed warnings, at www.drug.com. To review the Novartis warning letter, please visit http://tinyurl.com/fdaletter3. For more reviews on FDA guidelines, please visit http://www.rtcrm.com/whitepapers and http://www.rtcrm.com/blogs. FDA warning letters and FDA guidelines can be found at http://www.fda.gov.

More Related Content

Rtcrm perspectives facebook share this function warning letter

  • 1. RTC Relationship Marketing Perspectives FDA Issues Facebook Share Warning Letter Michelle Fares, Interactive Strategy August 9, 2010 Summary: In a warning letter publicly posted on August 4, 2010, the FDA cited the Facebook Share functionality on Novartis Tasigna website for failing to deliver appropriate risk and efficacy information, and for failure to pre-clear the communications. This suggests that DDMAC considers Facebook Share and other content sharing technology generated messages to be promotional material, and all stakeholders must fully understand and evaluate this functionality before including it on any branded or unbranded website Key Information The FDA warning letter cites the Facebook Share functionality of Novartis Tasigna website for disseminating misleading content about the drug on Facebook. Tasigna is a second-line treatment for chronic myelogenous leukemia (CML) and carries a black box warning for severe risks. Tasignas HCP and consumer websites include a Facebook Share tool that, upon a visitors action, pulls information from the page to share on Facebook. This information makes representations about the efficacy of Tasigna but fails to communicate any risk information. The content also indicates that Tasigna is approved to treat all individuals with CML, although it is only approved as a second-line treatment for patients with chronic or accelerated CML. Furthermore, the unique messages created for the shared content were not submitted for required pre-clearance by the Division of Drug Marketing, Advertising and Communications (DDMAC). This warning indicates that the FDA considers Facebook Share content to be promotional material and requires it to be submitted to the same review process as all other promotional copy. Violations: 1. Omission of Risk Information: Facebook Share text does not mention the black box warning or any risks associated with Tasigna. The HCP-directed shared content reads: Tasigna (nilotinib) is used to treat a type of leukemia called Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML), and the consumer- directed content states: In addition to taking Tasigna (nilotinib) 200-mg capsules, talking to your doctor and receiving health tips can help you treat your CML. 2. Broadening of Indication: Shared content implies that Tasigna is used to treat all individuals with CML; however, it is only approved as a second-line treatment for chronic or accelerated CML. 3. Overstatement of Efficacy: One instance of the Facebook Share text on the consumer-directed site refers to Tasigna as a next generation treatment and implies an unproven superiority over other tyrosine kinase inhibitors that treat PH+ CML. 4. Failure to Submit: Novartis failed to submit these materials to DDMAC for approval before or at the time of publication. Implications and Action Items Because information sent through Facebook Share and other content sharing technology is now considered promotional material, it is imperative to understand how the technology generates messages and to assess the return- on-investment (ROI) before including this sharing technology on a website. Consider the appropriateness of content sharing technology: If a drugs target market is not an active user of social media or the content does not lend itself to word-of-mouth advocacy, the risks associated with implementing and managing content sharing technology may outweigh the benefits. Understand how each type of content sharing technology works: It is important to understand how each unique sharing technology being considered generates content and to vet all content as unique messages. Take note that the FDA is paying closer attention to sharing technology: Because the FDA considers this content promotional material, it is subject to the same review and management requirements as other copy. Leverage precedent: Googles adquequate provision format for pharma paid search ads can serve as a guide on how to balance risk and benefit information. Google search ads now are able to display the following: Click to see full safety and prescribing information, including black boxed warnings, at www.drug.com. To review the Novartis warning letter, please visit http://tinyurl.com/fdaletter3. For more reviews on FDA guidelines, please visit http://www.rtcrm.com/whitepapers and http://www.rtcrm.com/blogs. FDA warning letters and FDA guidelines can be found at http://www.fda.gov.