Pharmaceutical companies can obtain many benefits from listening to social media. But, explains Dr. Ed Tucker of Janssen Research & Development, a Johnson & Johnson company, in such a highly regulated industry, more active engagements need to be carefully conducted.

Dr. Ed Tucker is vice president and head of pharmacovigilance operations, Global Medical Safety for Janssen Research & Development LLC, which is part of Janssen Pharmaceuticals, a Johnson and Johnson subsidiary. Janssen Pharmaceuticals itself produces pharmaceuticals for treating a wide range of diseases and disorders, including ADHD, gastroesophageal reflux disease, bipolar I disorder, schizophrenia, Alzheimer’s disease, epilepsy, pain management and a variety of other health concerns.

Tucker’s role at Janssen is to gather safety-related data to inform his company — and government regulators — about patient use of its products. His department sends Individual Case Safety Reports to national government regulatory agencies about adverse events experienced by patients using Janssen’s products, whether in clinical trials, physician-prescribed therapy, or over-the-counter purchases. Thus, it is important to his function that he communicates with patients about their use of pharmaceuticals.

Social media provides a new platform and opportunity for connecting with patients and learning about their safety concerns, questions or comments, and presents new opportunities for collecting key information. However, in such a highly regulated and sensitive area as pharmaceuticals, there needs to be extra care and vigilance in how such information is gathered, including an awareness of the legal requirements about reporting certain safety-related data.

In this interview, Tucker describes how social media is providing new opportunities in his own role as well as some of its promise for the pharmaceutical industry as a whole, and how the industry can take advantage of the potential of social media without violating safety, privacy and other regulatory restrictions.

How important is the social media business to your organization right now and what are some special challenges given your industry?

It is very important. In pharmacovigilance, we receive a lot of safety information that gives us insight into our products and the patients receiving our products. We are often one of the downstream recipients of information from other parts of the company that engage in social media activities.

One of the unintended consequences for a pharma company entering the digital media space is triggering certain regulatory requirements around the reporting of safety information.

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2 Comments On: How Pharmaceuticals Can Avoid the Side Effects of Social Media

  • siva.nadarajah | April 16, 2013

    Here at Semantelli, we are seeing an uptick in activity from pharma companies in listening and engaging in social media. Our AETracker software and 24/7 Social Media Adverse Event Command Center helps pharma companies listen and engage in social media minimizing regulatory risks.

    Siva Nadarajah
    CEO, Semantelli Corp.
    http://www.semantelli.com/pharma

  • Sven Awege | April 23, 2013

    Great insights shared by Dr Tucker – clearly with a big slant on the pharmacovigilance hat on. Pharma can benefit from Social Media in many additional ways if we think it through carefully. Patient safety and risk management is important, but other areas to consider could be better design of clinical studies (if we know what the real concerns are we might define better primary objectives…), measuring the impact of disease awareness campaigns (are we actually changing behavior), KOL identification….
    All exciting stuff.
    Thanks again.

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