We understand that all industries are regulated differently. To help pharma companies, we’ve become experts in Adverse Events. Tsvetta Kaleynska, founder of RILA GLOBAL CONSULTING explains.

It’s interesting to monitor the transition from traditional marketing to social media marketing from a behavioristic perspective.

Is social media not the way to get your daily news, communicate with loved ones and share your wittiest thoughts?

Brands have been banking seriously on consumer’s interests online, on all of your comments, likes and shares of their stories on Facebook, Twitter and a bunch of other platforms. Small and large enterprises have been creating their campaigns and strategies solely on your posts online.

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So when it comes to evaluating which brands use social insights the most, it’s quite surprising that one of the largest industries out there – pharmaceuticals – is somewhat new to social.

Their efforts to listen to their consumers online are still fresh due to the strict regulations imposed across each continent.

The FDA and Adverse Events

In recent years, the pharma companies worldwide have been better at understanding what their consumers are saying online about their products and brands. In the United States, the FDA has been strictly moderating all pharma access to social data which has ultimately reflected in a slower adoption for social across the board. The FDA refers to “adverse events” scenarios, anything posted online matching 4 criteria:

  • Identifiable patient – should contain the patient who it happened to (personal pronounces often help with that – i.e. “I got sick / My sister felt / My brother experienced.”)
  • Identifiable reporter – with robots, cyberbots etc. the FDA requires that the person who reports the message is a person and also reachable via their social handle, email, phone, etc.
  • Medication identification – should contain the specific name of the medication.
  • An adverse effect / event – the content posted online should describe an adverse or side effect the medication may have had.

So how have the FDA and adverse events hindered social listening for pharma companies?

The adverse events regulations have prevented the large pharma companies to not only listen to what customers are saying, but also to see the mentions themselves.

Social media insights platforms provide clients with all of the mentions and data there is on the topic of interest, but it turns out that pharmaceutical companies cannot actually see the individual content.

There are multiple social media solutions offering a special permission setting pharma companies are required to be compliant with the FDA.  The “view only” permission settings in social platforms allows users to extract the insights they need without being endangered by viewing the mentions themselves. All components charts are compliant with the policies implemented in the pharma space and provide users with the opportunity to tap into the data fast and safe.  

In most interfaces, you’ll find the User Role in the User Role drop-down when creating or editing a user.

Metrics User roles have similar permissions to regular permissions, however in most cases you’d encounter that:

  • Regular social listenings users cannot see any parts of setups that show mentions, or parts of mentions.
  • They cannot click through to any mentions (designed to ensure users remain “safe” and do not see any Adverse Events.)

To help our pharma clients best, RILA GLOBAL CONSULTING has become among the leading experts in Adverse Events. If you need help with social listening in the pharma space, don’t hesitate to drop us a note at tsvetta@rilaglobal.com.

*Cover Image Source: https://www.sciencenewsforstudents.org/blog/eureka-lab/test-pill-coatings-try-stomach-flask