AbbVie: LinkedIn ‘like’ ruled promotion of unlicensed Durysta (AUTH/3493/3/21)

📅 2021 | 🖉 Dr Anzal Qurbain
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Key facts

Case numberAUTH/3493/3/21
CompanyAbbVie Limited
ProductDurysta (sustained release bimatoprost implant)
ChannelLinkedIn (employee ‘liked’ a third-party post)
Main issuePromotion of an unlicensed medicine / pre-authorisation promotion via social media engagement
ComplainantContactable complainant
Complaint received22 March 2021
Case completed10 January 2022
Applicable Code year2019
Breach clausesClause 2; Clause 3.1; Clause 9.1
SanctionsUndertaking received; Advertisement
AppealNo appeal

Download the full case report (PDF)


Reviewed by Dr Anzal Qurbain (FFPM) — ABPI Final Signatory

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What happened

  • A complainant provided screenshots alleging a named senior UK employee of AbbVie had promoted Durysta (sustained release bimatoprost implant) on LinkedIn.
  • The employee ‘liked’ a LinkedIn post by a US eye surgeon celebrating first use of Durysta after FDA approval.
  • The post named Durysta, referenced its indication (glaucoma/eye pressure) and included promotional claims (eg “no pain”, “no restrictions”, “new era for our patients”).
  • AbbVie said the individual was employed by Allergan at the time (during integration following AbbVie’s acquisition of Allergan) but functionally reporting into AbbVie; AbbVie responded.
  • AbbVie stated there was no pending UK/EU marketing authorisation application at the time of its response; the Panel still considered Durysta unlicensed in the UK.
  • The Panel considered that ‘liking’ increases the likelihood content is shown to one’s connections (ie proactive dissemination) and that the employee had 500+ connections likely including HCPs/decision makers and members of the public, predominantly in the UK.
  • The Panel noted AbbVie’s policy warned against endorsing third-party statements, but did not clearly address ‘liking’ and its dissemination effect.
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Outcome

  • Breach of Clause 3.1 ruled (promotion of a medicine prior to the grant of its marketing authorisation).
  • Breach of Clause 9.1 ruled (high standards not maintained).
  • Breach of Clause 2 ruled (bringing discredit upon, and reducing confidence in, the pharmaceutical industry).
  • No appeal.
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