GlaxoSmithKline Consumer Healthcare, Cephalon UK Ltd and ProStraken Group plc have been named and publicly shamed for breaching the Association of the British Pharmaceutical Industry's (ABPI) Code of Practice.
GlaxoSmithKline Consumer Healthcare, Cephalon UK Ltd and ProStraken Group plc have been named and publicly shamed for breaching the Association of the British Pharmaceutical Industry’s (ABPI) Code of Practice. The code covers the promotion of medicines, including journal and direct mail advertisements, and the provision of information to patients and the public.
The companies have breached the code in different ways; however, all three stand in violation of Clause 2 of the code: bringing discredit upon and reducing confidence in the pharmaceutical industry, according to a statement released by the Prescription Medicines Code of Practice Authority (PMCPA), which administers the ABPI Code of Practice.
GlaxoSmithKline Consumer Healthcare
The case against the pharma giant stems from the company making misleading claims about its smoking cessation aid NiQuitin. The complaint was made by Johnson & Johnson after the company received a mailing promoting the product. The mailing contained the claim “From day one NiQuitin 25mg Clear Patch delivers more nicotine than any other therapeutic nicotine patch”, which was alleged by Johnson and Johnson to be “ambiguous and misleading” primarily because of a lack of clarity relating to the measures of speed and the extent of nicotine delivery upon which the claim was based.
In response, the PMCPA ruled that the company was in breach of Clause 2, as well as other clauses relating to:
Cephalon
Cephalon breached the code by providing free stock of its breakthrough pain treatment, Effentora (a Schedule 2 controlled drug that is subject to ordering/storage and prescribing restrictions) without “sufficient controls”. According to the code, no more than 10 free samples should be provided but in this instance the company supplied 30. The complaint also attached emails that stated Effentora was supplied as an inducement to prescribe and “assist [Cephalon] with moving forward with a formulary application”.
Despite an appeal, Cephalon was ruled as breaching Clause 2, as well as further clauses relating to failing to maintain high standards.
ProStrakan
ProStrakan’s breach of the code stemmed from the company making claims about its Abstral that were misleading and did not comply with a previous undertaking. In a previous case (case number: AUTH/2207/2/09), the PMCPA had ruled that a “10 minute pain relief claim” of Abstral was in breach of the code as the product only provided pain relief from 15 minutes after administration onwards. The most recent case draws from a complaint made by Cephalon. According to the company, a revised promotional campaign for Abstral inferred that the product was actually even faster in onset than 10 minutes by using the advertisement heading ‘To hell and back in minutes’.
The ABPI’s Prescription Medicines Code of Practice Authority (PMCPA) has advertised brief details of all cases in the BMJ and The Pharmaceutical Journal on 21 August, and in The Nursing Standard on 25 August. The full case reports have been published in the PMCPA’s August Code of Practice Review.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.