Pharmaceutical behemoth Pfizer has reached agreements in principle to resolve substantially all of the personal injury and consumer fraud cases and state attorneys general claims involving its COX-2 inhibitor non-steroidal anti-inflammatory pain drug Bextra (valdecoxib), which was voluntarily withdrawn from the US market in 2005. This was a year after fellow US drug major Merck & Co pulled its COX-2 drug Vioxx (rofecoxib) due to adverse events reported with the drug, and triggered an avalanche of law suits against the company as well as questions about similar compounds (Marketletters passim).
Additionally, following key court rulings in favor of Pfizer's Celebrex (celecoxib), claims regarding the latter, an effective pain treatment for millions of patients, will also be resolved as part of the settlement, Pfizer adds.
"We are pleased by the favorable rulings we have achieved in this litigation and believe that now is the right time to resolve these matters," said Amy Schulman, senior vice president and general counsel of Pfizer. "Inevitably, litigation can be distracting and putting these matters behind us helps our shareholders and, most importantly, patients and doctors," she noted.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze