The US Food and Drug Administration has responded to a 2011 petition from consumer rights advocacy group Public Citizen regarding certain common antacid medications.
Public Citizen petitioned for stronger warnings and patient medication guides on all proton pump inhibitor products such as Nexium (esomeprazole), Prevacid (lansoprazole) and Prilosec (omeprazole). It then sued the FDA in federal district court for unreasonable delay in responding to the petition.
In its response, which came on October 31, the FDA agreed with and granted the following requests:
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 2024 | Headless Content Management with Blaze