Keywords: wyeth, withdraws, duract, due, serious, liver, events
Wyeth Withdraws Duract Due To Serious Liver Events
Article | 24 June 1998
Wyeth-Ayerst Laboratories, a subsidiary of American Home Products, hasvoluntarily withdrawn its prescription non-steroidal anti-inflammatory drug Duract (bromfenac sodium capsules) from ...
Enjoying this article? To continue reading you need to login or subscribe.
Subscribe now
for unlimited access to all articles
Subscriptions are £60 per month, pay as you go.
Find out more details.
Already a subscriber? Click here to log in
- US FDA advisory panel backs approval of Merck & Co's suvorexant, but only at lower doses
- Alchemia and Merck Serono collaborate on HA-Irinotecan with Erbitux
- AstraZeneca's naloxegol meets endpoints; EMA validates Gilead's sofosbuvir MAA
- Boehringer Ingelheim gets FDA warning letter on cGMP failures
- Italy's pharma market slump set to continue, warns GlobalData
