Zelnorm

Zelnorm Official FDA information, side effects and uses.


FDA rejections likely to raise cost to develop drugs - Houston Chronicle




FDA rejections likely to raise cost to develop drugs
Houston Chronicle, United States -Aug 17, 2007
... warnings on several drugs, most prominently diabetes drugs Avandia and Actos, and five months ago made Novartis withdraw its constipation drug, Zelnorm. ...


FDA to Allow Limited Use of Zelnorm - FDA news (subscription)

FDA to Allow Limited Use of Zelnorm
FDA news (subscription), VA -Aug 3, 2007
The FDA has decided certain patients will be able to take Novartis’ Zelnorm, despite the fact that Novartis withdrew the drug from the market at the ...


FDA to allow Zelnorm under restricted access - Pharmaceutical Business Review

FDA to allow Zelnorm under restricted access
Pharmaceutical Business Review -Jul 31, 2007
By Staff Writer The FDA is permitting a restricted access program for Novartis' irritable bowel syndrome drug Zelnorm after suspending the drug earlier this ...


Novaris and FDA Begin Treatment IND for Zelnorm - Associated Content

Novaris and FDA Begin Treatment IND for Zelnorm
Associated Content, CO -Jul 29, 2007
The program is designed to give limited access to Zelnorm to women under the age of 55 in the US "who suffer from irritable bowel syndrome with constipation ...


Zelnorm(R) to be Made Available to US Patients Under Restricted ... - PR Newswire (press release)

Zelnorm(R) to be Made Available to US Patients Under Restricted ...
PR Newswire (press release), NY -Jul 27, 2007
FDA approves limited treatment IND program for Zelnorm -- Novartis continues discussions with FDA to evaluate Zelnorm safety data and identify appropriate ...