In clinical trials, the most common adverse reactions in > or = 2% of
adult and adolescent patients (12 years of age and older) taking XYZAL 2.5
mg, XYZAL(R) 5 mg, or placebo were somnolence (5%, 6%, 2%), nasopharyngitis
(6%, 4%, 3%), fatigue (1%, 4%, 2%), dry mouth (3%, 2%, 1%), and pharyngitis
(2%, 1%, 1%), respectively.
In clinical trials 4 to 6 weeks in duration, the most common adverse
reactions in > or = 2% of pediatric patients (6-12 years of age) taking
XYZAL(R) 5 mg included pyrexia (4% vs 2% placebo), cough (3% vs <1%
placebo), somnolence (3% vs <1% placebo) and epistaxis (2% vs <1% placebo).
Full prescribing information for XYZAL(R) is available at
http://www.XYZAL.com.
About UCB
UCB, Brussels, Belgium (http://www.ucb-group.com) is a global leader in the
biopharmaceutical industry dedicated to the research, development and
commercialisation of innovative pharmaceutical and biotechnology products
in the fields of central nervous system disorders, allergy/respiratory
diseases, immune and inflammatory disorders and oncology. UCB focuses on
securing a leading position in severe disease categories. Employing more
than 10,000 people in over 40 countries, UCB achieved revenue of 3.5
billion euro in 2006 on a pro forma basis.
About sanofi-aventis
Sanofi-aventis, a leading global pharmaceutical company, discovers,
develops and distributes therapeutic solutions to improve the lives of
everyone. Sanofi-aventis is listed in Paris (EURONEXT: SAN) and in New York
(NYSE: SNY).
UCB Forward-Looking Statement
This news release contains forward-looking statements that involve
risks and uncertainties
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SOURCE sanofi-aventis Copyright©2008 PR Newswire. All rights reserved | |
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