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ARE
YOU SUFFERING FROM A COLD OR SEASONAL ALLERGIES?
HISPANIC AMERICAN ALLERGY, ASTHMA AND IMMUNOLOGY
ASSOCIATION PROVIDES IMPORTANT INFORMATION ON THESE COMMONLY CONFUSED CONDITIONS
Bridgewater, N.J.,
March 11, 2002 – With
spring allergy season upon us, Aventis Pharmaceuticals, the maker of AllegraÒ
(fexofenadine HCl) 180 mg once daily and Allegra® 30 mg twice daily
for children 6 to 11 years of age, and the Hispanic American Allergy, Asthma and
Immunology Association (HAAMA) today launched a national education campaign,
“La Diferencia entre una Alergia y un Resfriado,” to help people distinguish
between seasonal allergy and common cold symptoms.
“I have seen an
increase in the number of Hispanic Americans who visit me about a persistent
cold when they are actually suffering from seasonal allergies,” said
Dr. Jorge Quel, allergist and Executive
Director
of HAAMA. “There is a need to raise awareness of the differences
between the common cold and seasonal allergies in order to help reduce the
current confusion that exists.”
Seasonal allergies affect more than 35 million people in
the United States. They are a
chronic condition caused by the body’s reaction to allergens such as grass and
tree pollens that enter the body through the respiratory tract.
A cold is a viral infection of the upper respiratory tract.
Physicians have many therapy
options available to treat seasonal allergies, including prescribing a
non-sedating antihistamine such
as AllegraÒ
(fexofenadine HCl) 180 mg once daily, Allegra® 30 mg twice daily for
children 6 to 11 years of age or
twice daily Allegra-D® (fexofenadine
HCl 60 mg/ pseudoephedrine
HCl 120 mg) extended-release tablets
for congestion.
About
Allegra
Allegra®
(fexofenadine HCl) 30 mg twice daily is indicated in the United States for the
relief of seasonal allergic rhinitis and chronic idiopathic urticaria (hives) in
children aged 6 to 11. Side effects
with Allegra 30 mg are low and may include headache, cold, coughing, or
accidental injury.
Allegra®
(fexofenadine HCl) 60 mg twice daily
is indicated in the United States for the
relief of seasonal allergic rhinitis in patients aged 12 and older.
Side effects with Allegra 60 mg for
seasonal allergies are low; less than 3% of people experience cold or flu,
nausea, menstrual pain or drowsiness.
Allegra® (fexofenadine HCl) 180
mg once daily is a powerful, safe and effective non-sedating antihistamine for
the treatment of seasonal allergy symptoms in patients 12 years and older.
Side effects with Allegra are low and may include headache, cold or back
pain.
Twice-daily
Allegra-D® (fexofenadine HCl 60 mg/pseudoephedrine HCl 120 mg)
extended-release tablets provide non-drowsy effective relief of seasonal allergy
symptoms, including nasal congestion. Side
effects with Allegra-D were similar to Allegra alone and may include headache,
insomnia, and nausea. Due to the
decongestant (pseudoephedrine) component in Allegra-D, this product must not be
used if you: are taking an MAO inhibitor (a medication for depression) or have
stopped taking an MAO inhibitor within 14 days; retain urine; have narrow-angle
glaucoma; have severe high blood pressure or severe heart disease.
You should tell your doctor if you have high blood pressure, diabetes,
heart disease, narrow-angle glaucoma, thyroid disease, impaired kidney function,
or symptoms of an enlarged prostate such as difficulty urinating.
Allegra
(fexofenadine HCl) is available by prescription only, and seasonal allergy
sufferers should consult their physician or health professional with questions.
Full prescribing information is available by visiting the Aventis
Pharmaceuticals U.S. Web site at www.aventispharma-us.com.
Also available at this U.S. Web site are copies of this release or any
recent release, or call 800/207-8049.
About
Aventis Pharmaceuticals
Aventis Pharmaceuticals conducts the U.S.
business of Aventis Pharma AG. With
headquarters in Bridgewater, N.J., Aventis Pharmaceuticals focuses its
activities on important therapeutic areas such as cardiology, oncology, anti-infectives,
arthritis, allergy and respiratory, diabetes, and the central nervous system.
Aventis
Pharma AG is the pharmaceutical company of Aventis S.A. (NYSE:AVE).
Aventis Pharma is dedicated to treating and preventing human disease
through the discovery, development, manufacture and sale of innovative
pharmaceutical products aimed at fulfilling unmet medical needs.
The corporate headquarters of Aventis Pharma is in Frankfurt, Germany.
Aventis Pharma is comprised of Aventis Pharmaceuticals; Aventis Pasteur, a world
leader in vaccines, headquartered in Lyon, France; and Aventis Behring, a world
leader in therapeutic proteins, headquartered in King of Prussia, Pa.
Aventis SA, a world leader in
pharmaceuticals and agriculture, is headquartered in Strasbourg, France. In 2000, Aventis generated group sales of € 22.3 billion
($20.6 billion) and employed around 92,500 people.
The company announced in November 2000 that it intends to focus on
pharmaceuticals and plans to divest it activities in agriculture.
Aventis was launched in December 1999 through the merger of Hoechst AG of
Germany and Rhône-Poulenc SA of France. For
more information, please visit: www.aventis.com.
Full prescribing information is available by
visiting the Aventis Pharmaceuticals U.S. Web site at http://www.aventispharma-us.com.
Also available at this U.S. Web site are copies of this release or any
recent release, or call 800/207-8049.
Statements in this news release other
than historical information are forward-looking statements subject to risks and
uncertainties. Actual results could
differ materially depending on factors such as the availability of resources,
the timing and effects of regulatory actions, the strength of competition, the
outcome of litigation, and the effectiveness of patent protection.
Additional information regarding risks and uncertainties is set forth in
the current Annual Report on Form 20-F of Aventis on file with the Securities
and Exchange Commission.
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