quarter with revenues totaling $1.2 billion, an increase of 13
percent, reflecting strong double-digit sales growth across all product
categories. Driving this performance was robust growth from several
products used for the treatment of hemophilia and immune disorders,
including ADVATE [Antihemophilic Factor (Recombinant), Plasma/Albumin-Free
Method (rAHF-PFM)] and immune globulin intravenous (IGIV), as well as solid
growth from other plasma-based therapies, biosurgery products and vaccines.
Medication Delivery sales grew 8 percent in the quarter to $1.1
billion, with strong global sales of intravenous and nutritional therapies,
and significant growth in international sales of anesthesia products and
injectable drugs. Renal sales increased 6 percent to $558 million.
Baxter's investment in research and development of $190 million
increased 19 percent in the first quarter as the company continues to
advance its product pipeline across its business portfolio.
"Our strong and improving financial position reflects the continuing
momentum in our business," said Robert L. Parkinson, Jr., chairman and
chief executive officer. "Our favorable outlook for the full year allows us
to continue to accelerate our investments in research and development
programs that will improve treatment for patients, expand access to care
and enhance the quality of life for people around the world."
Since the beginning of the year, Baxter has achieved a number of
commercial, clinical and regulatory milestones, including:
-- U.S. Food and Drug Administration (FDA) approval of ARTISS [Fibrin
Sealant (Human)], the first and only slow-setting fibrin sealant
indicated for use in adhering skin grafts in adult and pediatric burn
patients.
-- The launch of GELFOAM (R) Plus Hemostasis Kit (absorbable gelatin
sponge, USP and human thrombin), which is indicated as a hemostatic
device for surgical procedures when c
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SOURCE Baxter International Inc. Copyright©2008 PR Newswire. All rights reserved | |
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