. 2007;
35:319-326.
3. Lyles KW, Colon-Emeric CS, Magaziner JS, et al. for the HORIZON
Recurrent Fracture Trial. Zoledronic acid and clinical fractures and
mortality after hip fracture. N Engl J Med. 2007:537:1799-1809.
4. National Osteoporosis Foundation. Fast Facts on Osteoporosis Brochure.
February 2008.
5. U.S. Department of Health and Human Services. Bone Health and
Osteoporosis: A Report of the Surgeon General. 2004, p. 88.
6. Zometa(R) (zoledronic acid) Injection [Prescribing Information]. East
Hanover, NJ: Novartis Pharmaceuticals Corporation. March 2008.
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Page: 1 2 3 4 5 6 7 Related medicine technology :1.
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