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Statin therapy, muscle function and falls risk in community-dwelling older adults
QJM: An International Journal of Medicine
MD Linx

Americans spend $34B for alternative medicine
ATLANTA (AP) -- Americans spend more than a 10th of their out-of-pocket health care dollars on alternative medicine, according to the first national estimate of such spending in more than a decade....
Associate Press

Alternative Medicine 101
New to complementary and alternative medicine? Information to get you started.
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Statement By Merck & Co., Inc. Regarding FOSAMAX (alendronate Sodium) ...
Statement By Merck & Co., Inc. Regarding FOSAMAX And Rare Cases Of Osteonecrosis Of The Jaw Main Category: Bones / Orthopaedics Also Included In: Pharma Industry / Biotech Industry Merck is committed to putting patients first and providing accurate information regarding the efficacy, safety and tolerability of our medicines.
Topix.net

Statement By Merck & Co., Inc. Regarding FOSAMAX® (alendronate Sodium) And Rare Cases Of Osteonecrosis Of The Jaw
Merck is committed to putting patients first and providing accurate information regarding the efficacy, safety and tolerability of our medicines. Merck offers the following statement concerning the osteoporosis medication FOSAMAX® (alendronate sodium) and reports of jaw problems associated with delayed healing and infection of the jaw often following tooth extraction. (Source: Health News from Medical News Today)MedWorm Message: Get the very latest Swine Flu news via the MedWorm Swine Flu RSS news feed - updated hourly from thousands of authoritative health and news sources.
Med Worm

Regulatory Update: Mepolizumab For The Treatment Of Hypereosinophilic Syndrome (HES)
GSK announced that it has notified the European Medicines Agency of its decision to withdraw the Marketing Authorisation Application (MAA) in the EU for mepolizumab for the treatment of hypereosinophilic syndrome (HES).
Medical News Today

Merck KGaA Has Requested Re-examination Of The CHMP Opinion For Erbitux In Non-Small Cell Lung Cancer
Merck KGaA announced that it has requested re-examination of the negative opinion from the Committee for medicinal products for Human Use (CHMP), the scientific committee of the European Medicines Agency (EMEA), for the use of Erbitux® (cetuximab) in combination with platinum-based chemotherapy for the first-line treatment of patients with non-small cell lung cancer (NSCLC).
Medical News Today

Ilaris® Recommended For European Approval As New Biologic Drug To Treat A Rare But Serious Group Of Auto-inflammatory Diseases
The biotechnology medicine Ilaris® (canakinumab) has passed another major milestone with a recommendation for approval in the European Union to treat patients with a life-long and potentially fatal auto-inflammatory disease called cryopyrin-associated periodic syndrome (CAPS). When approved, Ilaris will be the only treatment in the EU indicated for CAPS patients aged four years and older[1].
Medical News Today

Unique Immunization Method Provides Insights About Protective Anti-Malaria Immune Response
In this week's New England Journal of Medicine, scientists in Singapore, The Netherlands and France report that they have developed a novel immunization method that will induce fast and effective protection in humans against the life-threatening malaria parasite, Plasmodium falciparum, which infects 350 to 500 million people world-wide and kills over one million people each year.
Medical News Today

FDA Approves Expanded Use Of ISENTRESS® (raltegravir) In Combination Therapy For Adult Patients With HIV-1 Infection
Merck & Co., Inc. announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for ISENTRESS®. The broadened indication now includes use in the treatment of adult patients starting HIV-1 therapy for the first time (treatment-naïve), as well as in treatment-experienced adult patients. ISENTRESS is used in combination with other antiretroviral (ARV) medicines for the treatment of HIV-1 infection in adult patients.
Medical News Today

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