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Cancer drug reverses transplant rejection: study (AFP)
A drug used to treat cancer has proven effective at stopping the body from rejecting a transplanted organ when other treatments failed, a study published Saturday found.
yahoo.com

FDA Approves Latisse For Hypotrichosis Treatment
The U.S. Food and Drug Administration (FDA) has approved LATISSE (bimatoprost ophthalmic solution) 0.03% as a novel treatment for hypotrichosis of the eyelashes. Eyelash hypotrichosis is another name for having inadequate or not enough eyelashes. LATISSE is the first and only FDA-approved, science-based treatment to enhance eyelash prominence as measured by increases in length, thickness and darkness of eyelashes.read more
CBC.ca

Attention to bones important in women with lupus
Among premenopausal women taking steroids for lupus, varioustreatments preserve bone mineral density and 'should be considered'for preventing the bone-thinning disease osteoporosis, adviseresearchers in a report published this month.
Cholesterol Network

FDA Requires Additional Data For Seroquel XR Supplemental New Drug Application
The U.S. FDA (Food and Drug Administration) has asked AstraZeneca, the makers of Seroquel XR (quetiapine fumarate), for additional information for its extended release tablets for the treatment of MDD (Major Depressive Disorder) in adult patients. The FDA's CRL (Complete Response Letter) was sent to AstraZeneca on 24th December. AstraZeneca says it is evaluating the contents of the letter and the proposed labeling revisions.
Medicalnewstoday.com

Phase III Study Showed Rituxan® Decreased The Progression Of Joint Damage In Patients With Early Rheumatoid Arthritis (RA)
Genentech, Inc. (NYSE: DNA) and Biogen Idec (Nasdaq: BIIB) announced that a Phase III clinical study of Rituxan® (rituximab) in patients with early rheumatoid arthritis (RA) who have not previously been treated with methotrexate (MTX) met its primary endpoint. In this study, known as IMAGE, patients received two infusions of either 500 mg or 1000 mg of Rituxan or placebo for up to two treatment courses in combination with a stable dose of MTX.
Medicalnewstoday.com

Multiple Courses Of Antenatal Steroids Do Not Improve Preterm Birth Outcomes And Can Lead To Decreased Baby Size (Macs Study)
Multiple courses of antenatal corticosteroids, every 14 days, do not improve outcomes for premature babies are associated with a decreased baby weight, length, and head circumference at birth. Therefore this treatment schedule is not recommended. These are conclusions of the MACS study, reported in an Article in The Lancet, written by Dr Kellie E Murphy, Department of Obstetrics and Gynaecology Mount Sinai hospital, Toronto, Canada and colleagues from the MACS Collaborative Group.
medicalnewstoday.com

Glivec Receives US Approval As First Treatment To Reduce Risk Of Cancer Returning In Patients With Gastrointestinal Stromal Tumors
Novartis announced that Glivec® (imatinib) has been approved by the US Food and Drug Administration (FDA) for the post-surgery treatment of adult patients following complete surgical removal of Kit (CD117)-positive gastrointestinal stromal tumors (GIST). Glivec is now the only post-surgery treatment indicated to delay the return of this highly aggressive cancer, filling a major need for GIST patients.
Medicalnewstoday.com

MabThera Inhibits The Destruction Of Joints In Patients With Early Rheumatoid Arthritis
Roche announced recently that MabThera (rituximab) can significantly inhibit structural damage to joints in patients with early rheumatoid arthritis (RA) who have not been treated with methotrexate (MTX), the current standard of care for RA treatment.
Medicalnewstoday.com

Frostbite Treatment and Prevention: FAQ
Title: Frostbite Treatment and Prevention: FAQCategory: Health NewsCreated: 12/26/2008Last Editorial Review: 12/26/2008
CBC.ca

Failed by the NHS: 82,000 deprived of dental treatment
MORE than 82,000 people in Scotland are stuck on waiting lists to get access to an NHS dentist, figures obtained by The Scotsman have revealed.
Jointogether.org

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