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Treatment of inflammatory and autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis and multiple sclerosis.
On April 28, 2011, the US Food and Drug Administration (FDA) approved Zytiga (abiraterone acetate), for use in combination with prednisone for the second-line treatment of castration-resistant prost...
The iBioLaunch™ platform is a proprietary gene expression technology that causes non-transgenic plants to rapidly produce high levels of target proteins. The plants are easily and ...
Veregen® is an ointment used to treat external genital warts. In the USA, Germany, Austria, Spain, Switzerland and Serbia, Veregen® is already marketed by our partners. Sales and marketing p...
The Ras-Raf-MEK-ERK (ERK) pathway is a logical therapeutic target because it represents a common downstream pathway for several key growth factor tyrosine kinase receptors which are often mutated or...
Kentucky has filed a lawsuit against Johnson & Johnson’s medical device unit, Ethicon, alleging it concealed and purposely misrepresented the risks involved in its surgical transvaginal mesh pr...
Commentary on a study comparing low-cost mesh with commercial mesh for the repair of inguinal hernias, published in the New England Journal of Medicine. Medscape General Surgery
A New York federal judge has ruled in favor of Bayer AG against nearly 1,300 lawsuits filed by women who say they suffered internal injuries from the company's Mirena intra-uterine contraceptive d...
A judge speaks frankly about what he plans to do if lawyers keep pressing questionable vaginal-mesh cases.
Current practices do not eliminate human papillomavirus (HPV) from probes used for transvaginal ultrasound, researchers report. Reuters Health Information
NEW YORK, May 24 (Reuters) - California has accused Johnson & Johnson of failing to warn doctors and patients about the severity and frequency of complications associated with its pelvic mesh devices....
The attorney generals of California and Washington filed lawsuits alleging the company failed to disclose risks to consumers.
The plastic mesh is used to treat pelvic organ prolapse. In response to thousands of injuries from the mesh, the Food and Drug Administration early this year re-labeled the products high risk instead ...
To update clinical practice guidelines on graft and mesh use in transvaginal pelvic organ prolapse repair based on systematic review.
To identify litigation predictors among women with complications of transvaginal mesh.
To measure the proportion of women with transvaginal prolapse mesh complications and their association with surgeon volume.
To investigate long-term outcomes after transvaginal mesh repair among patients with pelvic organ prolapse in different age groups.
The objective of this study is to compare direct costs of repairing pelvic organ prolapse by laparoscopic sacrocolpopexy (LS) against vaginal mesh (VM). Our hypothesis is the correction of pelvic orga...