The Food and Drug Administration (FDA) announced the tentative approval of Lamivudine Tablets manufactured by Aurobindo Pharma LTD. Hyderabad, India. This product will now be available for consideration for purchase under the President?s Emergency Plan for AIDS Relief (PEPFAR).
The Food and Drug Administration (FDA) announced the tentative approval of two applications for nevirapine tablets manufactured by Ranbaxy Laboratories Limited, Guragon, India and Aurobindo Pharma Limited, Hyderabad, India. These are the first generic versions of Viramune Tablets manufactured by Boehringer Ingelheim. These products will now be available for consideration for purchase under the President?s Emergency Plan for AIDS Relief (PEPFAR).
New research under the direction of Paul Khavari, MD, PhD, professor in the Program in Epithelial Biology at the Stanford University School of Medicine and chief of the dermatology service at the Veterans Affairs Palo Alto Healthcare System, shows a novel and more effective way of testing which mutations cause cancer and which are mere research distractions. The work is published in the June issue of Nature Genetics.
A drug that curbs appetite has been found to reduce a host of factors that contribute to type 2 diabetes – including elevated blood sugar levels, a study has shown.
A study found rituximab to be a safe and effective treatment for rheumatoid arthritis. The U.K. study, which included 465 men and women who had had arthritis for about 10 years, examined the effects of two doses of the drug.
The cancer drug rituximab may benefit lupus patients with central nervous system (CNS) complications, according to a new U.S. study.
An experimental pill that controls blood fats as well as blood sugar could be a better treatment for diabetics with high cholesterol even though side effects may be worse than current drugs, researchers said.
The Food and Drug Administration (FDA) approved a new vaccine for a single booster immunization against pertussis (whooping cough), in combination with tetanus and diphtheria, for adolescents and adults 11-64 years of age. The vaccine will be marketed as Adacel by Aventis Pasteur Limited located in Toronto, Canada. Adacel is the first vaccine approved as a pertussis booster for adults. Vaccines for prevention of tetanus and diphtheria (Td vaccine) in adolescents and adults have been available for many years.
School-based programmes that develop individual young people’s social skills are the best way to reduce drug use.
The low affinity glutamate NMDA receptor antagonist memantine can slightly reduce deterioration in patients with moderate to severe Alzheimer’s disease, but the effect in less severely affected people is unknown.