The U.S. Food and Drug Administration approved a second test to screen blood, tissue and organ donors for a blood-borne parasite, Trypanosoma cruzi (T. cruzi), that causes Chagas disease, a serious and potentially fatal parasitic infection. The test, called Abbott Prism Chagas [Trypanosoma...
Health News Florida: "Calling the current system 'broken' and warning of long-term financial problems, the state House today approved a proposal that would gradually shift almost all Medicaid recipients into managed-care plans. The votes on two bills set the stage for the House and Senate to try...
Health News Florida: "Calling the current system 'broken' and warning of long-term financial problems, the state House today approved a proposal that would gradually shift almost all Medicaid recipients into managed-care plans. The votes on two bills set the stage for the House and Senate to try...
Emerging World Pharma Inc. (PINKSHEETS: EWPI) president, Brandon Keks, confirmed today that the company has approved an ongoing investment allocation into European Global Pharma. The first allotment of funding has been set aside as the company completes its due diligence. "We do not anticipate...
OSI Pharmaceuticals, Inc. (NASDAQ: OSIP) announced today that the U.S. Food and Drug Administration (FDA) approved the daily pill Tarceva® (erlotinib) as a maintenance treatment for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) whose disease has not progressed...
After three days of turbulent meetings, the Texas Board of Education on Friday approved a social studies curriculum that will put a conservative stamp on history and economics textbooks, stressing the superiority of American capitalism, questioning the Founding Fathers' commitment to a purely...
After three days of turbulent meetings, the Texas Board of Education on Friday approved a social studies curriculum that will put a conservative stamp on history and economics textbooks, stressing the superiority of American capitalism, questioning the Founding Fathers' commitment to a purely...
The West Virginia House Health and Human Resources Committee on Monday voted 16-9 to approve a bill (HB 4517) that would require physicians to give women the opportunity to view an ultrasound image at least one hour before performing an abortion, the Charleston Gazette reports. According to the...
The West Virginia House Health and Human Resources Committee on Monday voted 16-9 to approve a bill (HB 4517) that would require physicians to give women the opportunity to view an ultrasound image at least one hour before performing an abortion, the Charleston Gazette reports. According to the...
The Spanish Senate on Wednesday passed a bill that would ease Spain's strict restrictions on legal abortion and instead allow the procedure up to 14 weeks' gestation without restrictions and up to 22 weeks' gestation in limited cases, the AP/Yahoo News reports. The bill also permits 16- and...
The U.S. Food and Drug Administration has approved velaglucerase alfa for injection (VPRIV) to treat children and adults with a form of the rare genetic disorder Gaucher disease. Gaucher disease occurs in people who do not produce enough of an enzyme called glucocerebrosidase. Without this...
The U.S. Food and Drug Administration has approved velaglucerase alfa for injection (VPRIV) to treat children and adults with a form of the rare genetic disorder Gaucher disease. Gaucher disease occurs in people who do not produce enough of an enzyme called glucocerebrosidase. Without this...
The Virginia Senate on Tuesday voted 26-8 to approve a bill (SB 18) that would create a specialty license plate with the message, "Trust Women. Respect Choice," and direct a portion of the revenue to the Virginia League for Planned Parenthood, the Washington Post reports. The bill also would...
Daiichi Sankyo, Inc. announced that the U.S. Food and Drug Administration (FDA) has approved the hypertension treatment Benicar® (olmesartan medoxomil) for use in children and adolescents 6 to 16 years of age.(1) Benicar was originally approved in 2002 for the treatment of hypertension in...
The Centers for Medicare & Medicaid Services (CMS) is designating three national accreditation organizations - the American College of Radiology (ACR), the Intersocietal Accreditation Commission (IAC), and The Joint Commission (TJC) - to accredit suppliers furnishing the technical component (TC)...
The Kentucky Senate on Monday voted 32-4 to approve a bill (SB 38) that would require physicians to show women an ultrasound and describe "the dimensions of the embryo or fetus and the presence of external members and internal organs, if present and viewable," the Louisville Courier-Journal...
The U.S. Food and Drug Administration approved Ampyra (dalfampridine) extended release tablets to improve walking in patients with multiple sclerosis (MS). In clinical trials, patients treated with Ampyra had faster walking speeds than those treated with an inactive pill (placebo). This is the...
The U.S. Food and Drug Administration approved Ampyra (dalfampridine) extended release tablets to improve walking in patients with multiple sclerosis (MS). In clinical trials, patients treated with Ampyra had faster walking speeds than those treated with an inactive pill (placebo). This is the...
Health Canada has approved Zyclara™ (imiquimod) Cream 3.75%, a topical prescription treatment for multiple actinic keratoses (AK) located on the face or balding scalp in adults. Actinic Keratosis is a common skin condition that can lead to squamous cell carcinoma, a form of non-melanoma skin...
The National Institutes of Health announced approval of embryonic stem cell lines for federally funded research. The Washington Post reports the decision is "opening the way for millions of taxpayer dollars to be used to conduct research that was put off-limits by President George W. Bush...