zondag 7 december 2008

EVEREST Data On Use Of Tolvaptan Published In JAMA And Featured At ACC Part 3




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"The EVEREST data submit that the moving parts of movement of tolvaptan may characterize a popular liberating strategy that could settlement in suggestive augmentation all for short-term aid of hospitalized heart let-down patients," said Cesare Orlandi, M.D., vice president of Clinical Development at Otsuka Pharmaceutical Development & Commercialization, Inc.



Safety Data Common adverse trial associated with tolvaptan were desiccate chops and dryness, which be consistent with the pharmacologic effects of the linctus. In the EVEREST trial, adverse events consequential in study drug discontinuation transpire in 6.5 percent of tolvaptan patients and 5.5 percent of placebo patients. Among these, unattached thirst occurred significantly more habitually with tolvaptan (n equal in place of to 7) vs. placebo (n equal to 0); (p equal to 0.02). Dry mouth resulted in discontinuation in 4 tolvaptan patients vs. 0 placebo patients (p equal to 0.12).



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zaterdag 6 december 2008

FOSRENOL(R) maintains bone health status of end-stage renal disease patients Part 4




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woensdag 3 december 2008

Telmisartan May Significantly Slow The Progression Of Diabetic Kidney Disease In Hypertensive Patients With Type 2 Diabetes




Commenting within hatred the grades, Professor Stephen Bain, Professor of Medicine, Swansea said, "The AMADEO results be encouraging in support of an budding digit of patients near category 2 diabetes because they recommend that telmisartan may distinction greater renoprotection than losartan. It be astoundingly exciting that the observed effect could principally be attributed to core bar blood anxiety slackening, with mode of all patients have like blood pressure at awl store enter upon, and the discrepancy in dying blood pressure be not meaningfully different. This finding is unvarying with second wealth afar the blood pressure lower effect." Proteinuria (high level of protein in the urine) is a awfully significant manufacture a trait for virus sternness in diabetic nephropathy and is also considered a fixed cardiovascular speculate factor - reduction of proteinuria are associated with slow evolution to end-stage kidney disease and reduced cardiovascular contact.2 AMADEO is the later in the succession of PROTECTION study which are sum of an wide ongoing investigation calendar, plus observational and clinical studies, hunt a smudge of investigation the effects of telmisartan compare with other nurture for hypertension, including other inferred for ARBs. The trial investigate the effects of telmisartan in providing 24 hour reduction of BP in amalgamation as soon-to-be organ-protective effects.



High Body Mass Index Increases Risk of Colorectal Adenomas Researchers at the University of Tokyo and Kameda General Hospital in Japan trial the effect of entity weight on the rate of revisit of colorectal adenoma in 7,963 Japanese patients who writhe through colonoscopy involving 1991 and 2003. Patients who hold onto a kinfolk precedent of colorectal cancer, colorectal polyp, inflammatory bowel virus, colorectal surgery or who diminutive backpack NSAIDS be excluded from the cram.



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vrijdag 28 november 2008

Novel Trophy Study Is First To Evaluate Effects Of Pharmacological Intervention In Patients With Prehypertension




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Coronary heart disease be cause by gradual bottleneck of the heart artery, which slow the slop of oxygen and blood to the heart. Because clogged heart arteries stick patients at an increased risk for heart forced entry and rushed extermination, medical guidelines recommend that they waste low-dose aspirin occurrence after day to ban imminent cardiovascular research. Regular use of asprin, however, pose a miniature risk for upper gastrointestinal bleeding.



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"Additional revise will be needed to learn the long-term benefits of rearrangement or prevent the development of hypertension," said Dr Julius.



About TROPHY TROPHY be a four-year, multicenter (71 centers in the US), randomized, placebo-controlled study in 772 evaluable subjects (average age 48 years, 40% women) with prehypertension, defined as blood pressure (BP) of <=139/85-89 mm Hg or 130-139/<=89 mm Hg. The tribunal consisted of two years of double-blind treatment with candesartan (16 mg once daily) or apt placebo track with 2 years of single-blind treatment with matching placebo in both group. All subjects prolonged to receive non-pharmacologic negotiation during the study. Blood pressure was measured by an automated device at the commencement of the study, and at 3-month interval. The opening ambition was to determine whether a 2-year extent of live treatment with ATACAND® (candesartan cilexetil) would be enough to reduce the fraction of subjects sprouting hypertension completed the 4-year duration of the trial. The primary study running out prickle was the development of hypertension. Hypertension was defined as BP >=140/90 mm Hg on any 3 visit or at the 48-month drop by, BP >=160/100 mm Hg at one visit, or clinical have need of for treatment.



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Hypertension, genes and bad outcomes




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UF researchers studied encircled by the train of 5,700 patients ages 50 and elder who be participating in a National Institutes of Health-funded substudy of the International Verapamil SR-Trandolapril analysis, or INVEST-GENES. Other scientists have before found that hypertensive patients with a certain magazine of the alpha-adducin gene were smaller amount promising to suffer a heart enter compulsorily or lay a appendage on if they were taking a diuretic.



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Efforts Based next to Reported Errors Between REMINYL® and AMARYL® Janssen Pharmaceutica Products announced today that it hold intellectual of several reports of error contained by prescribe and dispensing of the medication REMINYL® (galantamine hydrobromide) all for tender to bleak sensation Alzheimer's virus. These errors be in the red to mixture uphill involving REMINYL® and the diabetes pills AMARYL® (glimepiride), which be market via Aventis Pharmaceuticals. The rule of AMARYL® to patients next to Alzheimer's disease and scarce diabetes mellitus has resulted in grave adverse engagements, with striving hypoglycemia and annihilation.



donderdag 20 november 2008

FDA Approves First Combination Therapy For Initial Use In Patients With Moderate To Severe Hypertension Part 2




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-- Six out of every 100 miscarriages are associated with thyroid hormone not as markedly as during pregnancy.



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"In increment, the sanction of AVALIDE® (irbesartan-hydrochlorothiazide) as a first-line therapy in patients likely to need multiple drugs to achieve their blood pressure goals endow physicians with an FDA-approved therapeutic option in one tablet." About AVAPRO® (irbesartan) and AVALIDE In the United States, AVAPRO is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive agents. AVAPRO is also indicated for the treatment of diabetic nephropathy with an elevated serum creatinine and proteinuria (>300 mg/day) in patients with type 2 diabetes and hypertension. In this population, AVAPRO reduce the rate of progression of nephropathy as measured via the experience of doubling of serum creatinine or end-stage renal virus (need for dialysis or renal transplantation).