Posts Tagged ‘drugs’

www.encognitive.com AMERICAN SCIENTISTS SAY THEY INVENTED A CURE FOR HEART DISEASE IN 1991 According to one of the world’s most highly regarded scientists , we human beings no longer have to fear premature death or heart attack caused by progressive cardiovascular disease (CVD), undergo heart by-pass surgery or angioplasty, or suffer the chest pain of Angina Pectoris. The medicinal substances involved are not drugs. The two primary ingredients of the Linus Pauling invention are both required in some daily amount for life itself. The great benefit comes from taking these two completely non-toxic substances in amounts much larger than one normally consumes in the diet. Linus Pauling did not make this claim lightly, although he made it without fanfare. Pauling waited until after careful experiments at his institute confirmed the Lp(a) C connection. The details of this amazing discovery, its suppression by medical authorities, elements of the United States government and other governments, and the mainstream press, are described on these web pages. You can also view a Linus Pauling lecture on video tape. Pauling explains how you can return your cardiovascular health, safely, without surgery. Thanks to medical science, it is now possible for cardiovascular disease patients to live a more healthful future; free of pain and symptoms of their former cardiovascular illness. An extraordinary claim. A claim unknown to most doctors, but one those suffering severe disease can verify …

FDA has received about 30 reports of sudden hearing loss in patients taking a class of erectile dysfunction drugs called PDE5 inhibitors. This class of drugs includes Viagra (sildenafil), Cialis (tadalafil) and Levitra (vardenafil). The problem was sometimes accompanied by tinnitus, vertigo, or dizziness. In most cases the hearing loss involved one ear, and about a third of the time it was temporary. Medical follow-up information was often limited for the reported cases, which makes it difficult to determine whether these reports are directly related to the use of one of these drugs, an underlying medical condition, or other risk factors for hearing loss, a combination of these factors, or other factors. FDA has asked the manufacturers of these erectile dysfunction drugs to display the risk of hearing loss more prominently in the labeling, and to guide patients on what to do if they experience hearing problems while they are on the drugs. The revised label will advise clinicians to let patients know that sudden hearing loss may be due to the drug, and to stop taking the drug and seek medical attention if they experience any sudden decrease or loss of hearing. Another PDE5 inhibitor, Revatio, also contains sildenafil, the same active ingredient as in Viagra. However, Revatio is used to treat pulmonary arterial hypertension rather than erectile dysfunction. FDA is working with the manufacturer of this drug to revise its labeling, too. Because pulmonary hypertension is a …

Mirtazapine was developed in the United States in 1990 to care for depression. It was approved by the Federal Drug Administration in 1996 and is thought to reduce chemical imbalances within the brain that cause depression and anxiety. It may take some time of treatment before one can get the full benefits of the medication. Usually given at bedtime, the drug may cause nausea and sleepiness. It also has other side effects that can be bothersome, such as weight gain and dizziness. However, it has been found to be one of the most successful drugs for depression and the side effects are usually short-lived and mild. When thinking about taking or purchasing this drug, Mirtazapine standards are important, so make sure you find a qualified manufacturer.

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The u . s . Food and Drug Administration will begin controlling the medications imported from foreign nations at the US borders. A trial run has already concluded in Los Angeles and will now be rolled out all across the rest of the nation, commencing in New York. The Food and drug administration hopes that by the end of the Spring the new border control will be in position nation-wide. The new plan is known as PREDICT or Predictive Risk-based Evaluation for Dynamic Import Compliance Targeting and will evaluate imported medications based on many factors. The companies and facilities will be taken into consideration. Addionally, the prescription drugs will be rated in terms of safety as well as other variables. These types of controls and in depth FDA consulting will ensure that all imported medicinal drugs going into the United states pharmaceutical market place are in line with FDA compliance.

The Food and drug administration hope that by enforcing tighter controls and inspections on imported medicines, the danger they pose to American patients will be reduced. This comes after several instances where contaminated and substandard medicines have entered the us medicine market place. Patients who took them suffered medical problems and there have even been instances of death. One instance of this was the case of contaminated Heparin which brought about hundreds of deaths around the world back in 2008. Subsequently, the Food and drug administration and the people of The united states have been much more concerned about the standard of imported medicines.

The PREDICT program will work with a barcode system. A central database will be connected to the control stations on the US borders and will hold essential information regarding a number of variables. Instantly the system will be able to warn the Food and drug administration officers if the producer of the medicinal drugs has the right permit to sell their products in America. If no such permit exists then the medications will be confiscated and destroyed.

When it comes to ranking the medications, the variables that will be taken into consideration as to their rank include the reputation of the producer, the facility that they were made at and present market conditions amongst others. The bigger|greater|larger[/spin] the risk the deeper the investigation the medications will be put through.

This plan will be operating alongside other efforts by the Food and drug administration to regulate imported medications. To ensure FDA compliance they have already established offices in India, China and Latin America. With these projects FDA consulting should increase among all producers that make medications to be used throughout the United states.

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People given beta blockers were 10 to 24 times more like to dropout of studies due to fatigue, and 5 times more like to dropout of studies due to sexual dysfunction. Beta blockers only prevent one stroke per year out of every 1400 patients given these drugs. They only prevent one heart attack per year out of every 1400 patients given these drugs. And they only prevent one death per year out of every 2500 patients given these drugs. This was noted in a Letter to the Editor in JAMA by Franz Messerli, MD who has written several papers about the ineffectiveness of beta blockers. For every one heart attack or stroke that is prevented by these drugs 3 people are made impotent 8 people have so much fatigue that they stop taking the drug. ” hardly an acceptable risk/benefit ratio for a completely asymptomatic disease such as mild essential hypertension.” — Franz Messerli, MD “In the case of hypertension in patients older than 60 years, such benefits [of beta blockers] have not been documented.” — Franz Messerli, MD In other words beta blockers have not been shown to benefit people over the age of 60. Hi, this is Larry Hobbs @ FatNews.com, Beta blockers include drug like atenolol (Tenormin) and propranolol (Inderal). I believe that potassium bicarbonate is vastly superior to beta blockers and the other blood pressure medicines for improving health. I’ve been taking 1000 mg of potassium twice a day (2000 mg per day) in the form of potassium bicarbonate since 2000. My blood …

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