CHOLESTEROL DRUGS – – a DEATH SENTENCE?

CHOLESTEROL DRUGS – – A DEATH SENTENCE? Coenzyme Q10 — also called ubiquinone, which means “occurring everywhere” — plays an important role in the manufacture of ATP, the fuel that runs cellular processes. Though it is present in every cell in your body, it is especially concentrated in the very active cells of your heart. Depriving the heart of CoQ10 is like removing a spark plug from your engine — it just won’t work. Low levels of CoQ10 are implicated in virtually all cardiovascular diseases, including angina, hypertension, cardiomyopathy and congestive heart failure. WHAT IS MERCK WAITING FOR? Merck knew that statins deplete CoQ10, and knew that this could contribute to heart disease. In 1990, this drug manufacturer sought and received a patent for Mevacor and other statin drugs formulated with up to 1,000 mg of coenzyme Q10 to prevent or alleviate cardiomyopathy, a serious condition that can cause congestive heart failure. However, Merck has not brought these combination products to market, nor has this drug company educated physicians on the important of supplementing CoQ10 to offset the dangers of these drugs to the heart.

Because they hold the patent, other drug companies are prevented from coming out with a statin/CoQ10 product. If you’re taking a statin drug (Zocor, Provacol, etc.), don’t wait for your doctor to warn you of the substantial risks. Consider this fact: in the last 15 years (roughly the time that statins have been on the market), the incidence of congestive heart failure has tripled. If you want to avoid becoming a statistic, it is imperative that you take 200 mg of coenzyme Q10 daily. You should also try to lower your cholesterol levels with a low-fat diet, targeted nutritional supplements and exercise. Statin drugs cost a bundle and are dangerous. An inexpensive alternative works better for most people. The cost is almost nothing. This may reduce or eliminate your reliance on cholesterol-lowering medication. I dumped Zocor a year ago. My cholesterol is 185 and, better yet, the HDL/LDL ratio is better than when on Zocor. Please read the article before beginning.

Which Supplements Are The Best And Which Are Just Hype? A good question but one that lacks a definitive answer. I take vitamin and mineral supplements. Can I say with certainty that they keep me healthy? I don’t know. I’m rarely sick. Maybe I’ll have a cold for a couple of days every few years. Is that because of the vitamins and supplements or is it genetic? My dad was rarely sick as well and I don’t think he took any supplements. Also if you do a little research, there are conflicting studies on just about every supplement out there as to whether we need them or not. I found it hard to find a consensus except that unless your doctor prescribes something for you, you should try to get most of your vitamins and minerals from the food you eat. How Are Supplements Regulated? You should know the following if you are considering using a dietary supplement.

Federal law requires that every dietary supplement be labeled as such, either with the term “dietary supplement” or with a term that substitutes a description of the product’s dietary ingredient(s) for the word “dietary” (e.g., “herbal supplement” or “calcium supplement”). Federal law does not require dietary supplements to be proven safe to FDA’s satisfaction before they are marketed. For most claims made in the labeling of dietary supplements, the law does not require the manufacturer or seller to prove to FDA’s satisfaction that the claim is accurate or truthful before it appears on the product. In general, FDA’s role with a dietary supplement product begins after the product enters the marketplace. That is usually the agency’s first opportunity to take action against a product that presents a significant or unreasonable risk of illness or injury, or that is otherwise adulterated or misbranded. Dietary supplement advertising, including ads broadcast on radio and television, falls under the jurisdiction of the Federal Trade Commission.

Once a dietary supplement is on the market, FDA has certain safety monitoring responsibilities. These include monitoring mandatory reporting of serious adverse events by dietary supplement firms and voluntary adverse event reporting by consumers and health care professionals. As its resources permit, FDA also reviews product labels and other product information, such as package inserts, accompanying literature, and Internet promotion. Dietary supplement firms must report to FDA any serious adverse events that are reported to them by consumers or health care professionals. Dietary supplement manufacturers do not have to get the agency’s approval before producing or selling these products. It is not legal to market a dietary supplement product as a treatment or cure for a specific disease, or to alleviate the symptoms of a disease. To check out more information on Experienced Coenzyme Q10 supplier stop by the internet site. There are limitations to FDA oversight of claims in dietary supplement labeling. For example, FDA reviews substantiation for claims as resources permit. Well, that certainly makes me feel safe and warm, how bout you? Having said all that about how the FDA regulates our supplements, I do take some vitamins and supplements that I’ve researched and feel comfortable taking.

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