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"A NATURAL ENVIRONMENTAL HEALTH FACTS Ezine"  Here to Inform and Help You Become Healthier and Happier while Achieving Quality Longevity!

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=> IN THIS ISSUE!
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==> Editors' Ranting & or Warnings
==> Something To Think About
==> Health Thought for the day!
==> Showcase Health Spotlight
==> Monthly Spotlight Ads
==> Today's Health Tip
==> Health Today
==> Environmental Report
==> Life Changing Information



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EDITORS' RANTING
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Greetings and thank you for being an optin subscriber!

Week flew by with the holiday and then former President Ford's funeral really making for fast and short... Did you get a chance to take assessment of your health habits? If not don't wait any longer and do what you need to be the best you can be, health wise... Have a good weekend but make sure you relax so your body can repair!

 Free evaluation and ongoing followup - free- simply email the doctor and list your info to help with that assessment ie; gender, weight, age, type of food you prefer, symptoms/diagnosis and list of all medications or over-the-counter medications as well as any nutritional supplements you take...

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Lena

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Something To Think About
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Really Good Question?

Which is More Dangerous to Your Health? the Flu or the FDA?
December 21, 2006
By John W. Whitehead


The flu season is here once again. During the last flu season, doctors reportedly wrote more prescriptions for the drug Tamiflu than any other flu treatment. But after recent reports about the Food and Drug Administration's reluctance to issue a warning about certain possible dangers of using Tamiflu, one has to wonder which is more dangerous-the flu or the FDA?

First approved by the FDA in 1999, Tamiflu was touted as a drug that could significantly reduce the length and severity of influenza. These claims even prompted the U.S. government to purchase 20 million doses of Tamiflu-at a cost of $2 billion-in the event that a bird flu pandemic occurred. The Pentagon followed, paying a whopping $58 million in July 2005 for treatments of U.S. troops around the world.

However, problems with Tamiflu began to surface in 2004. It was thought that the drug, which has been used by over 30 million people worldwide, was causing some of its users to manifest very unusual behavior. For example, during the 2004 and 2005 flu seasons, two teenage boys committed suicide within hours of taking Tamiflu. The 17-year-old jumped in front of a large truck on a busy road after walking outside his house barefoot and in pajamas during a snowstorm. The 14-year-old jumped to his death from the balcony of a ninth-floor flat. Later, a teenage girl was narrowly prevented from jumping to her death from a window within days of starting a course of the flu drug. By November 2005, it had been reported that 12 Japanese children had died while on the drug and that others had experienced hallucinations, encephalitis and other symptoms.

Despite these alarming reports, the FDA voted not to issue a warning about the drug's potential for causing abnormal behavior. Instead, the FDA chose to warn of Tamiflu's potential for producing skin rashes. It wasn't until reports surfaced of more than 100 new cases of delirium, hallucinations and other abnormal psychiatric behavior in children treated with Tamiflu that the FDA changed course and added a warning label in November 2006.

Over the years, the FDA has been accused of causing high drug prices, keeping life-saving drugs off the market, allowing unsafe drugs on the market because of pressure from pharmaceutical companies and censoring health information about nutritional supplements and foods.

One such critic is Dr. David Graham, Associate Director for Science and Medicine and a senior drug safety researcher at the U.S. Food and Drug Administration. In his estimation, the FDA is ?responsible for 140,000 heart attacks and 60,000 dead Americans. That's as many people as were killed in the Vietnam War.? His words offer an insider's perspective on the fatal role he believes the FDA played in thousands of heart attacks and deaths caused by the pain medication Vioxx-a medication the FDA approved and initially failed to warn of its potential effects. Indeed, the Vioxx debacle was brought to America's attention when Congress was presented with evidence showing that among the estimated 20 million users of Vioxx, hundreds of thousands had died or suffered heart attacks as a result of taking the drug.
 
Other drugs approved by the FDA and later found to cause harm include dexfenfluramine, a diet drug whose post-marketing data indicated an increased risk of pulmonary hypertension, and troglitazone, a diabetes drug that carried with it the risk of liver failure and was later pulled from the market. Yet as Graham has pointed out, ?Rarely will they keep a drug from being marketed or pull a drug off the market.? The delays in taking action on problematic drugs was addressed by Dr. Sidney Wolfe, director of the Public Citizen's Health Research Group, in a statement before the Institute of Medicine Committee in January 2006: ?In too many instances, serious post-marketing safety problems identified by the Office of Drug Safety have not been acted upon because of resistance from FDA management and from the review division that originally approved the drug.?

But the pharmaceutical companies also bear the responsibility-and the blame-for unsafe drugs being approved and put out on the market. "The FDA assumes the drug is safe and now it's up to the company to prove that the drug isn't safe," remarked Graham. "Well, that's a no- brainer. What company on earth is going to try to prove that the drug isn't safe?"

It should come as no surprise that the pharmaceutical companies have the federal government in their hip pocket. According to a 2005 report from the Center for Public Integrity, "The pharmaceutical and health products industry has spent more than $800 million in federal lobbying and campaign donations at the federal and state levels in the past seven years." In fact, no other industry has spent more money to sway public policy during that period. The report continues, "The drug industry's huge investments in Washington-though meager compared to the profits they make-have paid off handsomely, resulting in a series of favorable laws on Capitol Hill and tens of billions of dollars in additional profits."

With an estimated 200,000-plus people dying every year from prescription drugs, Graham believes "Americans and Congress should be screaming bloody murder. They should be beating on the doors of the FDA demanding change."
 


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THOUGHT FOR THE DAY!
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" What determines your health is what you do seven days a week, not what you do at the one Christmas party."
 


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 TODAY'S HEALTH TIP

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Prostate Cancer Risks Assessed

The Department of Community Medicine and General Practice at the Norwegian University of Science and Technology studied the risk factors and found two unlikely candidates, according to the British Journal of Cancer.

Divorced men have a higher risk of prostate cancer than married men, and the risk of prostate cancer is greater among men with higher socio-economic status, larger incomes and more education.

 


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 HEALTH TODAY
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Study Links Heartburn Drugs, Broken Hip
Dec 26, 2006
By CARLA K. JOHNSON

CHICAGO (AP) - Taking such popular heartburn drugs as Nexium, Prevacid or Prilosec for a year or more can raise the risk of a broken hip markedly in people over 50, a large study in Britain found.

The study raises questions about the safety of some of the most widely used and heavily promoted prescription drugs on the market, taken by millions of people.

The researchers speculated that when the drugs reduce acid in the stomach, they also make it more difficult for the body to absorb bone-building calcium. That can lead to weaker bones and fractures.

Hip fractures in the elderly often lead to life-threatening complications. As a result, doctors should make sure patients have good reason to stay on heartburn drugs long term, said study co-author Dr. Yu-Xiao Yang of the University of Pennsylvania School of Medicine.

"The general perception is they are relatively harmless," Yang said. "They often are used without a clear or justified indication for the treatment."

Some people find relief from heartburn with over-the-counter antacids such as Tums, Rolaids and Maalox. But for others, those medicines do not work well. Moreover, heartburn can be more than a source of discomfort. People with chronic heartburn can develop painful ulcers in the esophagus, and in rare cases, some can end up with damage that can lead to esophageal cancer.

Dr. Sandra Dial of McGill University in Montreal, who was not involved in the study but has done similar research, said patients should discuss the risks and benefits with their doctors and taper off their use of these medicines if they can.

Nexium, Prevacid and Prilosec are members of a class of drugs known as proton pump inhibitors. The study found a similar but smaller risk of hip fractures for another class of acid-fighting drugs called H2 blockers. Those drugs include Tagamet and Pepcid.

The study, published in Wednesday's Journal of the American Medical Association, looked at medical records of more than 145,000 patients in England, where a large electronic database of records is available for research. The average age of the patients was 77.

The patients who used proton pump inhibitors for more than a year had a 44 percent higher risk of hip fracture than nonusers. The longer the patients took the drugs, the higher their risk.

The biggest risk was seen in people who took high doses of the drugs for more than a year. That group had a 2 1/2 times greater risk of hip fractures than nonusers.

Yang said that for every 1,262 elderly patients treated with the drugs for more than a year, there would be one additional hip fracture a year attributable to the drugs. For every 336 elderly patients treated for more than a year with high doses, there would be one extra hip fracture a year attributable to the drugs.

Dr. Doug Levine of AstraZeneca PLC (AZN), which makes Nexium and Prilosec, said the study does not prove that proton pump inhibitors cause hip fractures. It merely suggests a potential association, he said. Doctors need to monitor their patients for proper dosage and watch how long they take the drugs, Levine said.

Julia Ellwanger, a spokeswoman for TAP Pharmaceutical Products Inc., which markets Prevacid, said proton pump inhibitors' safety has been well-established by rigorous studies, and the new study does not prove or disprove a connection to hip fractures.

Dr. Alan Buchman of Northwestern University, who was not involved in the research, said the study should not change medical practice, since doctors already should be monitoring the bone density of elderly people taking the drugs and recommending calcium-rich diets to all patients.

"Most people are not taking enough calcium to start with," he said. He also wondered if a similar result would have been found in a sunny climate, because vitamin D from sunshine helps with calcium absorption.

Also, Buchman said it not known whether the acid-fighting drugs prevent esophageal cancer. He said the risk of esophageal cancer has been exaggerated in the marketing of these drugs.

"I think the risk has been overplayed and scared the community," Buchman said.

Heartburn medicines are heavily are advertised in "Ask your doctor about ..." commercials in this country, particularly during the evening news.

Nexium is the third biggest selling drug in the world, behind the cholesterol medicine Lipitor and blood thinner Plavix, with global sales totaling $5.7 billion last year, according to IMS Health, which tracks drug sales.

Yang and his co-authors disclosed in the paper that they have worked as consultants and received speaking fees from companies making acid-fighting drugs. The study was funded by the National Institutes of Health and the American Gastroenterological Association/GlaxoSmithKline Glaxo Institute for Digestive Health.

Men in the study had a higher drug-associated risk of hip fracture than women, possibly because women may be more aware of osteoporosis and may get more calcium in their diets, Yang said. He plans more research on whether calcium-rich diets or calcium supplements can prevent the problem.

JAMA 


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    ENVIRONMENTAL REPORT      
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Living Near Busy Street Ups Breathing Problems
December 28, 2006
 

NEW YORK - The closer people live to a main road, the more likely they are to suffer from respiratory symptoms such as breathlessness and wheezing, a new study from Switzerland shows.
 
"These findings from a general population provide strong confirmation that living near busy streets leads to adverse respiratory health effects," Dr. Lucy Bayer-Oglesby, of the University of Basel, and colleagues write in the American Journal of Epidemiology.
While outdoor air pollution -- especially tiny particles that can be breathed deep into the lungs--is known to be hazardous to people's health, to date no researchers have looked at how proximity to main roads affects respiratory symptoms in a general population, Bayer-Oglesby and her team note.

To investigate, they looked at data from a two-part study of air pollution and lung disease. It involved 9,651 randomly selected men and women aged 18 to 60 who enrolled in the study in 1991, 8,047 of whom re-enrolled for the second phase of the study in 2002.

People's risk of having attacks of breathlessness increased by 13% for every 500-meter segments of main street located within 200 meters of their home. The risk of such attacks among people who had never smoked fell by 12% for each additional 100 meters between their homes and a main street.

Individuals whose homes were within 20 meters of a busy road were 15% more likely to regularly have phlegm in their breathing passages, while they were 34% more likely to have wheezing with breathing problems.

The effects of traffic on respiratory health were stronger for men and for people who had never smoked.

The effects of living near main streets were weaker in 2002 than in 1991, which may have been due to stricter requirements on auto emissions, the researchers note.

"Living close to main streets or in a dense street network increases the risks for certain respiratory symptoms in adults, particularly for asthma-related symptoms such as attacks of breathlessness and wheezing and for bronchitic symptoms such as regular cough and phlegm," they conclude.

SOURCE: American Journal of Epidemiology, December 15, 2006.

 


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