Natural Health Education and Business Facts
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A Natural Environmental Health Facts Ezine
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A free Ezine aka newsletter  Here to Inform and Help You Become Healthier and Happier while Achieving Quality of life longevity! The sometimes controversial healthy alternatives versus traditional medicine also pro's and con's of both. Covering all health topics.
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928-636-9425
Monday  March 10, 2008
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This Ezine is available by subscription only and subscriber requests are kept on file!

I strive to bring you only the most timely, pro's & con's information for the betterment of your health without clogging the issue or your email box with a lot of  advertising and other such junk! If I am not 
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============================
=> IN THIS ISSUE!
============================


==> 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 and hopefully a health advocate for you and your family!

Seems rather strange preparing an ezine for Monday and not Ask Lena Health Q & A. This schedule will help me organize my life a bit more and hopefully will work for you as well. Enjoy the week and do all that you can for your healths sake!

Question or comment (good or not so good) Click Here 
Lena

Ezine archives  Click Here 
Ask Lena Health Q & A Archives  Click Here
Home Business Informative ezine Archives Click Here


Watch for Tuesday's "Ask Lena Health Q & A edition.
Get Your Health Question Answered Email Click Here Next week will publish on Wednesday's not Monday!
&
Tuesday's & Thursday's "Business Section of Ezine"
The newsletter/ezine for home based businesses and/or find the affiliate of your dreams!

To Read Past Issues Click Here


==================================
Something To Think About
============================

FDA Approves Nexium for Use in Children Ages 1-11 Years

The U.S. Food and Drug Administration approved Nexium (esomeprazole magnesium) for short-term use in children ages 1-11 years for the treatment of gastroesophageal reflux disease (GERD). The agency approved Nexium in two forms, a delayed-release capsule and liquid form. Nexium is approved in 10 milligrams (mg) or 20 mg daily for children 1-11 years old compared to 20 mg or 40 mg recommended for pediatric patients 12 to 17 years of age.

"This approval provides important information for appropriate dosing for children ages 1-11 years with GERD," said Julie Beitz, M.D., director of the FDA's Office of Drug Evaluation III in the Center for Drug Evaluation and Research. "Children prescribed this drug should be monitored by their physicians for any adverse drug reactions."

Nexium is part of a class of drugs known as proton pump inhibitors (PPIs). PPIs decrease the amount of acid produced in the stomach and help heal erosions in the lining of the esophagus known as erosive esophagitis.

FDA approved the use of Nexium in patients 1 to 11 years for short-term treatment of GERD based upon the extrapolation of data from previous study results in adults to the pediatric population, as well as safety and pharmacokinetic studies performed in pediatric patients. In one study, 109 patients 1-11 in age, diagnosed with GERD, were treated with Nexium once-a-day for up to eight weeks to evaluate its safety and tolerability. Most of these patients demonstrated healing of their esophageal erosions after eight weeks of treatment.

The most common adverse reactions in children treated with Nexium were headache, diarrhea, abdominal pain, nausea, gas, constipation, dry mouth and sleepiness. The safety and efficacy of Nexium has not been established in children less than one year of age.

Nexium is manufactured by AstraZeneca of Wilmington, DE.

www.fda.gov

LENA'S COMMENT: Given to children? Not smart!!! The safety in adolescence and adults hasn't proven safe either! Since Nexium shuts down the gastric valves that produce Hydrochloric acid, that is so very necessary in digestion, we can expect a huge onslaught of illnesses much earlier in life now due to the fact the body cannot digest the nutrients in the foods taken in making for quicker malnutrition and organs failing.


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SHOWCASE SPOTLIGHT 

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Ten (10) Reasons To Purchase and read
"ANTIBIOTIC ALTERNATIVES TO PREVENTING MEGA BACTERIA
 
1) To gain health knowledge"Knowledge is power!"  Without
it you leave yourself vulnerable and open to deception!
 
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Questions to ask your doctor to determine if antibiotics are necessary for the treatment of your problem!
 
3)
Know the five (5) diseases that do demand antibiotics!
 
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The Forgotten Antibiotic that will kill more than 640 bacteria and viruses!
 
5)
The most common antibiotic alternative natural
treatments and preventions!
 
6)
Natural Topical antiseptic easily mixed and stored!
 
7)
Listing of Healing Teas!
 
8)
Other Little known alternative natural remedies!
 
9)
Medical Terms explained!
 
10) How to take charge of your health!


If more changes aren't made soon the world is going to be one big Plague of Mega Illnesses Like Never Before, which has been  brought about by antibiotic usage out of control!


"Man has produced a monster with chemical antibiotics
that now cause the death of 8 people every minute
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Lena Sanchez a retired Medical Office Nurse & Health Consultant says," I
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=======================
THOUGHT FOR THE DAY!
=======================

A few of weeks ago, the FDA announced a permanent injunction against two food companies that were making claims such as: "Chemicals found in cherries may help fight diabetes."  Two different studies - one a lab study and one an animal study - have shown that anthocyanins (antioxidant compounds found in tart cherries) may help reduce the risk of type 2 diabetes. But the FDA has ordered the companies to stop making the claims "until the products are approved by the FDA as new drugs?"

That's right: as new drugs. Cherries what's next Lemons a drug?


 

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 TODAY'S HEALTH TIP

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Fever Confusion In Traditional Medicine!

How should you treat your child's fever? Maybe you shouldn't ask.

As reported in Pediatrics, researchers at Winthrop University Hospital in Mineola, N.Y., surveyed 161 physicians about how they treat fevers. Most doctors said they start treatment when a young patient's temperature reaches 101 degrees.

And half said they alternated between doses of acetaminophen (Tylenol) and ibuprofen (Advil or Nuprin).

When the doctors were asked why they switched between those two drugs, almost a third said they were following a recommendation by the American Academy of Pediatrics.

But according to the researchers, the American Academy of Pediatrics never issued any such advisory. In fact, the study's authors say, there have been no definitive studies on the best way to treat a fever -- in either children or adults.

LENA'S COMMENT: What I learned about fevers while working with 9 Pediatricians and hundreds of children weekly and a multitude of GP's, Internists and Surgeons! read Fever_and_Its_Necessity  to have an idea of how to treat a fever in your child or yourself...

 


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 HEALTH TODAY
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FDA Expands Warnings on Anemia Drugs
Mar 7, 2008
By MATTHEW PERRONE

WASHINGTON (AP) - Drug maker Amgen Inc. (AMGN) (AMGN) said Friday it expanded black box warnings about risks of death and tumor growth of its blockbuster anemia drugs.

The warnings approved by the Food and Drug Administration state that the company's drugs increased death and accelerated tumor growth in patients with early stage breast cancer and cervical cancer. Earlier labeling warned of similar risks in other types of cancer.

The changes apply to Thousand Oaks, Calif.-based Amgen's Aranesp and Epogen, as well as Johnson & Johnson' (JNJ) (JNJ)s Procrit. The drugs treat the blood-disorder anemia in patients with kidney failure and those on chemotherapy. Amgen manufacturers all three, though New Brunswick, N.J.-based J & J sells Procrit.

The language states that the problems occurred when doctors treated patients with elevated levels of the drugs, which increase red blood cell levels.
 
The action came less than a week before a meeting where government advisers are scheduled to review the risks of the blockbuster medications.

Since FDA began scrutinizing the drugs last March, shares of Amgen have sunk 27 percent. U.S. sales of its anemia treatments fell more than 10 percent to $6.3 billion for the year.

Wall Street analysts expect sales to fall further in 2008 following next week's review by FDA's cancer experts. The panel could recommend halting use of the drugs for certain types of cancers, or in all cancer patients. Recommendations will not apply to Amgen's Epogen, which is used almost exclusively by kidney failure patients on dialysis.

If FDA removes only some cancer indications, Amgen's anemia drug sales could lose between $150 million to $250 million for 2008, according to estimates by Goldman Sachs' analyst May-Kin Ho.

FDA twice updated anemia drug labels last year, most recently in November. Amgen disclosed new data in December on the drugs' risks in early stage breast cancer and cervical cancer patients, sending shares downward nearly 20 percent. The new label incorporates detail from those studies.

Bear Stearns analyst Mark Schoenebaum said the effect of Friday's changes would be minimal for Amgen, since cervical cancer accounts for about 1 percent of the Aranesp market. He also noted that the previous label already highlighted the breast cancer risks.

But Stanford Group Co. analyst Gregory Frykman said the new warnings could attract tougher regulations from Medicare, the government's health plan for seniors. Last summer Medicare ruled that it would only pay doctors to administer anemia drugs if they were prescribed at low levels.

Frykman said the new warnings could convince Medicare to scale back its policy again, perhaps only paying for the drugs when used in certain types of cancer.

Wall Street reacted positively to the news, sending shares up 1.02 cents, or 2.3 percent, to $45.20 in after-hours trading. Shares fell 14 cents to close at $44.18 in regular trading.

 

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    ENVIRONMENTAL REPORT      
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OUTSPOKEN SCIENTIST DISMISSED FROM PANEL ON CHEMICAL SAFETY

Deborah Rice, an award-winning toxicologist, was removed from a group of experts researching a widely-used flame retardant after industry lobbyists complained that she was biased.
By Marla Cone, Los Angeles Times Staff Writer

Under pressure from the chemical industry, the Environmental Protection Agency has dismissed an outspoken scientist who chaired a federal panel responsible for helping the agency determine the dangers of a flame retardant widely used in electronic equipment.

Toxicologist Deborah Rice was appointed chair of an EPA scientific panel reviewing the chemical a year ago. Federal records show she was removed from the panel in August after the American Chemistry Council, the lobbying group for chemical manufacturers, complained to a top-ranking EPA official that she was biased.

The chemical, a brominated compound known as deca, is used in high volumes worldwide, largely in the plastic housings of television sets.

Rice, an award-winning former EPA scientist who now works at the Maine Department of Health and Human Services, has studied low doses of deca and reported neurological effects in lab animals. Last February, around the time the EPA panel was convened, Rice testified before the Maine Legislature in support of a state ban on the compound because scientific evidence shows it is toxic and accumulating in the environment and people.

Chemical industry lobbyists say Rice's comments to the Legislature, as well as similar comments to the media, show that she is a biased advocate who has compromised the integrity of the EPA's review of the flame retardant.

The EPA is in the process of deciding how much daily exposure to deca is safe -- a controversial decision, expected next month, that could determine whether it can still be used in consumer products. The role of the expert panel was to review and comment on the scientific evidence.

EPA officials removed Rice because of what they called "the perception of a potential conflict of interest." Under the agency's handbook for advisory committees, scientific peer reviewers should not "have a conflict of interest" or "appear to lack impartiality."

EPA officials were not available for comment Thursday.

Environmentalists accuse the EPA of a "dangerous double standard," because under the Bush administration, many pro-industry experts have served on the agency's scientific panels.

The Environmental Working Group, a Washington, D.C.-based advocacy group, reviewed seven EPA panels created last year and found 17 panelists who were employed or funded by the chemical industry or had made public statements that the chemicals they were reviewing were safe. In one example, an Exxon Mobil Corp. employee served on an EPA expert panel responsible  for deciding whether ethylene oxide, a chemical manufactured by Exxon Mobil, is a carcinogen.

Sonya Lunder, a senior analyst at the Environmental Working Group, called it "deeply problematic from the public interest perspective" for the EPA to dismiss scientists who advocate protecting health while appointing those who promote industry views.

Lunder said it is unprecedented for the EPA to remove an expert for expressing concerns about the potential dangers of a chemical.

"It's a scary world if we create a precedent that says scientists involved in decision-making are perceived to be too biased," she said.

Rice was unavailable for comment Thursday.

In addition to her testimony for the Maine Legislature, Rice has been quoted in media reports saying there is enough scientific evidence to warrant bans on deca. "We don't need to wait another five years or even another two years and let it increase in the environment, while we nail down every possible question we have," she told the Seattle Post-Intelligencer last March.

In a May letter to an assistant administrator at the EPA, Sharon Kneiss, a vice president of the American Chemistry Council, called Rice "a fervent advocate of banning" deca and said she "has no place in an independent, objective peer review." She told the EPA that Rice's role on the panel "calls into question the overall integrity" of the EPA's evaluation of chemicals and that Rice may have influenced the other panelists in their review of deca.

Top EPA officials met with the industry group's representatives in June and promised to take action, according to a letter that EPA Asst. Administrator George Gray sent to the group last month. In that letter, Gray said the EPA found "no evidence" that Rice "significantly influenced the other panelists."

Environmentalists are concerned that Rice's removal could result in a less protective standard.

After EPA officials dismissed her from the five-member panel, they removed her comments from the panel's report on deca and removed all mention of her. Three months later, at the request of the chemical industry group, the EPA added a note to the panel report that Rice was removed "due to a perception of a potential conflict of interest" and that none of her comments were considered in their review of the chemical.

EPA documents show that Rice's comments while serving on the panel focused on technical, scientific issues. For example, she advised the EPA to consider the cumulative effects of not just deca,  but chemicals with similar neurological effects.

Rep. Henry Waxman (D-Los Angeles), chairman of the Committee on Oversight and Government Reform, said he was disturbed by Rice's dismissal and the Environmental Working Group's findings about pro-industry panelists.

"If this information is accurate, it raises serious questions about EPA's approach to preventing conflicts of interest on its expert scientific panels," Waxman said.

The conflict of interest policies of another environmental institute, the National Toxicology Program, also has come under fire. Last March, a major consultant for a federal center that evaluates reproductive hazards of chemicals was fired after The Los Angeles Times reported that the firm had financial ties to 50 chemical companies or associations.

Rice specializes in neurotoxins -- chemicals that harm developing brains. Before she went to work for the state of Maine, she was a senior toxicologist at the EPA's National Center for Environmental Research, where she had a major role in setting the EPA's controversial guideline for exposure to mercury in fish.

In 2004, the EPA gave Rice and four colleagues an award for what it called "exceptionally high-quality research" for a study that linked lead exposure to premature puberty in girls.

Many toxicologists and other environmental scientists have said they are highly concerned about flame retardants known as PBDEs, polybrominated diphenyl ethers.

In laboratory tests, PBDEs have been found to skew brain development and alter thyroid hormones, slowing the learning and motor skills of newborn animals.

Two of the compounds, called penta and octa, were banned in 2004. Before the ban, amounts in human breast milk and wildlife were doubling in North America every four to six years, a pace unmatched for any contaminant in at least 50 years. Now they are decreasing.

Scientists had initially thought that the deca compound was not accumulating in people and animals as the other PBDEs were. But it appears that deca turns into other brominated substances when exposed to sunlight, and now many scientists say it, too, is building up in the environment worldwide. Deca has similar effects on animals' developing brains as the banned PBDEs.

The chemical industry contends that low doses pose no danger and that the compound is necessary to prevent fires in many consumer products. In addition to TVs and other electronics, deca is used in furniture textiles, building materials and automobiles. About 56,000 tons were used worldwide in 2001, mostly in the United States and Asia.

Only Maine and Washington state restrict use of deca; both passed laws last year that phase out some uses. Similar bills have been introduced  in California but have not passed.

marla.cone@latimes.com

 


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