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A free Ezine
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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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Monday March 10, 2008
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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
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work for you as well. Enjoy the week and do all that you can for your
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==================================
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
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2) 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!
4) 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
from Mega Bacterial Illnesses and growing as I write!!!"
Lena Sanchez a retired Medical Office Nurse &
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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?
~^~^~^~^~^~^~^~^~^~^~
TODAY'S HEALTH TIP
~^~^~^~^~^~^~^~^~^~^~^
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...
~^~^~^~^~^~^~^~^~^~^
HEALTH TODAY
~^~^~^~^~^~^~^~^~^~^~
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.
^~^~^~^~^~^~^~^~^~^~^~^~^~^~^
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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