Posts Tagged ‘dizziness’

USA Today: Researchers say nearly 1 million kids diagnosed “ADHD” simply because they’re youngest in their class

Tuesday, August 17th, 2010

USA Today
By Liz Szabo
August 17, 2010

Nearly 1 million children may have been misdiagnosed with attention deficit hyperactivity disorder, or ADHD, not because they have real behavior problems, but because they’re the youngest kids in their kindergarten class, researchers say.

Kids who are the youngest in their grades are 60% more likely to be diagnosed with ADHD than the oldest children, according to a study out today from Michigan State University, given exclusively to USA TODAY. A second study, by researchers at North Carolina State University and elsewhere, came to similar conclusions. Both are scheduled for publication in the Journal of Health Economics.

TEENS: 1/3 with ADHD drop out or delay graduation

About 4.5 million children have been diagnosed with ADHD, according to the studies.

Misdiagnosing children can have long-lasting effects, says assistant professor of economics Todd Elder, author of the Michigan State study. In fifth and eighth grade, the youngest kids in a class were more than twice as likely to use Ritalin, a stimulant commonly prescribed for ADHD, compared with the oldest students, his study says.

While many parents say Ritalin has helped their kids, it also can have significant side effects, causing headaches, dizziness and even high blood pressure, according to the paper from North Carolina State.

The findings could influence the way that teachers evaluate children with ADHD symptoms — as well as complicate parents’ decisions about when to start children in kindergarten, Elder says.

Read entire article here:  http://www.usatoday.com/news/health/2010-08-17-1Aadhd17_ST_N.htm

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Pharmaceutical companies deceive public—case in point; Antidepressants

Thursday, July 29th, 2010

The Star Phoenix
By Mark Lemstra
July 29, 2010

We could save $2 billion a year on health-care costs in Saskatchewan while improving health outcomes if we adopt evidence-based protocols.

To do so, we need to find about $40 million of efficiency in each of about 50 areas.

This is the third article in a five-part series on depression. My first column discussed the limitations in diagnosing depression. The second presented literature reviews that concluded antidepressants are no more effective than placebos in treating depression.

This column explains how the drug companies deceive us. Let’s start with some general information and proceed to specific examples for antidepressants.

In 2008, the editor of the New England Journal of Medicine wrote an editorial for the Journal of the American Medical Association, titled: Industry sponsored research: A broken system?

Based on her tenure as the editor of the world’s most prestigious medical journal, Dr. Marcia Angell made some accusations. She wrote that drug companies often design studies, conduct the data analysis, decide which data will be included or suppressed, write the papers, pay for prestigious clinicians to put their name on papers already written by the drug company, and then decide how and when the paper will be published.

Dr. Angell concluded: “Drug companies now finance most clinical research on prescription drugs, and there is mounting evidence that they often skew the research they sponsor to make their drugs look better and safer. Physicians can no longer rely on the medical literature for valid and reliable information.”

She also published a best selling and award-winning novel, The Truth about Drug Companies: How They Deceive Us and What to Do About It.

Let’s look at some examples from anti-depressants.

A research team from the United States, which was skeptical about the benefits of antidepressants, used the Freedom of Information Act to obtain results from the U.S. Food and Drug Administration for all placebo-controlled trials. The team was startled to learn that 40 per cent of the studies had been suppressed because of negative results.

When all the studies were included, incorporating the negative studies, the authors concluded that “antidepressants are little more than active placebos, drugs with very little specific benefit, but with serious side-effects.”

The resulting publication in Prevention and Treatment made headlines around the world. And although regulatory agencies in Europe have begun to respond, there has been no response in North America.

At this point, let’s discuss the potential side-effects of antidepressants in a review from Harvard Medical School, titled: What are the real risks of antidepressants?

The most serious of these includes the increased risk of attempted suicide, especially among children. Other side-effects include insomnia, skin rashes, headaches, joint and muscle pain, stomach upset, nausea, diarrhea, reduced blood clotting capacity, stomach bleeding, uterine bleeding, tics, muscle spasms, trembling limbs, restlessness, severe anxiety, reduced sexual interest, reduced sexual performance, reduced sexual satisfaction, disturbed heart rhythms and reduced liver function.

There are also complications when antidepressants are taken with other drugs, and there is a long list of side-effects when antidepressant use is discontinued, including dizziness, loss of co-ordination, fatigue, burning sensations, blurred vision, insomnia, vivid dreams, nausea, diarrhea, flu-like symptoms, irritability, anxiety and crying spells.

Recently, the antidepressant Serzone was removed from the market after it was associated with hepatitis and liver failure.

The most worrisome side-effect is the increased risk of suicide attempt so let’s take a closer look.

Another review from the Food and Drug Administration found that not only do antidepressants provide no benefit to children, but the drugs are associated with a 50 per cent increase in suicidal behaviour.

Regrettably, these negative results, too, were buried by the drug companies.

Read the rest of this article here:  http://www.thestarphoenix.com/news/Pharmaceutical+companies+deceive+public/3336124/story.html

Previous articles in this series: Effect of antidepressants, placebos similar by Mark Lemstra
http://www.thestarphoenix.com/health/Effect+antidepressants+placebos+similar/3307896/story.html

Expanding mental disorders list adds to cost by Mark Lemstra
http://www.thestarphoenix.com/health/Expanding+mental+disorders+list+adds+cost/3280676/story.html

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Adderall, a drug commonly given to children diagnosed “ADHD”, associated with serious, life-threatening side effects

Monday, April 26th, 2010

EmaxHealth
By Deborah Mitchell
April 26, 2010

Adderall and Adderall XR, schedule II controlled substances composed of amphetamine and dextroamphetamine, have several Food and Drug Administration (FDA) approved uses. However, both prescribed and recreational use of these drugs, especially among young people, is associated with serious, life-threatening side effects.

The FDA requires that all amphetamines, including Adderall and Adderall XR (the long-acting version of Adderall), carry a black box warning, which means that medical research has demonstrated that these drugs carry a significant risk of serious, or even life-threatening, adverse effects. According to the Drug Enforcement Administration, both of these drugs have a “high potential for abuse” that “may lead to severe psychological or physical dependence.” In an attempt to stem such abuse, the federal government limits the amount of these amphetamine drugs that can be manufactured each year.

Adderall is a central nervous system stimulate approved by the FDA to treat attention deficit hyperactivity disorder (ADHD) and narcolepsy. Studies show that the side effects associated with Adderall XR include abdominal pain, anorexia (loss of appetite), asthenia (feeling of weakness), diarrhea, dizziness, dry mouth,elevated blood pressure, fever, headache, heartburn, infection, (including urinary tract infection), insomnia, nausea, tachycardia (rapid heartbeat), and weight loss.

The American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders notes that “Amphetamine, as with cocaine, can induce symptoms similar to those seen in obsessive disorder, panic disorder, and phobic disorders.” The Diagnostic and Statistical Manual notes that “high doses and long-term use of amphetamines are associated with erectile disorder and other sexual dysfunction. Use of Adderall can also induce schizophrenic-like states in children who are taking prescribed doses, according to The Journal of the American Board of Family Medicine.

Read entire article:  http://www.emaxhealth.com/1275/adderall-associated-serious-life-threatening-side-effects.html

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