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ADHD,ADD, Autism : FDA Agrees ADHD Drugs Cause Kids to Have Hallucinations
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From: Rene  (Original Message)Sent: 4/21/2006 11:40 PM
I personally find this umm a bit worrisome
 
 


FDA Agrees ADHD Drugs Cause Kids to Have Hallucinations
 
 
 An FDA committee has recommended that information about the risk of hallucinations in children be added to the labels of attention deficit hyperactivity disorder (ADHD) drugs.

They did not, however, argue in favor of a "black box" warning, the strongest type of warning that can be affixed to a medication, for either hallucinations or cardiovascular risks, out of concerns that doing so would scare patients away from the drugs.

This conflicts with an earlier panel's recommendation that the cardiovascular risks be given a black box warning. The FDA is likely to follow the more recent panel's advice.

The recent panel also did not recommend adding a suicide risk warning to the labels, although one such drug, Strattera, does already carry a black box warning about suicide risk.

They did recommend that the FDA create a medication guide explaining the possibilities of increased aggressive behavior, heart attack, stroke, and potential sudden death.

 
 USA Today March 23, 2006

Yahoo News March 23, 2006

 
 
 
 Dr. Mercola's Comment:

 
 Looks like there's going to be no black box warning for either the hallucinatory or cardiovascular risks of ADHD drugs despite evidence supporting this labelling. That's the bad news.

The good news is that it really doesn't matter as black box warnings aren't particularly effective. They tend to be a tactic drug companies and the FDA use to say they warned the doctors and the public before they finally pull the drug off the market.

This interim measure allows the drug company to earn significantly more profits. Unfortunately, many are harmed or killed because their physicians did not believe or heed the warnings.

Many of the drugs used to treat ADHD are not only potentially hazardous, but they are unnecessary if your child is treated appropriately. And, just because the FDA is leaning toward putting a warning on the label, however watered down, doesn't mean it will happen anytime soon either. Any updates on prescription labels may not appear for several years.

Interestingly, I just learned that the medical director of the physician's group at Northwestern Hospital in Chicago just put her son on krill oil and in 40 days noticed remarkable improvement. The results were so dramatic that she invited the major supplier of krill oil to come out to Chicago and speak to the physician group at Northwestern this week.

If you have a child with ADHD I would strongly recommend reviewing the interview we did with Dr. Lendon Smith shortly before he passed away.

If you or a loved one is suffering from ADHD, please remember there are plenty of safe, effective alternatives for treating this condition without the need for a toxic, hallucinogenic drug. Some particularly effective methods include:

Using plenty of animal-based omega-3 fats like  krill oil.

Spending more time in nature.

Balancing your intake of omega-3 and omega-6 fats.

Avoiding Processed foods, especially those containing artificial colors, flavors and preservatives.

Replacing soft drinks, fruit juices and pasteurized milk in yuor diet with pure water.

Reducing or  eliminating grains and sugars from your diet. 

From:   http://www.mercola.com/2006/apr/6/fda_agrees_adhd_drugs_cause_kids_to_have_hallucinations.htm

more hotlinks are in the body of the article including the ones to the 2 news articles.

 



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 Message 2 of 2 in Discussion 
From: ReneSent: 6/26/2006 4:43 PM
 


Strattera Gets Warning Label
The Food and Drug Administration warned doctors Thursday about reports of suicidal thinking in some children and adolescents who are taking Strattera, a drug used to treat attention deficit disorder. Manufacturer Eli Lilly & Co. announced that a black-box warning will be added to the drug's label in the United States. Such a warning is the most serious that can be added to a medication's label. In a statement, the FDA said it "is advising health care providers and caregivers that children and adolescents being treated with Strattera should be closely monitored for clinical worsening, as well as agitation, irritability, suicidal thinking or behaviors, and unusual changes in behavior, especially during the initial few months of therapy or when the dose is changed."

 

The Numbing Of American Kids
Young children are often prescribed psychotropic drugs for pain relief, anxiety, bed wetting and attention-deficit/ hyperactivity disorder. The number of preschoolers in the United States being prescribed antidepressants and stimulants soared 50 percent between 1991 and 1995s, despite limited knowledge about the effects of such drugs on young children. The number of 2 to 4 year-olds on psychiatric drugs including Ritalin and antidepressants like Prozac jumped 50 percent between 1991 and 1995, in a study of more than 200,000 preschool-age children. The number of children getting any of the drugs totaled about 100,000 in 1991, and jumped 50 percent to 150,000 in 1995. That year, 60 percent of the youngsters on drugs were age 4, 30 percent were 3 and 10 percent were 2-year-olds. In 2002, about 6 percent of all boys and girls were taking antidepressants, triple the rate in the period 1994-96. And about 14 percent of boys -- nearly one in seven -- were on stimulant drugs in 2002, double the number in 1994-96. Research in the United States found that Ritalin may cause lasting changes to the brain. In a study carried out by the Harvard Medical School, healthy rats given the drug in their infancy were found to have a reduced sense of pleasure and were more prone to signs of despair during adulthood. Are the children who take stimulant medications today setting themselves up for chronic adult depression? Perhaps.

 

Paxil and Other Antidepressants May Increase Risk of Suicide In Children
Mosholder, a child psychiatrist, reviewed data from 20 clinical trials involving more than 4,100 children and eight different antidepressants. His preliminary analysis, according to two FDA sources familiar with the report's contents, concluded that there was an increased risk of suicidal behavior among children being treated for depression with Paxil and several other antidepressants. The use of antidepressants and other psychiatric medication among children has more than tripled in recent years and now approaches adult usage rates, according to a January 2003 study in the Archives of Pediatric and Adolescent Medicine. Study author Julie Zito, an associate professor of pharmacy and medicine at the University of Maryland, estimates that more than 1 million American children used antidepressants in 2000.

Just Say No Campaign Seems Ironic
I find it ironic that while our children are lining up to attend a “Just Say No To Drugs Talk,�?their being dispensed their daily Ritalin, Strattera, or other mood altering drug. Implying that there is a drug for every symptom only increases the false belief that we can self medicate away our fears and inadequacies with illegal mind altering substances.

Paxil And Birth Defects
The Food and Drug Administration is warning that a study has suggested that the antidepressant Paxil may be associated with birth defects. Paxil's manufacturer, GlaxoSmithKline, said it will include the results of the study in the drug's list of precautions. A retrospective study found increased numbers of babies born with birth defects to women who were taking Paxil during the first trimester of pregnancy, as compared with women on other antidepressants, according to the FDA and the company. To learn more about anxiety and depression please click on the link below to view a past newsletter.

 Health News from Dr. Murphree