Showing posts with label Treatment. Show all posts
Showing posts with label Treatment. Show all posts

Wednesday, December 8, 2010

ADHD Treatment Without Medication


Drug companies say ADHD medication subdues symptoms - however, many parents say it's not symptoms medication controls, it's the children. Medication may stop some symptoms and ADHD crime, but children can end up like walking zombies. In worst cases, children are so subdued they die. Maybe it's time parents used an ADHD treatment without medication? There are many kinder therapies to choose from.

An Internet search for "Ritalin death" shows over a million pages. Are there better ways to help children's ADHD directly, without such terrible risks? Actually, yes, there are...

The title of this article says it all. "ADHD Treatment Without Medication". Another ADHD definition Internet search, "ADHD treatment without medication" shows 2/3rds of a million pages - almost as many pages as there are for "Ritalin deaths". So parents can choose ADHD drugless therapy options, without risk of serious side effects or death. University researched therapies are most likely to help safely.

To choose the safest and best ADHD therapy option, for treating ADD without medication, parents can search online. Changing just one word in a search can make a big difference. For example:


parents could search online for a good "university" because that shows the therapy has credibility with the establishment, (examples below are for the "University of London");
always include the word "research" or "researched" because that means the therapy has been tested and proven;
use "therapy" (although the word "treatment" might help);
add "drugless" or "drugfree".
Any combination of the above may help you search ADHD direct, and find a good quality therapy to help ADHD or ADD symptoms in children. Here are two examples - copy and paste these search terms into your search bar...

1.University of London research drugless ADHD treatment

2. University of London research ADHD therapy

Any good university is worth exploring for a researched therapy. If you're unsure which university to research, change the ADHD definition by leaving out university and used the word "researched". For example:

3. Drug-free researched adhd therapy

4. Researched ADHD therapy

Searches like these reveal good quality therapies that are drugfree and safe.

You could also search for specific doctors recommendations.

For example search for "Doctor Rita Chavez ADHD". Describing one therapy, she said:

"As head of a busy hospital clinic, I want patients to enjoy the quickest and cheapest cure. Yet drugs like Ritalin and Concerta can have severe side effects.

"As a medical doctor I need patients to be safe.

"Having seen these results I recommend doctors and psychologists to refer patients from any country as an early intervention."

Search on the internet for other doctor comments. A recommendation similar to Dr Chavez should reassure parents they're making the right decision.

So treating ADD without medication is possible. And this may reduce ADD symptoms in children, improve ADHD behaviour and prevent ADHD crime.

Good luck in your search.

Although if you search well, you won't need luck - you'll just lead a happier drugfree family life.

Finally...

Free ADHD diagnosis for ADD or ADHD is now available

All families needing an ADHD definition and whose child may need a test for ADD ADHD can get FREE ADD ADHD testing of the child's symptoms. The free online testing for ADHD and ADD symptoms in children is globally recognised as valid. Parents may then help ADHD direct.

If the ADD / ADHD assessment shows symptoms are present, find how to help a child's ADD or ADHD, maybe forever - including treating ADD without medication!








Learn more about ADHD treatment without medication with Tri Plan therapy. 'ADHD Tri Plan' gives free online tests and and 96.9% experience relief of symptoms of ADD and ADHD from any cause. Also helps schoolwork! Parents easily learn safe therapy via online videos. Save time - and money!

ADHD Tri Plan therapy received ethics approval and has been researched via the University of London, and achieves a remarkable success rate - 90.9% of children are at least partially helped within 3 weeks. Assessments of children one year after therapy showed 96.9% were helped.

Contact Pam Bryan via the contact page at http://www.adhd-triplan.com

For interviews and direct queries, phone:
United States: +1 786-245-7815
United States: +1 917-675-3395 (New York)
United Kingdom: +44 (0)20 8133 0422 (London)
Australia: +61 (0)2-8005-8442 (Sydney)

Copyright (c) 2009 "ADHD Tri Plan" - All Rights Reserved Worldwide.


Tuesday, December 7, 2010

Tailor Made Treatment for ADHD


Tailor made treatment for ADHD is in its infancy but the medical research community is moving faster than ever and our understanding of the complex neurotransmitter issues at work in ADHD is growing. This understanding is enabling us to better medically target individual brain differences when treating ADHD. The need for tailored treatment for ADHD stems from the puzzling fact that while one drug may work beautifully for one ADHD patient, it can be a treatment disaster for another. Some of these differences in treatment response may be related to subtype differences while others are related to individual differences.

There may be medical reasons, related to individual physiology, that explains why one Inattentive ADHD (ADHD-PI) patient will respond to coffee and another patient will have a bad reaction to coffee. Why a stimulant will work great for one kid with Hyperactive Impulsive ADHD (ADHD-HI) and horribly for another child with combined type ADHD (ADHD-C). Recent research, for instance, has allowed us to learn that some people have a genetic variant that causes them to metabolize caffeine very rapidly and abruptly while most of us metabolize caffeine slowly and continuously. Methylphenidate (Ritalin) and Amphetamine (Adderall) work in a unique way and research is pointing us towards an understanding of why some people with ADHD respond better to Ritalin and others respond better to Adderall.

Atomoxetine (Strattera) and Guanfacine (Intuniv) work on the ADHD brain in a different manner than the stimulant treatment for ADHD and some people benefit from these drugs while others have no effect from them or adverse effects from them. A new class of drug called a Histamine 3 (H3) receptor antagonist is in development and has shown promise in the treatment of ADHD. The H3 receptor antagonist work by enhancing the release of neurotransmitters. This new drug may help people that have had failed treatment responses to other drug therapies. The neurotransmitter receptors agonist and antagonist in our brains and bodies work differently in each of us and biological markers for this neurotransmitter activity are becoming more readily available. Physicians will soon have tools that will take some of the guesswork out of how you will respond to certain medical interventions.

These lab test and biological markers are, at the moment, prohibitively expensive and not readily available but the ready availability and affordability of this testing is not as far off as it was even a year ago. Genetic testing will also become more affordable and available which is important because genetics also plays a role in our response to treatment.

As researchers add medication to the ADHD arsenal, we will find that some patients will be uniquely helped by new medications like the H3 receptor antagonist and the Alpha-2 Adrenergic receptor agonist such as Intuniv while others will not be. We will see individual variations in the response to these medications and these variations may not always be related to the subtypes of ADHD. It is possible that Intuniv will help certain people with Inattentive ADHD (ADHD-PI) while others will have no effect from this medication.

We are not yet at the stage of medical testing where we can perform one lab test and know how well someone may respond to a medication. Researchers are progressing in their understanding of the complex brain processes involved in ADHD and there are now, as a result, more medications available to treat ADHD and more tests that can be performed that allow physician to understand who may benefit most from an ADHD medication.

Recent discoveries into the unique physiological processes that cause ADHD and new treatment and testing options allow physicians to gain a better understanding of individual ADHD differences. The tailoring of ADHD treatment cannot be too far off.








For more information on Primarily Inattentive ADHD please visit Tess Messer at http://www.primarilyinattentiveadd.com/2010/02/why-blog.html. There you will find information on ADHD symptoms, ADHD treatment, alternatives to medications, Information on ADHD vitamins and supplements and much more. Looking forward to meeting you there!!


Thursday, December 2, 2010

ADHD Treatment - Safe and Effective Ways to Deal With the Symptom of ADHD


It concerns me greatly when I see the ADHD treatment that is being prescribed for many children today.

ADHD medicines may help with the symptoms, but the side effects often create a whole new set of problems to deal with.

ADHD, or Attention-Deficit Hyperactivity Disorder, is a neurobehavioral syndrome, which can be manifested as impulsivity, hyperactivity and inattention. People with ADHD tend to miss details and are usually averse to tasks that need decisiveness, organization or concentration, which is why ADHD treatment is recommended.

Pharmaceutical ADHD Medicines

Medicines for ADHD include non-amphetamine stimulants, amphetamine-based stimulants, non-stimulants, neuroleptic drugs, mood stabilizers, antihypertensive drugs and antidepressants. The most common ADHD medicines are not without side effects however.

Common side effects from this type of ADHD treatment include nervousness, abdominal pain, headaches, insomnia, cardiac arrhythmia, weight loss, vomiting, sinusitis, sore throat and dizziness. Other ADHD treatment medications might cause tics, a reduced stature, psychosis and moodiness.

Long term use of certain ADHD medicines has been linked to brain development abnormalities similar to those in cocaine users. Not all ADHD sufferers who use pharmaceutical treatments suffer from side effects but there is a high risk.

Behavioral Therapy and Psychotherapy

This type of ADHD treatment includes rewarding positive behavior, using the appropriate discipline for bad behavior and ignoring attention-seeking outbursts. This can work for children or adolescents suffering from ADHD but might not be the best solution for an adult with the syndrome.

For an adult with ADHD, psychotherapy might be recommended. This type of treatment can help an adult to identify how the illness has affected his or her work, education and relationships. The therapy sessions can also help an adult with ADHD to schedule projects and tasks, operate a self-reward program, record and remember important dates and improve time management skills.

Natural ADHD Medicines

If therapy does not seem to work and the side effects of medicines for this disease are too risky, what other ADHD treatment is there to try? Natural therapies include getting more sleep (many ADHD medications prevent this), improving nutritional intake through diet and supplements, homeopathy, and coaching.

Natural treatments for ADHD might contain ingredients such as gingko biloba which keeps the circulatory system healthy thus improving blood flow to the brain, skullcap which is a calming nerve tonic, chamomile which is soothing or gotu cola which supports and strengthens the brain and nervous system. There are many other natural ingredients that have been shown to extremely effective in dealing with the symptoms of ADHD.

Natural means of helping with ADHD have been found to work well on many individuals. They are also free of the debilitating side effects which are so common in pharmaceutical ADHD medicines. Some pharmaceutical ADHD pills and tablets have also been found to be addictive, which natural remedies are not.

In conclusion, the safest and best ADHD treatment is a combination of behavioral therapy and natural ADHD remedies. Be sure to get plenty of sleep, eat balanced and complete meals and drink lots of water. Everyone effected by attention deficit issues will notice great improvement with this type of ADHD treatment. Many people have found this to be the most effective approach, as well as the safest. Use the ADHD medicines as a last resort, not the first.








Terry Tobin has been a student of the link between nutrition and behavior for over 8 years. His research led him to finding natural ways of dealing with attention and mood issues in his own life and family. Terry is the editor of Help For ADHD where he shares what he has found to be effective, natural help for ADHD. If you or someone you know is dealing with ADD/ADHD and the behaviors associated with it, then visit Help For ADHD to learn more about effective ways to improve concentration and behavior.


Monday, November 29, 2010

Shionogi Announces FDA Approval Of KAPVAY™ - The First And Only Therapy Approved For Use With Stimulant Medication For The Treatment Of ADHD


Main Category: ADHD
Also Included In: Regulatory Affairs / Drug Approvals;??Pharma Industry / Biotech Industry
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Shionogi Inc., the U.S.-based group company of Shionogi & Co., Ltd., announced the U.S. Food and Drug Administration approval of the non-stimulant medication KAPVAY™ (clonidine hydrochloride) extended-release tablets, an extended-release oral formulation for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children and adolescents ages 6-17 years. KAPVAY™ is the only formulation of clonidine hydrochloride approved by the FDA for the treatment of ADHD, and is the first and only FDA-approved ADHD treatment indicated for use as add-on therapy to stimulant medication. KAPVAY™ can also be used as monotherapy when treating ADHD.

An oral, non-stimulant, twice-daily therapy, KAPVAY™ is a centrally acting alpha2-adrenergic receptor agonist. While the mechanism of action of alpha2 agonists in ADHD is not known, it is believed to involve the pre-frontal cortex (PFC) of the brain. Studies suggest that the PFC regulates attention and plays a critical role in impulse control, working memory and executive function.

"The FDA approval of KAPVAY™ represents an exciting milestone in the field of ADHD," said Donald C. Manning, MD, PhD, Chief Medical Officer of Shionogi Inc. "The extended-release formulation of KAPVAY™ minimizes the peaks and troughs in blood levels, thereby decreasing overactivation of the alpha receptors in the brain and periphery. We look forward to providing this important, beneficial treatment for ADHD to patients, both as monotherapy and add-on therapy to stimulants."

"ADHD is a complex disorder that requires individualized treatment. While there are prescription treatment options available, many ADHD patients on stimulants do not achieve adequate control of symptoms," explained Rakesh Jain, MD, MPH, Director of Psychiatric Drug Research for R/D Clinical Research at Lake Jackson, Texas, and an investigator in the clinical trials. "KAPVAY™, when added to a stimulant, addresses an unmet need, and improves ADHD symptoms beyond what is achieved by stimulants alone. This is a significant step forward for the treatment of ADHD to have an approved product for add-on therapy in our treatment armamentarium."

ADHD is a neurobehavioral disorder that occurs in childhood and may continue into adolescence and adulthood, which affects more than 4.5 million children ages 3-17 in the U.S. alone. Approximately 3-7 percent of U.S. school-aged children are believed to suffer from this disorder. Symptoms include difficulty staying focused and paying attention, difficulty controlling behavior, and hyperactivity/over-activity.

This approval is based on two Phase III studies, which demonstrated efficacy at 5-weeks that children and adolescents (6-17 years) with ADHD treated with KAPVAY™ experienced statistically significant improvements in core symptoms of ADHD inattention, hyperactivity and impulsivity. The most common and drug related adverse reactions (incident at least 5% and twice the rate of placebo) included somnolence, fatigue, upper respiratory tract infection (cough, rhinitis, sneezing), irritability throat pain (sore throat), insomnia, nightmares, emotional disorder, constipation, nasal congestion, increased body temperature, drug mouth and ear pain. Maintenance efficacy has not been systemically evaluated and patients who are continued on longer-term treatment require periodic reassessment.

About KAPVAY™

Administered orally, clonidine hydrochloride exerts its pharmacological effects as a centrally acting alpha2-adrenoceptor agonist. The formulation in KAPVAY™ is designed to delay the absorption of active drug in order to decrease peak to trough plasma concentration differences.

Important Safety Information

KAPVAY™ should not be used in patients with known hypersensitivity to clonidine.

KAPVAY™ has not been studied in children with ADHD less than 6-years old.

Use KAPVAY™ with caution in patients at risk for hypotension, bradycardia and heart block. Measure heart rate and blood pressure prior to initiation of therapy, following dose increases, and periodically while on therapy. Advise patients to avoid becoming dehydrated or overheated.

Somnolence and sedation have been observed with KAPVAY™. Consider the potential for additive sedative effects with CNS depressant drugs. Caution patients against operating heavy equipment or driving until they know how they respond to KAPVAY™.

Patients should be instructed not to discontinue KAPVAY™ therapy without consulting their physician due to the potential risk of withdrawal effects. KAPVAY™ should be discontinued slowly in decrements of no more than 0.1 mg every 3 to 7 days.

In patients who have developed localized contact sensitization or other allergic reaction to clonidine in a transdermal system, substitution of oral clonidine hydrochloride therapy may be associated with the development of a generalized skin rash, urticaria or angioedema.

Use in patients with vascular disease, cardiac conduction disease, or chronic renal failure: Monitor carefully and uptitrate slowly.

Clonidine may potentiate the CNS-depressive effects of alcohol, barbiturates or other sedating drugs.

Caution is warranted in patients receiving clonidine concomitantly with agents known to affect sinus node function or AV nodal conduction (e.g., digitalis, calcium channel blockers and beta-blockers) due to a potential for additive effects such as bradycardia and AV block.

Do not use KAPVAY™ concomitantly with other products containing clonidine.

About Alpha2 Agonists

The prefrontal cortex (PFC) which regulates attention appears to be an important area of the brain affected in patients with ADHD. Specifically, studies suggest that the PFC plays a critical role in impulse control, working memory and executive function. Postsynaptic alpha2-adrenoceptors are one of several biological receptors important for PFC function.

About ADHD

ADHD is a neurobehavioral disorder that most often occurs in childhood and may continue into adolescence and adulthood. There are three subtypes of ADHD: predominantly hyperactive-impulsive, predominately inattentive, and combined hyperactive-compulsive and inattentive, with the latter being the most common. ADHD symptoms fall under three main categories: inattention, hyperactivity and impulsivity, which can include behaviors such as trouble focusing, frequent daydreaming, excessive talking, fidgeting/squirming, chronic impatience and difficulty waiting their turn, depending on the category.

The cause of ADHD is not yet known. However, research has shown potential links to genetic and environmental factors. While there is no cure for ADHD, the disorder can be managed with a variety of treatments including parental education and training, behavioral therapy and prescription medication.

ADHD is one of the most common childhood psychiatric disorders. In the United States alone, more than 4.5 million children ages 3-17 have been diagnosed, as of 2006. Approximately 3-7 percent of U.S. school-aged children are believed to suffer from this disorder. Boys are also more than twice as likely to be diagnosed (11 percent) as girls (4 percent).

Forward Looking Statements

This announcement contains forward-looking statements. These statements are based on expectations in light of the information currently available, assumptions that are subject to risks and uncertainties which could cause actual results to differ materially from these statements. Risks and uncertainties include general domestic and international economic conditions such as general industry and market conditions, and changes of interest rate and currency exchange rate. These risks and uncertainties particularly apply with respect to product-related forward-looking statements. Product risks and uncertainties include, but are not limited to, completion and discontinuation of clinical trials; obtaining regulatory approvals; claims and concerns about product safety and efficacy; technological advances; adverse outcome of important litigation; domestic and foreign healthcare reforms and changes of laws and regulations. Also for existing products, there are manufacturing and marketing risks, which include, but are not limited to, inability to build production capacity to meet demand, unavailability of raw materials and entry of competitive products. The company disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise.

Source: Shionogi Inc

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Saturday, November 27, 2010

New Data Analyses On CONCERTA® Pediatric Treatment Include Insight On Handwriting Performance And Attention In ADHD


Main Category: ADHD
Also Included In: Pediatrics / Children's Health;??Clinical Trials / Drug Trials;??Pharma Industry / Biotech Industry
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Data presented at a major medical meeting include findings that demonstrate improved handwriting performance in children with Attention Deficit Hyperactivity Disorder (ADHD) when taking CONCERTA® (OROS® methylphenidate HCl Extended-Release Tablets CII) compared to placebo. This data, which was presented by McNeil Pediatrics™, Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc., is one of two sub-analyses presented today on pooled data from two randomized, double-blind, placebo-controlled studies examining CONCERTA® efficacy in patients in simulated classroom environments.

"Previous research suggests handwriting can be a challenge in children with ADHD, who may have impaired handwriting performance compared to children without ADHD,(1,2,3)" said H. Lynn Starr, M.D., director of Medical Affairs for Ortho-McNeil Janssen Scientific Affairs, L.L.C. "Based on this premise, we wanted to examine CONCERTA® treatment in this area more closely. We hope our efforts may provide insight for parents and healthcare professionals interested in this research."

In this sub-analysis (Poster 5.26), the effect of CONCERTA® on handwriting performance was evaluated in 139 patients with ADHD, ages 9 to 12, in simulated classroom settings that compared patients' handwriting skills when they were treated with CONCERTA® versus when they received placebo. Results showed patients had better handwriting performance on the days when they took CONCERTA® than on the days they took placebo.

Handwriting was assessed using the Test of Handwriting Skills-Revised (THS-R). The THS-R is a standardized assessment designed to evaluate neurosensory integration shown in print and cursive writing. In a review of previously published studies, children with ADHD scored significantly lower than children without ADHD using this measure.(1) In the CONCERTA® sub-analysis presented today, the mean THS-R standard scores showed patients scored 91.46 on the day they took CONCERTA® versus 87.03 on the day they took placebo (p<0.0001).

In a separate sub-analysis of data (Poster 5.27) from the pooled classroom studies, CONCERTA® was compared to placebo using a skill-adjusted math test that measures attention in ADHD, known as the PERMP (Permanent Product Measure of Performance).

In this analysis, all 139 patients ages 9 to 12 had a confirmed diagnosis of ADHD, and 15 patients also had a co-morbid math-based learning disability (LD). The PERMP provided patients a series of math problems during the laboratory school day. The patients' performance on problems attempted and problems correctly answered was used to evaluate the effect of CONCERTA® on attention and focus.

Results of this sub-analysis showed patients with a math LD had higher mean PERMP scores for both the number of math problems attempted (93.8 vs. 67.2, respectively; p<0.01) as well as the number of math problems answered correctly (87.8 vs. 63.0, respectively; p<0.01) following treatment with CONCERTA® compared to placebo. Similarly, patients with no math LD also had higher mean PERMP scores in both measures after treatment with CONCERTA® compared to placebo (114.2 vs. 81.6, respectively; p<0.0001; 109.9 vs. 76.8, respectively; p<0.0001).

Adverse events occurring in 10 percent or more of patients in either sub-analysis presented today were consistent with those previously reported for CONCERTA® and included decreased appetite, upper abdominal pain, headache, irritability and initial insomnia. Two patients discontinued due to adverse events. No serious adverse events or deaths were reported.

About the CONCERTA® Clinical Trials

The two posters presented today are secondary analyses taken from a data set comprised of two randomized, double-blind, placebo-controlled, crossover analog simulated-classroom trials examining the effects of CONCERTA® compared with placebo. The trials included a general population of children with ADHD and a wide range of endpoints based on standardized ADHD measurements, as well as observational input from subjects' parents, teachers and healthcare providers.

About ADHD

Attention Deficit Hyperactivity Disorder (ADHD) is a common and treatable medical condition characterized by inattention, hyperactivity and impulsivity that is estimated to affect about 5 million children(4) and 8 million adults(5) in the United States. While the exact cause of the condition is still unknown, scientists have focused their research on chemical messengers, or neurotransmitters, in the brain.(6) Studies suggest that 76 percent of ADHD is linked to family genetics,(6) so the condition may be more common among people who have a close relative with ADHD.(7)

About CONCERTA®

CONCERTA® is a prescription medication approved for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children, adolescents and adults ages 6 to 65, as part of a total treatment program that may include counseling or other therapies.

IMPORTANT SAFETY INFORMATION

Talk to your healthcare professional for a proper diagnosis and treatment of ADHD. Only a healthcare professional can decide whether medication is right for you or your child.

CONCERTA® should not be taken by patients who have: allergies to methylphenidate or other ingredients in CONCERTA®; significant anxiety, tension or agitation; glaucoma; tics, Tourette's syndrome or family history of Tourette's syndrome; current or past use of monoamine oxidase inhibitor (MAOI); esophagus, stomach or intestinal narrowing. Children under 6 years of age should not take CONCERTA®.

Abuse of methylphenidate may lead to dependence. Tell your healthcare professional if you or your child has had problems with alcohol or drugs; has had any heart problems, heart defects, high blood pressure or a family history of these problems; has had depression, abnormal thoughts or visions, bipolar disorder or seizure. Contact your healthcare professional immediately if you or your child: develops abnormal thinking or hallucinations, abnormal or extreme moods and/or excessive activity; or if aggressive behavior or hostility develops or worsens while taking CONCERTA®. Your child's healthcare professional should check height and weight often and may interrupt CONCERTA® treatment if your child is not growing or gaining weight as expected.

Stimulants may impair the ability of the patient to operate potentially hazardous machinery or vehicles. Caution should be used accordingly until you are reasonably certain that CONCERTA® does not adversely affect your ability to engage in such activities.

The most common adverse reaction (greater than 5 percent) reported in children and adolescents was upper abdominal pain. The most common adverse reactions (greater than 10 percent) reported in adults were dry mouth, nausea, decreased appetite, headache and insomnia.

References

(1) Racine MB, Majnemer A, Shevell M, et al. Handwriting performance in children with attention deficit hyperactivity disorder (ADHD). J Child Neurol. 2008; 23(4):399-406.

(2) Flapper BC, Houwen S, Schoemaker MM. Fine motor skills and effects of methylphenidate in children with attention-deficit-hyperactivity disorder and developmental coordination disorder. Dev Med Child Neurol. 2006;48(3):165-169.

(3) Raggio DJ. Visuomotor perception in children with attention deficit hyperactivity disorde combined type. Percept Mot Skills. 1999 Apr; 88(2):448-50.

(4) Centers for Disease Control and Prevention. ADHD: Data and Statistics.

(5) Adler, Lenard. Scattered Minds Hope and Help for Adults with Attention Deficit Hyperactivity Disorder. New York: Perigee Trade, 2007.

(6) Faraone, S.V., Perlis, R.H., Doyle, A.E., Smoller, J.W., Goralnick, J.J., Holmgren, M.A. and Sklar, P. (2005) Molecular genetics of attention-deficit/hyperactivity disorder. Biological Psychiatry, 57, 1313 - 1323.

(7) Faraone, S.V. and Biederman, J. Is ADHD Familial? Harvard Review of Psychiatry, January/February 2004.

Source: McNeil Pediatrics(TM)

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posted by Dr. Billy Levin on 31 Oct 2010 at 2:16 am

I was aware of the benefits on handwriting with Methylphenidae 34 years ago

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