Topiramate | MIGRELIEF

Posts Tagged ‘Topiramate’

Migraine Prevention Drugs, Topiramate and Amitriptyline Prove No Better than Placebo in Children

November 12th, 2016

Alternative for Children's Migraines

Scientist and patent holder, Curt Hendrix explain the science behind the success of MigreLief migraine formulas.

Last month, Akeso Health Sciences attended annual conferences of the AAP (American Association of Pediatricians) and the CNS (Child Neurology Society) to exhibit its migraine supplements as effective nutritional support for children aged 2+ suffering either chronic or episodic migraine.

It was great to meet face-to-face with some of the neurologists, headache specialists and other healthcare professionals who have been recommending MigreLief supplements for years. Both MigreLief formulas, “daily maintenance” and “as-needed help” were well received.
It was at the recent CNS convention that we were first informed of the study regarding the use of topiramate and amitriptyline for migraine prevention in children. The study was published simultaneously with its presentation at the annual meeting of the Child Neurology Society in Vancouver.

A randomized, double-blind, placebo-controlled trial of 328 children and adolescents aged 8-17 who were diagnosed with migraines (with our without aura) concluded that amitriptyline and topiramate proved no better than placebo at preventing migraine in children and were associated with adverse side-effects.

In the study, the participants recorded the number of headaches they experienced during a 28 day baseline period and then were given either a placebo, topiramate, or amitriptyline during a 24 week trial period. The drug doses were increased every 2 weeks over an 8 week period with doses modified according to side-effects. In the end, no differences in effectiveness were seen between the two drug groups and the placebo group, however, the authors observed higher rates of adverse side-effects overall in the active treatment groups than the placebo.

Amitriptyline users more often reported fatigue (30%) and dry mouth (25%), whereas topiramate users more often reported parathesia (31%) (burning or prickling sensation that is usually felt in the hands, arms, legs, or feet, but can also occur in other parts of the body), and weight loss (8%).  Other side-effects reported with topirimate included, fatigue (25%), dry mouth (18%), memory impairment (17%), aphasia (16%), cognitive disorder (16%), and upper respiratory tract infection (12%).  Serious adverse events included altered mood in three patients in the amitriptyine group and one suicide attempt in the topiramate group.

Before the trial was concluded, the Food and Drug Administration approved topiramate for the treatment of episodic migraine in adolescents aged 12-17 years.

“Given the null outcome in this trial and the adverse events and serious adverse events reported in the amitriptyline and topiramate groups, the data do not show a favorable risk-benefit profile for the use of these therapies in pediatric migraine prevention, at least over the 24-week duration of the trial,” the study authors concluded.

If you are a parent of a young migraine sufferer, consider MigreLief nutritional migraine supplements.

To the Best of Health,

Curt Hendrix, M.S., C.C.N., C.N.S.
Chief Scientific Officer
Akeso Health Sciences

 

Click to view original article published online Oct 27, 2016 – The New England Journal of Medicine.

Click to view Children’s MigreLief product information pdf – Children’s MigreLief and Fast-Acting MigreLief NOW (Age 2+)

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MIGRAINE DRUG LINKED TO RISK OF WEAKENING WOMEN’S BONES

May 13th, 2011

A WELL KNOWN DRUG USED TO PREVENT MIGRAINES MAY DO SO AT THE RISK OF WEAKENING WOMEN’S BONES.

In an article published in the medical journal “Headache” and written by the departments of neurology, pediatrics, obstetrics and gynecology of the University of Toledo College of Medicine, the researchers stated that the anti-epileptic drug, Topiramate (Topamax) reduced bone mineral density in women who used the drug to treat their migraines.

It was found that 53% of women, who had used topiramate, were found to have osteopenia, which is bone loss that is not normal but not yet diagnosable as osteoporosis.

The researchers also found a correlation between the degree of bone loss and the amount of time the women were using the topiramate.

While prevention of migraine is definitely the preferable way to go for chronic migraine sufferers, other safe and natural choices are available that do not introduce bone loss or other side-effects associated with this drug.  For more information please go to www.migrelief.com

FDA WARNING: TOPAMAX SIGNIFICANTLY INCREASES THE RISK OF BIRTH DEFECTS IN PREGNANT USERS

March 20th, 2011

FDA Warning-Topiramate High Risk Birth DefectsTopiramate (brand name Topamax) an anti-seizure prescription drug that is also used for migraine prevention, has been found to significantly increase the risk of birth defects when used by pregnant women.

Infants who were exposed to Topamax while in the womb had a 1.4% prevalence of oral clefts (cleft palates) compared to just .38-.55% with other antiepileptic drugs.

Dr. Russell Katz of the FDA states“Before topirmate is prescribed, health care professionals should warn patients of childbearing age about the potential hazard to the fetus if a woman becomes pregnant while taking this drug.”  “Alternative medications that have a lower risk of birth defect should be considered.”

For those women of child-bearing age, who are also suffering with chronic migraine headaches, and don’t want to expose themselves to this risk,  MigreLief   the well-known, safe and very effective nutritional medicine for migraine relief, is a great alternative.

More Common and Serious Side Effects of Topamax