This medicine began to be used in the treatment of diabetes in the year 2000 as a medicine is controlling the blood sugar for people with diabetes type II, but also made it clear on several occasions, there is a problem a very important increase the incidence of heart attack for its users, and appeared this problem in mid-2007, after publication Research Dr.Nissen in the medical journal New England Journal AFP Medicine (NEJM) has I had the opinion of users Avandia in the meantime, but that view has changed now because of the developments that have taken place on the decisions and recommendations of international organizations specialized in diabetes and in particular the Organization medicine and food Administration (FDA) and the European Medicines Agency (EMA) So what happened?
In fact, I've had the U.S. Food and Drug Administration (FDA) in July 2010 restricting Alavaye! The organization then U.S. Food and Drug Administration (FDA) since several weeks ago to prevent Officials study Tide (TIDE) continuation give Avandia or in other words stopped. Has also applied for re evaluation of RECORD study. What does it mean to restrict medicine Alavaye? Where it recommended the following:
1 - has allowed for Avandia eaters continue to be taken, but they have to refer to your physician to review on a case by case basis after the new developments and asked the doctors to clarify the risks of the medication.
2 - not the doctor give Avandia to infected do not use this medication only after the failure of a doctor to control blood sugar and after that have the doctor using all other drugs used to control blood sugar and that there be an obstacle to the use of placebo, a drug from the same family, but no risk such as those of Avandia and this drug is Pioglitazone) known Actos and then after that the patient must agree on use Avandia after the doctor to clarify the problems associated with medicine Avandia.
In fact it is hard to be there diabetic these conditions to give medication Avandia., And Of surprise that the Organization of medicine and food Administration (FDA) did not you pull the drug from the market (but probably will do so soon), but I believe that the Organization of medicine and food Administration (FDA ) waiting for from the British manufacturer Jlazcomit Kline (GSK) that you are (any company) to stop manufacturing the drug can now be the same .. We'll see?
However, the European Medicines Agency (EMA) was more pronounced with medication Avandia, has the European Medicines Agency (EMA) on 23/9/2010 (yesterday) to suspend medicine Alavaye. But what is the meaning of comments medicine? Comment medicine differs from the withdrawal of the drug from the market, The suspension medicine is to prevent the description of this medicine to patients without diabetes (new) and replace it if the patient with diabetes used, and prevents the doctors working in Europe from the use of this drug until further notice any that this drug will disappear in a few months from now.I have asked the European Medicines Agency (EMA) from glascosmith manufacturer Klein (GSK) to carry out other scientific or bring other information to Athbat that the benefits of the drug Alavaye more than harms then will the European Medicines Agency (EMA) to lift the suspension on the drug. And re-described for European patients.
But if it succeeds glascosmith Kline (GSK), to bring these has succeeded in making "The camel goes into the needle."
So after this, what being done with diabetes, which is used in medicine Avandia?
He should consult his doctor and ask him to replace him with another medication.
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