Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Friday, May 20, 2011

Europe approves Pfizer blood thinner

http://www.wane.com/dpps/health/healthy_living/europe-approves-pfizer-blood-thinner_3817521
I'm wondering if this does not require the INR blood test.

Will be available in all EU countries

Updated: Friday, 20 May 2011, 3:54 PM EDT
Published : Friday, 20 May 2011, 3:54 PM EDT
NEW YORK (AP) - Drugmaker Pfizer said Friday that European regulators have approved its highly-anticipated blood thinner Eliquis to prevent blood clots in patients who have had hip or knee replacement surgery.
The approval by the European commission means the drug, known as apixaban, will be available in the 27 countries of the European Union. Pfizer Inc. co-developed the drug with Bristol-Myers Squibb, which will share the profits.
The drug was approved based on two studies that showed better outcomes for patients taking twice-daily Eliquis rather than receiving an injection of the typical current treatment. Bleeding side effects were approximately the same between the two groups. All patients studied had undergone orthopedic surgery to replace a knee or hip, a procedure that raises the risk of blood clots.
Eliquis has been touted as a potential blockbuster drug for its ability to prevent blood clots without the bleeding side effects of older drugs like warfarin. However, last year the companies had to halt a 10,000-patient study of the drug in people with a history of heart disease after an unexpected number of bleeding side effects.
Apixaban works by blocking a clotting protein called factor Xa, which is part of the clotting reaction. That is in contrast to other blood thinners, which work by preventing platelets from sticking together.
The drug is not available in the U.S., though Pfizer and Bristol-Myers plan to submit it to the Food and Drug Administration later this year. The companies are seeking approval to prevent stroke in patients with a type of heart defect.

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