Azilect, a Synopsis of Parkinson's Disease Treatment Option
FDA Approval of Azilect Provides Advancement in the Treatment of Parkinson's Disease
By Chrissy & Company, published Jun 05, 2006
Published Content: 3,215 Total Views: 1,625,732 Favorited By: 70 CPs
Parkinson’s Disease’s debilitating factors result from a degeneration of the brain cells which produce dopamine. Dopamine, found naturally in the body, is the brain chemical which aides in the communication path, between brain and body, to initiate and control movement in a normal fashion. Without dopamine, the brain and body do not communicate efficiently which results in various symptoms such as tremors, involuntary movements and irregular gait.
In an effort to further cure the symptoms of Parkinson’s Disease, Teve Pharmaceutical Industries, has developed a new drug, approved by the FDA, called Azilect. I Although,initially approved for use as a single drug therapy in the early stages of Parkinson’s Disease, it is now recommended as a combination therapy in patients with advanced Parkinson’s who currently take Levodopa. In treatment of Parkinson’s Disease, Azilect, when given once daily, has shown to improve function and, in 46 percent of the cases studied, no additional dopaminergic drug was required. When treated in the first six months, patients showed significantly less symptom progression than patients who were left untreated.
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Takeaways
- Azilect does not exhibit evidence of the "cheese" effect found in other medications.
- Azilect is approved for use in Parkinson's patients in Europe and is under FDA review
- Early use of Azilect will significantly decrease the progression of Parkinson's
Did You Know?
Azilect, in the treatment of Parkinson's Disease, reduced the daily "off" time by an average of 1.2 hours.
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