Patient Information Sheet This is a summary of the most important information about Razadyne. For details, talk to your healthcare professional. FDA ALERT [3/2005]: FDA and other international health authorities are reviewing the safety of Razadyne after data from two clinical studies indicated that people taking the drug had a higher death rate than those taking a placebo (sugar pill). Based on this information, FDA has asked the manufacturer to revise the labeling. Please ask your healthcare provider if Razadyne is right for you. This information reflects FDA’s preliminary analysis of data concerning this drug. FDA is considering, but has not reached a final conclusion about, this information. FDA intends to update this sheet when additional information or analyses become available. |
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What Is Razadyne? Razadyne is a medicine used to treat mild to moderate Alzheimer’s disease. Who Should Not Take Razadyne? You should NOT take Razadyne if you:
What Are The Risks? The most frequent side effects experienced in patients taking Razadyne were:
What Should I Tell My Healthcare Professional Before Taking Razadyne?
Are There Any Interactions With Drugs or Foods? Tell your healthcare professional about all the medicines you take, including prescription and over-the-counter drugs, and supplements. Your healthcare professional may have to adjust your dose or watch you more closely if you take any of the following medications:
How Do I Take Razadyne? Razadyne comes as a tablet and an oral solution to take by mouth. It is usually taken twice a day, preferably with the morning and evening meals. Your healthcare professional will start you on a low dose of Razadyne and gradually increase your dose over time, with a minimum of 4 weeks between each increase in dose. This helps to minimize the amount of side effects. Is There Anything Else I Need To Know? Razadyne may make you drowsy. Do not drive a car or operate machinery until you know how Razadyne affects you. Date created: March, 2005, updated August 9, 2006 |
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