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Arava Leflunomide is a disease-modifying antirheumatic drug that is prescribed to help manage active rheumatoid arthritis. Approved Uses; Arava has received FDA approval for treating adults with moderate to severe arthritis and psoriatic arthritis. It has been particularly effective in reducing swelling and alleviating pain. Limitations, on Usage; However it is important to note that Arava should not be administered in cases of liver dysfunction, leukopenia or when certain other contraindications are present. There are some suggestions from studies that Arava may be effective in treating conditions, like lupus although its important to note that these uses are not approved by the FDA.


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Do not take leflunomide if you are pregnant or plan to become pregnant. Leflunomide may harm the fetus. You should not begin taking leflunomide until you have taken a pregnancy test with negative results and your doctor tells you that you are not pregnant. You must use an effective method of birth control before you begin taking leflunomide, during your treatment with leflunomide, and for 2 years after treatment. Talk to your doctor if you plan to become pregnant within 2 years after stopping treatment with leflunomide. Your doctor can prescribe a treatment that will help to remove this medication more quickly from your body.


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It's also known by its brand name Arava. It may take four to six weeks before you start to feel the effects of leflunomide on your symptoms.


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  • Do not drink alcohol whilst you are taking leflunomide - it will increase the risk of damage to your liver.
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Leflunomide Arava is a drug approved to treat adult moderate to severe rheumatoid arthritis along with other rheumatic diseases. It suppresses the immune system to reduce inflammation that causes pain and swelling.

 

These medications may be counterfeit and potentially unsafe. Ask your health care provider for advice if you are unsure about the online purchase of any medication. Drug Exclusivity Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from days to seven years depending upon the circumstance of the exclusivity grant. AB Products meeting necessary bioequivalence requirements. Multisource drug products listed under the same heading i.

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