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NASACORT AQ       

      Nasacort is FDA approved for the treatment of the nasal symptoms of seasonal and year round allergies such as nasal congestion, itchy runny nose, and sneezing. Nasacort Nasal Spray is an unscented, thixotropic, water-based metered-dose pump spray formulation unit containing a microcrystalline suspension of triamcinolone acetonide in an aqueous medium.

How Taken
Nasacort Nasal Spray comes as a solution to inhale through the nose. It usually is inhaled one to four times a day at evenly spaced intervals. Before using triamcinolone, gently blow your nose to clear your nasal passages. Avoid blowing your nose for 15 minutes after inhaling the prescribed dose.

Warnings/Precautions
Before using this medication, tell your doctor if you have a viral, bacterial, or fungal infection of any kind. The absorption of this drug into the system can inhibit the body's ability to fight off infections. You may not be able to use Nasacort Nasal Spray if you have an infection. Nasacort Nasal Spray is in the FDA pregnancy C. This means that it is not known whether Nasacort Nasal Spray will be harmful to an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether Nasacort Nasal Spray passes into breast milk. Do not use Nasacort Nasal Spray without first talking to your doctor if you are breast-feeding a baby. Nasacort Nasal Spray is not approved for children use younger than 12 years of age.

Missed Dose
If you miss a dose of Nasacort, use it as soon as remembered; do not use if it is almost time for the next dose, instead, skip the missed dose and resume your usual dosing schedule. Do not "double-up" the dose to catch up.

Possible Side Effects
Nasacort may cause irritation, stinging, burning, or dryness of the nasal passages. Sneezing, nosebleed, headache, lightheadedness, loss of taste, throat irritation or nausea may also occur. If these effects continue or become bothersome, inform your doctor. Unlikely but report promptly: persistent nose or throat irritation/soreness, white patchy areas. Very unlikely but report promptly: broken or damaged nasal membranes, unusual weakness, weight loss, nausea/vomiting, fainting, dizziness, vision changes. If you notice other effects not listed above, contact your doctor or pharmacist.

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         Stimulation of a cranial nerve through an implant can effectively treat some children with epilepsy, according to the results of a new two-year study. In a study of more than 75 young patients, doctors found that 59 percent of those implanted with a vagus nerve stimulator did not suffer from localization-related epilepsy, or seizures occurring in one part of the brain. Hospital visits for epilepsy-related conditions also decreased by 41 percent, the researchers reported Wednesday at the International League Against Epilepsy Congress in Paris. The nerve stimulator is implanted in the left side of a patient's neck and works by sending signals to the brain to decrease the electrical activity that leads to seizures. It was approved by the U.S. Food and Drug Administration in 1997 for the treatment of epilepsy unresponsive to medication.
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