About Singulair:

Common Uses: This medicine is used for the prevention and long-term treatment of asthma. It is also used to treat hay fever (seasonal allergic rhinitis). Montelukast works by blocking substances in the body called leukotrienes. Blocking leukotrienes improves asthma and seasonal allergic rhinitis symptoms.

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Additional Information:

Generic Name: E: MONTELUKAST (mon-te-LOO-kast)

How to use this Medicine: Follow the directions for using this medicine provided by your doctor. This medicine may come with a patient leaflet. Read it carefully. Ask your doctor, nurse, or pharmacist any questions that you may have about this medicine. CHEW THOROUGHLY before swallowing. This medicine may be taken on an empty stomach or with food. Generally, if this medicine is being taken for asthma, it is taken once daily in the evening. If taking for hay fever (seasonal allergic rhinitis), take the medicine at about the same time each day (either morning or evening). If you are taking for both asthma and hay fever, take the medicine in the evening. STORE THIS MEDICINE at room temperature 77 degrees F (25 degrees C) in a tightly-closed container, away from heat, moisture, and light. Brief storage between 59 and 86 degrees F (15 and 30 degrees C) is permitted. CONTINUE TO TAKE THIS MEDICINE even if you feel well. Do not miss any doses. IF YOU MISS A DOSE OF THIS MEDICINE use it as soon as your remember. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. DO NOT take 2 doses at once.

Cautions: THIS MEDICINE WILL NOT STOP AN ASTHMA ATTACK once one has started. IF YOU ARE ALSO USING A BRONCHODILATOR INHALER, be sure to always carry the inhaler with you to use during asthma attacks. Consult your doctor or pharmacist for specific advice on all drug therapy. CONTACT YOUR DOCTOR IF YOUR SYMPTOMS DO NOT IMPROVE or if they become worse while you are using this medicine. If your short-acting inhaler use increases or if use exceeds the 24-hour maximum prescribed by the doctor. DO NOT STOP USING THIS MEDICINE or any other asthma medicine without first checking with your doctor. KEEP ALL DOCTOR AND LABORATORY APPOINTMENTS while you are using this medicine. Laboratory and/or medical tests should be performed periodically to monitor your progress or check for side effects. Check with your doctor for more information. BEFORE YOU BEGIN TAKING ANY NEW MEDICINE, either prescription or over-the-counter, check with your doctor or pharmacist. PHENYLKETONURICS: this medicine may contain aspartame, if you have phenylketonuria (PKU) or any other condition where you must restrict your intake of aspartame (or phenylalanine), consult your doctor or pharmacist regarding the safe use of this medicine. FOR WOMEN: IF YOU PLAN ON BECOMING PREGNANT, discuss with your doctor the benefits and risks of using this medicine during pregnancy. IT IS UNKNOWN IF THIS MEDICINE IS EXCRETED in breast milk. IF YOU ARE OR WILL BE BREAST-FEEDING while you are using this medicine, check with your doctor or pharmacist to discuss the risks to your baby.

Possible Side Effects: SIDE EFFECTS that may occur while taking this medicine include unusual weakness, stomach upset, diarrhea, dizziness, cough, headache, nausea, vomiting, trouble sleeping, or mouth pain. If they continue or are bothersome, contact your doctor. CONTACT YOUR DOCTOR IMMEDIATELY if you experience hallucinations, fever, persistent sore throat or earache, or flu symptoms. CONTACT YOUR DOCTOR IMMEDIATELY if you experience any of these highly unlikely but serious side effects including stomach pain, muscle aches/cramps, irregular heartbeat, yellowing eyes/skin, numbness/tingling of the hands or feet, easy bruising or bleeding, swelling, or seizures. AN ALLERGIC REACTION to this medicine is unlikely, but seek immediate medical attention if it occurs. Symptoms of an allergic reaction include rash, itching, severe swelling, severe dizziness, or trouble breathing. If you notice other effects not listed above, contact your doctor, nurse, or pharmacist.

Singulair

More about Singulair ...

Dosage and amounts subject to availability:
10 mg 20 tablets
4 mg 30 tablets

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FDA Warns on Black-Market IUDs : WASHINGTON -- Many intrauterine devices (IUDs) sold over the Internet from foreign pharmacies are not approved in the U.S. and are possibly dangerous, the FDA said. The agency said an investigation disclosed that patients in Rhode Island, Massachusetts, and Kentucky had received unapproved IUDs from healthcare providers who had bought them from foreign pharmacies, presumably to save money. In a "Dear Colleague" letter to providers, the FDA said it had uncovered distribution of "unapproved versions of FDA-approved products such as Mirena, Implanon, Copper-T, and ParaGard; as well as products not approved for use in the U.S., such as T-Safe." These products may not be as effective or safe as FDA-approved IUDs, the agency warned. Women who believe they may have received an unapproved IUD should use another contraceptive method and talk to their healthcare providers, the FDA recommended. The FDA also advised physicians to use extra caution when asked to insert IUDs provided by patients. Healthcare providers should verify that products are authentic FDA-approved devices and were purchased from a licensed U.S.-based supplier. The agency also noted that billing Medicaid or private insurers for unapproved medical products could bring criminal fraud charges. "To reduce the chance of receiving an unapproved or adulterated medical product, your Internet purchases should be made from state-licensed distributors or pharmacies located in the U.S.," the FDA said. It recommended buying only from Internet pharmacies displaying a logo from the National Association of Boards of Pharmacy, known as the VIPPS seal for Verified Internet Pharmacy Practice Sites. "Healthcare providers should be aware that purchasing medical products from websites that are outside of the U.S. may be illegal and may increase the risk of receiving a potentially harmful product, since many websites sell products that are not FDA approved and could be manufactured in other countries." The FDA first became aware of the problem in Rhode Island, but its probe turned up unapproved products in the two other states. The investigation is continuing, the agency said.

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