Drug Uses
Allegra is indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children 6 years of age and older. Symptoms treated effectively were sneezing, rhinorrhea, itchy nose/palate/throat, itchy/watery/red eyes.

How Taken
Allegra is formulated as a capsule or tablet for oral administration. Allegra is usually taken twice a day, in the morning and the evening. Follow your doctor's instructions. Take each dose with a full glass of water.

Warnings/Precautions
Do not take Allegra if you have ever had an allergic reaction to it. Before taking this medication, tell your doctor if you have any serious illness such as heart, kidney, or liver disease. You may require a dosage adjustment or special monitoring during treatment if you have other illnesses. Allegra is in the FDA pregnancy category C. This means that it is not known whether Allegra will harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant. It is also not known whether Allegra passes into breast milk. Do not take Allegra without first talking to your doctor if you are breast-feeding a baby. Allegra is not approved for use by children younger than 6 years of age.

Missed Dose
If you miss a dose, use it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not "double-up" the dose to catch up.

Possible Side Effects
Stop taking Allegra and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives). Allergic reactions occur only rarely, and other serious side effects are not likely to occur. Some less serious side effects may be more likely to occur. Continue to take Allegra and talk to your doctor if you experience nausea or an upset stomach. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Storage
Store Allegra capsules and tablets at controlled room temperature 20-25?C (68-77?F). Foil-backed blister packs containing Allegra capsules and all tablet packaging should be protected from excessive moisture.

Overdose
Symptoms and signs of Allegra overdose are: dizziness, drowsiness, and dry mouth. Seek emergency medical attention.

More Information
Tell your doctor of all nonprescription and prescription medication you may use, especially: MAO inhibitors, certain blood pressure drugs, digoxin, and all adrenaline-like drugs. Report other drugs which affect the heart rhythm. Ask your doctor or pharmacist for more details. Check the labels carefully on all nonprescription products, such as cough-and-cold medicines that contain antihistamines and decongestants. Consult your pharmacist. Do not take Allegra for several days before any allergy testing since test results can be affected. Do not start or stop any medicine without doctor or pharmacist approval.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Allegra-D is indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children 12 years of age and older. Symptoms treated effectively include sneezing, rhinorrhea, itchy nose/palate/ and/or throat, itchy/watery/red eyes, and nasal congestion.

How Taken
The recommended dose of Allegra-D is one tablet twice daily for adults and children 12 years of age and older. It is recommended that the administration of Allegra-D with food should be avoided. A dose of one tablet once daily is recommended as the starting dose in patients with decreased renal function.

Warnings/Precautions
Do not take Allegra-D if you have taken a monoamine oxidase inhibitor (MAOI) in the last 14 days; asthma or another lung disease; diabetes; thyroid problems; glaucoma or increased pressure in the eye; urinary retention or an enlarged prostate; kidney or liver disease; or heart disease, high blood pressure, or an irregular heartbeat. You may not be able to take Allegra-D, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above. Allegra-D is in the FDA pregnancy category C. This means that it is not known whether it will be harmful to an unborn baby. Do not take Allegra-D without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known if Allegra-D passes into breast milk. Do not take Allegra-D without first talking to your doctor if you are breast-feeding a baby. Allegra-D is not approved for use by children younger than 12 years of age.

Missed Dose
If you miss a dose, use it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not "double-up" the dose to catch up.

Possible Side Effects
Nausea, stomach upset, trouble sleeping, headache, or cold symptoms may occur. If these persist or worsen, notify your doctor promptly. Unlikely but report promptly: dizziness, mental/mood changes, fast heartbeat, fever. Tell your doctor immediately if any of these highly unlikely but very serious side effects occur: fainting, irregular heartbeat. Although drowsiness is very uncommon at usual doses under normal circumstances, be aware that drowsiness may occur and may affect the ability to perform tasks requiring alertness (e.g., driving). If you notice other effects not listed above, contact your doctor or pharmacist.

Storage
Store at room temperature between 68 and 77 degrees F (20-25 degrees C) away from sunlight and moisture.

Overdose
In large doses, Allegra-D may give rise to giddiness, headache, nausea, vomiting, sweating, thirst, tachycardia, precordial pain, palpitations, difficulty in micturition, muscular weakness and tenseness, anxiety, restlessness, and insomnia. You can present a toxic psychosis with delusions and hallucinations or you may develop cardiac arrhythmias, circulatory collapse, convulsions, coma, and respiratory failure.

More Information
Use caution when driving, operating machinery, or performing other hazardous activities. Allegra-D may cause dizziness. If you experience dizziness, avoid these activities. Do not take Allegra-D close to a dose of an antacid that contains aluminum or magnesium. These antacids may decrease the effects of Allegra-D.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Clarinex is an antihistamine used to relieve the symptoms of hay fever (seasonal allergic rhinitis). Clarinex contains a long-acting tricyclic histamine antagonist with selective H1-receptor histamine antagonist activity.

How Taken
Clarinex comes in tablets to take by mouth. It can be taken with or without food and is usually taken once daily. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Clarinex exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Warnings/Precautions
Before taking Clarinex, tell your doctor if you have ever had an allergic reaction to an antihistamine; kidney disease; or liver disease. You may not be able to take Clarinex, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above. Clarinex is in the FDA pregnancy category C. This means that it is not known whether Clarinex will be harmful to an unborn baby. Do not take Clarinex without first talking to your doctor if you are pregnant or could become pregnant during treatment. Clarinex passes into breast milk and may affect a nursing infant. Do not take Clarinex without first talking to your doctor if you are breast-feeding a baby.

Missed Dose
If you miss a dose take it as soon as you remember. If it is almost time for your next dose, skip the one you missed and go back to your regular schedule. Never take 2 doses at the same time.

Possible Side Effects
Side effects cannot be anticipated. If any develop or change in intensity, inform your doctor as soon as possible. Only your doctor can determine if it is safe for you to continue taking Clarinex.More common side effects may include: dry mouth, fatigue, sleepiness, sore throat.Less common side effects may include: dizziness, dry throat, flu-like symptoms, muscle pain, nausea.Rare side effects may include: acute allergic reaction, hives, itching, rapid heartbeat, rash, shortness of breath, swelling.

Storage
Store at room temperature. Protect from heat. Keep this medication in the container it came in, tightly closed, and out of reach of children.

Overdose
Little is known about the effects of a Clarinex overdose. However, any medication taken in excess can have serious consequences. If you suspect an overdose, seek medical attention immediately. Symptoms of Clarinex overdose may include: rapid heartbeat, sleepiness.

More Information
Use caution when driving, operating machinery, or performing other hazardous activities. Although unlikely, Clarinex may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Flonase can relieve multiple nasal symptoms of congestion, sneezing, and itchy, runny nose. Flonase Nasal Spray is for topical administration to the nasal mucosa by means of a metering, atomizing spray pump.

How Taken
To get the best results with Flonase, you should use it regularly, as prescribed by your doctor, since its effectiveness depends on regular use. Because Flonase helps relieve inflammation, once you begin treatment you should use it once a day, every day as directed by your healthcare professional. The recommended starting dosage in adults is 2 sprays (50 mcg of Flonase Nasal Spray propionate each) in each nostril once daily (total daily dose, 200 mcg). The same dosage divided into 100 mcg given twice daily (e.g., 8 a.m. and 8 p.m.) is also effective. After the first few days, patients may be able to reduce their dosage to 100 mcg (1 spray in each nostril) once daily for maintenance therapy. Some patients (12 years of age and older) with seasonal allergic rhinitis may find as-needed use of 200 mcg once daily effective for symptom control. Greater symptom control may be achieved with scheduled regular use.

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 your system can inhibit your body's ability to fight off infections. You may not be able to use Flonase Nasal Spray nasal if you have an infection. Flonase Nasal Spray is in the FDA pregnancy category C. This means that it is not known whether Flonase Nasal Spray nasal will harm an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant. It is not known whether Flonase Nasal Spray passes into breast milk. Do not use Flonase Nasal Spray nasal without first talking to your doctor if you are breast-feeding a baby. Flonase Nasal Spray nasal is not approved for use by children younger than 4 years of age.

Missed Dose
Use the missed dose as soon as remembered unless it is almost time for the next dose. If so, skip the missed dose and resume your regular dosing schedule. Do not "double-up" the doses to catch up.

Possible Side Effects
Serious side effects from Flonase Nasal Spray nasal are not likely to occur. Stop using Flonase Nasal Spray nasal and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives). Other, less serious side effects may be more likely to occur. Continue to use Flonase Nasal Spray nasal and talk to your doctor if you experience stinging or burning of the nose; sneezing after application; yeast infection in the nose or throat (white patches); bleeding nose; perforated septum (inside left of nose); increased pressure in the eyes, glaucoma, or tearing of the eyes; headache or lightheadedness; nausea; cough; asthma symptoms; nasal stuffiness or a runny nose; or unpleasant (or loss of) taste or smell. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Storage
Store between 4? and 30?C (39? and 86?F). Keep your nasal spray out of the reach of children. Do not use your Flonase Nasal Spray after the date shown as "EXP" on the label or box.

Overdose
An overdose of this medication is not likely to occur. If you do think that an overdose has occurred, call an emergency room or poison control left.

More Information
Avoid items or activities that you know are allergens for you if they make your symptoms worse. Clean areas where dust or pet fur may aggravate your condition. Avoid exposing yourself to known sources of infection. Stay away from people with chicken pox, measles, or any other type of infection. Your immune system may not be strong enough to fight off an infection while you are using Flonase Nasal Spray nasal.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
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 use by children younger than 6 years of age. Nasacort Nasal Spray is not approved for use by children 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.

Storage
Store at Controlled Room Temperature, 20 to 25?C (68 to 77?F) away from sunlight and moisture. Avoid freezing. Keep out of reach of children.

Overdose
An overdose of this medication is not likely to occur. If you do think that an overdose has occurred, call an emergency room or poison control left for advice.

More Information
Avoid items or activities that are known allergens to you. Clean areas where dust or pet fur may aggravate your condition. Avoid exposing yourself to known sources of infection. Stay away from people with chicken pox, measles, or any other type of infection. Your immune system may not be strong enough to fight off an infection while using Nasacort.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Nasonex is a nasal allergy spray for the treatment of seasonal and perennial allergy symptoms. Nasonex helps relieve itchy, runny noses, sneezing and congestion caused by dust mites, pet dander and tree and grass pollen. Nasonex Nasal Spray is a corticosteroid demonstrating anti-inflammatory properties. The Corticosteroids have been shown to have a wide range of effects on multiple cell types.

How Taken
Shake Nasonex well before each use. Prime the spray pump as instructed by your pharmacist. Use as directed, generally two sprays in each nostril daily. Do not use this drug more often or longer than prescribed. Use Nasonex regularly during the prescribed treatment period for full benefit. If the drug is used for seasonal allergy, therapy is best started 2-4 weeks before the season. Improvement in symptoms occurs generally within 2 days and full benefit occurs after 1-2 weeks of use.

Warnings/Precautions
Before using Nasonex, tell your doctor and pharmacist if you have a viral, bacterial, or fungal infection of any kind. The absorption of this drug into your system can inhibit your body's ability to fight off infections. You may not be able to use Nasonex if you have an infection. Before using Nasonex, tell your doctor if you have a nasal septum ulcer, recently had nasal surgery, or nasal damage. You may not be able to use Nasonex, or you may require a dosage adjustment or special monitoring during your treatment. Nasonex is in the FDA pregnancy category C. This means that it is not known whether Nasonex will harm an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant. It is unknown whether Nasonex passes into breast milk. Do not use Nasonex without first talking to your doctor if you are breast feeding a baby. Nasonex is not approved for use by children younger than 3 years of age.

Missed Dose
If you miss a dose of Nasonex, use it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not "double-up" the dose to catch up.

Possible Side Effects
Headache or sore throat might occur. If these effects persist or worsen, notify your doctor promptly. Very unlikely but report promptly: vision changes, unusual nasal bleeding or irritation/pain, blood-tinged mucus/phlegm, unusual increase in thirst or urination, nausea, weakness, weight loss. In the unlikely event you have an allergic reaction to Nasonex, seek immediate medical attention. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist.

Storage
Store at 25?C (77?F); excursions permitted to 15-30?C (59-86?F). Protect from light. When Nasonex Nasal Spray, 50 mcg is removed from its cardboard container, prolonged exposure of the product to direct light should be avoided. Brief exposure to light, as with normal use, is acceptable.

Overdose
An overdose of this medication is not likely to occur. If you do think that an overdose has occurred, call an emergency room or poison control left.

More Information
Avoid items or activities that you know are allergens for you if they make your symptoms worse. Clean areas where dust or pet fur may aggravate your condition. Avoid exposing yourself to known sources of infection. Stay away from people with chicken pox, measles, or any other type of infectious disease. Your immune system may not be strong enough to fight off an infection while you are using Nasonex.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Patanol is a prescription medication that you can use to stop the affects off allergies in your daily life. Patanol is a liquid drop that you use in your eyes to keep your eyes from itching because of the allergies that you suffer from. Itchy eyes can cause redness, which will go away as you quit rubbing your eyes and your eyes are not itchy anymore because you are using Patanol.

How Taken
The recommended dose is one drop in each affected eye two times per day at an interval of 6 to 8 hours.

Warnings/Precautions
Do not use Patanol if you have a bacterial, viral, or fungal infection in your eye unless you are also receiving proper anti-infective treatment. Patanol is in the FDA pregnancy category C. This means that it is not known whether Patanol will harm an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant. It is not known whether Patanol passes into breast milk. Do not use Patanol without first talking to your doctor if you are breast-feeding a baby. Patanol is not approved by the FDA for use by children younger than 3 years of age.

Missed Dose
Take the missed dose as soon as you remember it.

Possible Side Effects
Serious side effects from Patanol are not likely to occur. Seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives). Less serious side effects may be more likely to occur. Continue to use Patanol and talk to your doctor if you experience burning, stinging, irritation, itching, redness, or dryness of the eyes; swollen eyelids; a stuffy or runny nose; headache; or changes in taste. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Storage
Store at 39?F to 86?F (4?C to 30?C).

Overdose
An overdose of this medication is unlikely to occur. If you do suspect an overdose, call an emergency room or poison control left near you. If the drops have been ingested (taken by mouth), drink plenty of fluid and call an emergency left for advice.

More Information
Do not touch the dropper to any surface, including your eyes or hands. The dropper is sterile. If it becomes contaminated, it could cause an infection in your eye. Patanol contains a preservative (benzalkonium chloride), so do not wear contact lenses while applying this medication. Contact lenses can be inserted about 15 minutes after a dose. Avoid other eye drops unless your doctor approves.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.       

Drug Uses
Zyrtec is an antihistamine. Antihistamines prevent sneezing, runny nose, itching and watering of the eyes, and other allergic symptoms. Zyrtec is used to treat allergies, hives (urticaria), and other allergic inflammatory conditions.

How Taken
Zyrtec comes as a tablet to take by mouth. It usually is taken once a day. It may be taken regularly or when allergy symptoms flare up. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Zyrtec exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor. Zyrtec may cause an upset stomach. Take Zyrtec with food or milk.

Warnings/Precautions
Before taking this medication, tell your doctor if you have kidney or liver disease. You may need a lower dose or special monitoring during your therapy with Zyrtec. Zyrtec is in the FDA pregnancy category B. This means that it is unlikely to harm an unborn baby. Do not take Zyrtec without first talking to your doctor if you are pregnant. Zyrtec passes into breast milk and may affect a nursing baby. Do not take Zyrtec without first talking to your doctor if you are breast-feeding a baby. If you are over 60 years of age, you may be more likely to experience side effects from Zyrtec. You may require a lower dose of this medication.

Missed Dose
If you forget to take a dose, do not take an extra tablet to catch up for the dose you forgot. Wait and take your next tablet at the regular time. Do not take more tablets than your doctor prescribed.

Possible Side Effects
Stop taking Zyrtec and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives). Other, less serious side effects may be more likely to occur. Continue to take Zyrtec and talk to your doctor if you experience sleepiness, fatigue, or dizziness; headache; or dry mouth. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Storage
Store at 20-25?C (68-77?F); excursions permitted to 15-30?C (59-86?F).

Overdose
Seek emergency medical attention. Symptoms of a Zyrtec overdose are not well known, but extreme sleepiness, confusion, and weakness may be expected.

More Information
Use caution when driving, operating machinery, or performing other hazardous activities. Zyrtec may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while you are taking Zyrtec.

Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.