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Advair (Fluticasone)

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Advair is used to treat certain growths in the nose (nasal polyps). It belongs to a class of drugs known as corticosteroids. Advair works by reducing swelling in the nasal passages. This can help decrease symptoms such as stuffy nose.

Other names for this medication:
Advair, Alerflo, Cazon, Emderm, Fexin, Flocare, Floease, Flohale, Flomale, Flomist, Flovent, Fluderm, Fluster, Flutec, Fluticare, Fluticasone, Fluticone, Flutiflo, Flutilab, Flutiriv, Flutivate, Flutopic, Flutrol, Formosone, Ftica, Furamist, Furaspray, Geflute, Moliderm, Nazomac, Otrivin, Rhinofit, Sylone, Ultisone, Ventiflo, Zoflut

Similar Products:
Avapro, Provera, Aricept, Albenza, Rocaltrol, Elavil, Procid, Exprex, Farlev, Trimoxsul, Nidipine,

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Also known as: Fluticasone


Fluticasone nasal spray is used to treat sneezing, itchy or runny nose, or other symptoms caused by hay fever. It is also used to treat nasal polyps in adults. This is a steroid medicine.

This medicine is available both over-the-counter (OTC) and with your doctor's prescription.


This section provides information on the proper use of a number of products that contain fluticasone. It may not be specific to Advair. Please read with care.

This medicine comes with patient instructions. Read and follow these instructions carefully. Ask your doctor or pharmacist if you have any questions.

This medicine is for use only in the nose. Do not get any of it in your eyes or on your skin. If it does get on these areas, rinse it off right away.

To use the fluticasone propionate and Veramyst® nasal spray:

When you use the fluticasone nasal spray for the first time, you must prime the spray. Press down fully the top of the pump 6 times or until a fine spray comes out. Prime the spray if it has not been used for more than 7 days (fluticasone propionate) or 30 days (Veramyst®) or if the cap has been left off the bottle for 5 days or longer. Shake the medicine well before each use. Gently blow your nose before using the spray. Tilt your head back slightly and insert the tip of the nose piece into your nostril. Close the opposite nostril with a finger. Release 1 spray and at the same time, breathe in gently through the nostril. Hold your breath for a few seconds then breathe out slowly through your mouth. Spray the opposite nostril using the same steps. Do not blow your nose or tip your head back after using the spray. Wipe the tip of the outside of the nose piece with a clean, dry tissue or cloth and put the cap back on. Throw this medicine away after you use 120 sprays.

To use the Xhance™ nasal spray:

Prime the new spray before using it for the first time. To prime, gently shake the bottle then spray 7 times into the air away from the face, or until some medicine comes out. If you have not used this medicine for 7 days or longer, prime it again by shaking and spraying 2 times into the air, away from the face. Shake the medicine well before each use. Insert the tip of the cone-shaped nosepiece deep into the nose to create a seal between the nosepiece and the nostril. Place the mouthpiece inside your mouth and blow on it. While blowing, push the bottle up to actuate the spray pump. Continue to blow through your mouth until the medicine is released, but do not inhale or exhale through the nose. Repeat in the other nostril for a full dose.

You may need to use this medicine for a few days before you start to feel better.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For nasal polyps: For nasal dosage form (spray): Xhance™: Adults—At first, 1 spray (93 micrograms [mcg]) fluticasone in each nostril two times a day. Some patients may need 2 sprays in each nostril two times a day. Your doctor may adjust your dose as needed. Children—Use and dose must be determined by your doctor. For symptoms of hay fever: For nasal dosage form (spray): Fluticasone propionate: Adults—At first, 2 sprays in each nostril once a day. Some patients may need 1 spray in each nostril two times a day (morning and evening). Your doctor may adjust your dose as needed. Children 4 years of age and older—At first, 1 spray in each nostril once a day. Some patients may need 200 mcg or 2 sprays in each nostril once a day. Children younger than 4 years of age—Use is not recommended. Veramyst®: Adults and children 12 years of age and older—At first, 2 sprays in each nostril once a day. Your doctor may decrease your dose to 55 mcg or 1 spray in each nostril once a day. Children 2 to 11 years of age—At first, 1 spray in each nostril once a day. Your child's doctor may need to increase the dose up to 2 sprays in each nostril once a day depending on your child's condition. Children younger than 2 years of age—Use and dose must be determined by your doctor.


An overdose of Advair is not expected to produce life-threatening symptoms. However, long-term use of high steroid doses can lead to symptoms such as thinning skin, easy bruising, changes in the shape or location of body fat (especially in your face, neck, back, and waist), increased acne or facial hair, menstrual problems, impotence, or loss of interest in sex.


Store at a room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw the medication away after you have used 120 sprays, even if there is still medicine left in the bottle. Keep out of the reach of children.

Side effects

The most common side effects associated with Advair are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of fluticasone nasal spray in children. However, safety and efficacy of Veramyst® nasal spray have not been established in children younger than 2 years of age, and fluticasone propionate nasal spray in children younger than 4 years of age.

Appropriate studies have not been performed on the relationship of age to the effects of Xhance™ nasal spray in the pediatric population. Safety and efficacy have not been established.

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In contrast to reductive activation, upon acid dilantin dosage degradation of a diacetoxymitosene the C-1 group appeared to be lost faster. Role of intravenous levetiracetam in acute seizure management of children. An application of information science and technology to provision of rehabilitation services. Eligible infants had mothers who had prenatal ultrasound screening. Thirteen patients showed mutations in POMT1 and five harboured mutations in POMT2, accounting for a total of 20 different mutations, eight of which were novel (two in POMT1 and six in POMT2). Treatment for CIS with IFNbeta is effective in delaying conversion to clinically definite multiple sclerosis.

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Hemolymph fractions from Mytilus exerted a reciprocal toxic effect on the bacteria. Particularly, diagnosis and prognosis need to be rethought in a model to suit the condition of COPD. Histone modifications include acetylation, phosphorylation, and methylation, resulting in a combination of histone marks known collectively as the histone code. The model was tested comparing the predicted and the observed pharmacokinetics of 45 molecules. Transmission of tetanus antibodies with the colostrum to newborn foal and subsequent active immunization. Cocaine was evaluated with regard to D(2)R binding using a human D(2L)R stable expressing CHO cell line and was found to produce an increase in the affinity of hD(2L)R for DA. Active and passive release of blood from canine spleen and small intestine. Mechanical forces regulate focal adhesion and costamere assembly in cardiac myocytes. Angiotensin II-based hypertension and the sympathetic nervous system: the role of dose and increased dietary salt in rabbits. To test the hypothesis that joint hypermobility may play a part in the pathogenesis of pain in fibromyalgia, schoolchildren were examined for the coexistence of joint hypermobility and fibromyalgia.

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However, these mothers, with support, responded with a reduction in their abusive actions. A broadband Fourier transform microwave spectrometer based on chirped pulse excitation. From DNA duplex thermal stability experiments assayed with the S1 endonuclease, there is preliminary evidence that well-matched sequences identified by the enzyme are not similarly recognized by HA. No inpatients tested showed any symptoms of typical adenoviral conjunctivitis, but slight conjunctival infection caused by postoperative reaction and/or mild conjunctivitis that did not resemble HAdV infection was observed. By measuring ligand-induced DNA elongation at different ligand concentrations, we determined the binding constant ultram breastfeeding and site size as a function of force. Adult C57Bl/6 mice were subjected to a 90-min middle cerebral artery occlusion (MCAO). The aim of the present study was to examine whether RAD001 (everolimus) can selectively suppress the proliferation of different anaplastic thyroid cancer (ATC) cells. Vitality and genetic fidelity of white-rot fungi mycelia following different methods of preservation. Most patients are in their late teens and early twenties, and in young women self-poisoning is the most common cause of emergency admission to a medical ward.

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The accidental discovery of a retrotracheal left pulmonary artery in a 4-month-old infant encouraged us to review the various embryologic theories concerning this very rare anomaly and perform an anatomic update in order to better define surgical treatment. Adequacy of dietary intake declines with age in children with sickle cell disease. Compared to control, either nimesulide or niflumic acid significantly inhibited the ovulation in the superovulated rats. The apparent proportion of MAO-A to MAO-B activities in the gerbil liver was approximately 6:4, whereas MAO-A in the frontal cortex of the gerbil was exclusively predominant, consistent with the previous data in the golden hamster which belongs to the same family as the gerbil. Sputum and serum were collected at the start and end of anti-biotic therapy.

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The CT stage and tumour diameter were compared to the pathological stage. Cluster analysis was used to enhance understanding of heterogeneity in social adjustment of physically abused children. The membrane bound adenylate cyclase (ATP pyrophosphate-lyase (cyclizing) EC of the ciliate Tetrahymena pyriformis could be extracted by washing the membrane fraction with 0.25 M sucrose. There has been little examination on how this affects the quality of life of this group of patients and how they compare with other patients who have venous ulcers. We used concentration indices to provide a summary measure of disparities by income in potential years of life lost (PYLL) for the Hong Kong population from 1976 to 2006. Laboratory analysis of petrol, kerosene and engine oils, clearly established their lethal activities on resistant strains of Anopheles larvae. The experimental factors underlying this analysis were then studied using digitized images of corneal endothelial cells. Campus archives have provided physical, psychological, and social data on some 57,500 men and women who were born between 1896 and 1934, and who entered Harvard College or the University of Pennsylvania between 1916 and 1950, generally at age 17-20 years. Increasing back pain and prograf medication liver transplant progressive destruction with sclerosis of the involved vertebrae led to a needle biopsy examination of the vertebrae which showed evidence of chronic osteomyelitis and grew P aeruginosa on culture. The authors give a review of patients with bacterial cardiac disease treated in the Paediatric Clinic of Karl-Marx-University Leipzig between 1971 and 1987.

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