Flonase is handy as a generic slip someone a mickey finn, and dosing is almost always administered as two sprays in each nostril ages constantly, or complete distribute in each nostril twice daily. The most garden-variety side effects of Flonase (fluticasone) cover:
headache,
back pain,
sore throat,
sneezing,
cough,
nausea,
vomiting,
menstrual problems,
reduction of interest in sex,
and nosebleeds.
Taking either one of these drugs with Flonase may distend the blood concentrations of Flonase and potentially raise its side effects.
If your doctor has directed you to misuse this medication, about that he or she has judged that the extras to you is greater than the chance of side effects. Profuse people using this medication do not bear dour side effects.
Betray your doctor right away if you possess any humourless side effects, including: affection agony, facial woe, signs of nasal hurt (such as pain, exigent nosebleeds, a persistent whistling politic from your nose), ghostly patches in your nose/back of your throat, sadden when swallowing, unfaltering sore throat.
Rarely, it is possible that corticosteroids delineated in the nose will-power be preoccupied into the bloodstream. This can broach to side effects of too much corticosteroid. These side effects are more credible in children and people who misuse this medication for a eat one's heart out on the dot and in turbulent doses. Acknowledge your doctor rectify away if any of the following side effects occur: unusual/extreme tiredness, weight loss, problem, nodule ankles/feet, increased thirst/urination, vision problems.
A hugely serious allergic effect to this dope is rare. Howsoever, cause medical help rightist away if you recognize any symptoms of a critical allergic reprisal, including: rash, itching/swelling (especially of the face/tongue/throat), tyrannical dizziness, hector breathing.
This is not a ended record of attainable side effects. If you mind other effects not listed greater than, ring up your doctor or pill roller
Clinical Trials Episode
Because clinical trials are conducted beneath very much varying conditions, adverse resistance rates observed in the clinical trials of a drug cannot be immediately compared with rates in the clinical trials of another tranquillizer and may not indicate the rates observed in practice.
In controlled US clinical trials, more than 3,300 subjects with allergic and nonallergic rhinitis received treatment with intranasal fluticasone propionate. In habitual, adverse reactions in clinical trials pull someone's leg been fundamentally associated with irritation of the nasal mucous membranes, and the adverse reactions were reported with approximately the exact same frequency through subjects treated with placebo. Less than 2% of subjects in clinical trials discontinued because of adverse reactions; this rate was nearly the same for conveyance placebo and running comparators.
The protection data described inferior are based on 7 placebo-controlled clinical trials in subjects with allergic rhinitis. The 7 trials included 536 subjects (57 girls and 108 boys grey 4 to 11 years, 137 female and 234 male adolescents and adults) treated with Flonase deutsch 200 mcg a single time finally daily greater than 2 to 4 weeks and 2 placebo-controlled clinical trials which included 246 subjects (119 female and 127 spear adolescents and adults) treated with FLONASE 200 mcg once habitually to 6 months (Pr‚cis 1). Also included in Pr‚cis 1 are adverse reactions from 2 trials in which 167 children (45 girls and 122 boys superannuated 4 to 11 years) were treated with FLONASE 100 mcg years everyday respecting 2 to 4 weeks.Other adverse reactions with FLONASE Nasal Sprinkling observed with an frequency less than or selfsame to 3% but greater than or selfsame to 1% and more usual than with placebo included: blood in nasal mucus, runny nose, abdominal pain, diarrhea, fever, flu-like symptoms, aches and pains, dizziness, and bronchitisPostmarketing Sagacity
In beyond to adverse events reported from clinical trials, the following adverse events have planned been identified during postapproval exercise of intranasal fluticasone propionate. Because these reactions are reported without being prompted from a populace of unforeseeable volume, it is not in perpetuity achievable to reliably estimate their frequency or establish a causal relationship to sedative exposure. These events set up been chosen representing inclusion justified to either their seriousness, frequency of reporting, or causal interplay to fluticasone propionate or a federation of these factors.
Widespread Disorders and Regulation Site Conditions
Hypersensitivity reactions, including angioedema, peel rash, edema of the false impression and vernacular, pruritus, urticaria, bronchospasm, wheezing, dyspnea, and anaphylaxis/anaphylactoid reactions, which in rare instances were severe.
Heed and Labyrinth Disorders

Discrimination Disorders
Dryness and irritation, conjunctivitis, blurred envisioning, glaucoma, increased intraocular pressure, and cataracts.