
Product
Name :
Flixotide Accuhaler
(sold in the US as Flovent Diskus)
Product
Type :
fluticasone propionate
Packaging
and Product :
50mcg, 100 mcg,
250mcgs
Manufacturer :
GlaxoWellcome
Product
Classification :
Prescription
Medication
Why is it
prescribed?
Flovent® Diskus (Flixotide Accuhalers) contains fluticasone
propionate.
Fluticasone propionate is used to control the signs and
symptoms of asthma that are responsive to orally inhaled
corticosteroids. It is also used as a nasal spray to relieve
nasal congestion in the treatment of seasonal and perennial
rhinitis (runny nose) where inflammation of the lining of the
nose causes it to run.
Side Effects
Flovent® Diskus (Flixotide Accuhaler) contains fluticasone
propionate.
Every drug is capable of producing unwanted effects. Often,
fluticasone propionate users who use their medication properly,
never experience any unwanted effects. The severity and duration
of these effects are dependant on many factors including
duration of therapy, dose, route of administration and
individual response. Possible unwanted effects include:
sneezing attacks immediately after use (nasal spray only)
irritation and burning in the nose (nasal spray only)
localized infection of Candida Albicans (yeast) of the mouth
and throat
Less common:
sore throat (oral inhalation only)
hoarseness (oral inhalation only)
cough
headache
nausea
Rare:
immediate or delayed allergic reaction (e.g. rash, hives, and
bronchospasm)
flushing, itchiness, and swelling of the eyes, face, lips and
throat
Precautions and Warnings for Flovent® Diskus (Flixotide
Accuhaler)
Flovent® Diskus (Flixotide Accuhaler) contains fluticasone
propionate
Never use a higher dose than what you have been prescribed.
Using higher than recommended doses will cause greater
absorption by the body and possibly lead to greater occurrence
of unwanted effects. Optimal relief of symptoms may require 2 to
7 days of continuous therapy.
If symptoms do not improve or the condition worsens, the
doctor should be contacted.
Treatment with fluticasone should never be stopped without
first consulting your doctor.
Discontinuation of fluticasone requires gradual tapering or
you may experience a flare-up of your condition.
Inadequate response can often be a result of improper use of
the delivery device. Your doctor or pharmacist should instruct
you on the correct use of these preparations. Each product comes
with a package insert that should be read and then kept as a
reference.
Children using any of these preparations should do so under
the direct supervision of an adult who is familiar with it's
proper use.
It is important to inform subsequent physicians that you are
using or have used fluticasone propionate or any other
corticosteroids as this may vary the treatment plan.
When you have been treated with oral corticosteroids (e.g.
prednisone) for prolonged periods and are being transferred to
intranasally or orally inhaled fluticasone propionate, you may
experience withdrawal symptoms (e.g. joint and/or muscular pain
and depression). These symptoms should be reported to your
doctor, especially if you have associated asthma or another
condition in which too rapid a decrease in systemic steroids may
cause a severe flare-up of symptoms. Fluticasone propionate may
mask some signs of infection and new infections may appear. The
body tends to have a decreased resistance to localized
infections while on this therapy so anything of this nature
should be reported to the doctor. Drug Interactions: No specific
drug interaction studies have been performed. Due to very low
absorption at therapeutic doses, it is unlikely that there would
be any important interactions. However in people with
hypoprothrombinemia (deficiency of a clotting factor in the
blood resulting in an increased tendency to bleed), ASA ( e.g.
Aspirin ®) should be used cautiously.
Use is not recommended in the following situations:
allergy to fluticasone propionate or any component of the
preparation.
tuberculosis
untreated fungal, bacterial and viral infections
children under 4 years of age
Caution recommended in the following situations:
people previously treated for prolonged periods with oral
corticosteroids (e.g. prednisone)
Use in pregnancy: If you suspect that you might be pregnant,
consult your doctor. Use while breast-feeding: It is not known
whether fluticasone propionate is passed into breast milk, but
it is suspected. Consult your doctor or pharmacist before you
begin breast- feeding.
Directions for Use
The usual adult dose is 100 to 500 mcg twice a day depending
on the severity of the asthma and the patient's individual
response.
The usual dose for children 4 years of age or over is 50 to
100 mcg twice a day depending on the severity of the asthma and
the patient's individual response.
Lung Diseases Treated with this Drug
allergic rhinitis
allergies
asthma
hay fever
perennial rhinitis
rhinitis
runny nose
seasonal allergies
seasonal rhinitis
sinus infections
sinusitis
Need More Information?
For more information contact your physician, pharmacist,
other health care professional or for general questions call
your local lung association. |