Fluticasone Propionate

Fluticasone Propionate is a synthetic corticosteroid with mainly glucocorticocoid activity. Fluticasone Propionate is used by oral inhalation for the prophylactic treatment of asthma. Fluticasone Propionate is reported to have a local effect on lungs without causing significant systemic effects, reduces airway inflammation and hence reduces oedema and secretions of mucous into the airway. It also is used as a nasal spray in the treatment of allergic rhinitis. When applied topically used in the treatment of various skin disorders. Fluticasone approved by FDA in december 1990


Adult Dose
Dose: 0.05%
Single Dose: 0.05 (0.05)
Frequency: 24 hourly
Route: Topical
Instructions: Frequency may be increased upto twice daily if needed.
Neonatal
Paedriatic
Characteristics
. It is of Synthetic origin and belongs to Corticosteroid. . The Molecular Weight of Fluticasone Propionate is 500.60. Its pKa is not ionizable.
Contraindications
Fluticasone Propionate is contraindicated in conditions like Acne vulgaris,Rosacea,Perioral dermatitis,Hypersensitivity,Primary cutaneous viral infection,Perianal and genital pruritis.
Effects
The severe or irreversible adverse effects of Fluticasone Propionate, which give rise to further complications include Glaucoma, Cataract, Growth retardation, Adrenocortical suppression, Decrease in bone mineral density.The symptomatic adverse reactions produced by Fluticasone Propionate are more or less tolerable and if they become severe, they can be treated symptomatically, these include Pruritus, Dysphonia, Allergic contact dermatitis, Cough, Oral candidiasis, Local burning, Hyperpigmentation, Hypertrichosis, Vocal cord myopathy, Throat irritation, Superficial blood vessels dilatation, Superficial blood vessels thinning, Secondary dermatitis, Hypercortisolism.
Indications
Fluticasone Propionate is primarily indicated in conditions like Allergic rhinitis, Asthma, Atopic eczema, Contact sensitivity reactions, Dermatitis, Discoid eczema, Discoid lupus erythematosus, Eczema, Infantile eczema, Neurodermatoses, Parennial rhinitis, Perennial rhinitis, Psoriasis, Purigo nodularis, Seborrheic dermatitis, and can also be given in adjunctive therapy as an alternative drug of choice in Generalised erythroderma, Insect bite reactions, Liver transplant.
Interactions
Fluticasone Propionate is known to interact with other drugs, the details of drug interactions is as follows:DrugDetailsSeverityOnsetManagementCarbamazepineCyclosporin AFrusemide or FurosemidePhenytoin (Na)PrimidoneRifampicinTheophyllineVORICONAZOLEVoriconazole may increase the serum concentration of fluticasone by decreasing its metabolism. monitor for changes in the therapeutic and adverse effects of fluticasone if voriconazole is initiated, discontinued or dose changed.Warfarin (Na) These interactions are sometimes beneficial and sometimes may pose threats to life. Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.
Interfrence
Risks
Drug should not be given to Pregnant Mothers, and Neonates.If prescribing authority justifies the benefits of the drug against the possible damages he/she should reevaluate them and consult the reference material and previous studies.
Storage
Inhaler, Nasal Spray, Cream, Oint. Store at room temperature, Below 30°C. Protect from Moisture and Heat.
Warnings
It should be used with caution in patients with active tuberculosis infection of respiratory tract or in untreated fungal, bacterial or systemic viral infections. Corticosteroids should only be used systemically with great caution in the presence of congestive heart failure (CHF), recent myocardial infraction (MI), hypertension, diabetes mellitus, epilepsy, glaucoma, hypothyroidism, liver failure, osteoporosis, peptic ulceration or renal impairment. Children may be at increase risk of some adverse effects, corticosteroid causes growth retardation and prolonged use is rarely justified. Live vaccine should not be given to patients receiving high dose systemic corticosteroid therapy nor for atleast 3 months afterwards, killed vaccine or toxoids may be given, although the response may be attenuated. During prolong treatment with corticosteroids, patients should be examined regularly, sodium intake may need to be reduced and calcium and potassium supplement may be necessary. Patient should carry cards given full details of their corticosteroid therapy. Avoid use during pregnancy. Use nasal steroids with caution until healing has occurred. Care should be taken when using corticosteroid topically to ensure the amount applied is the inimum that provides therapeutic benefit. When applied to eyelids, care is needed to ensure that the preparation does not enter the eye so as to avoid the risk of local irritation or gluacoma. Appropriate antimicrobial therapy should be used whenever treating inflammatory lesions which have become infected. Any spread of infection requires withdrawal of topical corticosteroid therapy and systemic administration of antimicrobial agents.
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