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Concise Prescribing Info
Contents
Betamethasone dipropionate 0.064% w/w, gentamicin sulphate 0.17% w/w
Indications/Uses
Impetigo, erythema & other localised primary bacterial skin infection w/ gm -ve component. Secondary bacterial infections complicating other pre-existing dermatoses.
Dosage/Direction for Use
Apply to the affected area bd.
Overdosage
View Beprogent overdosage for action to be taken in the event of an overdose.
Contraindications
Hypersensitivity.
Warnings
For additional cautionary notes to warn of the potential risk of using the medicine... Click to view Beprogent detailed prescribing information
Special Precautions
Discontinue use if irritation, sensitivity or other reaction develop & institute appropriate treatment. Can be absorbed in sufficient amounts producing systemic effects (eg, hypothalamic-pituitary-adrenal axis suppression, manifestation of Cushing’s syndrome, hyperglycaemia, glucosuria). Take precautions during prolonged treatment, when treating extensive body surface areas, when using occlusive technique & when treating childn. Prolonged use may result in overgrowth of non-susceptible organisms including fungi. Pregnancy & lactation.
Adverse Reactions
Betamethasone dipropionate: Burning sensation, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, maceration of the skin, secondary infection, skin atrophy, striae, miliria. Gentamicin sulphate: Ototoxicity, nephrotoxicity, hypersensitivity reactions.
Storage
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Description
View Beprogent description for details of the chemical structure and excipients (inactive components).
Action
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MIMS Class
ATC Classification
D07CC01 - betamethasone and antibiotics ; Belongs to the class of potent (group III) corticosteroids, in combination with antibiotics. Used in the treatment of dermatological diseases.
P1S1S3, A
Presentation/Packing
Form
Beprogent cream
Packing/Price
15 g x 1's;450 g x 1's
