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FUNGIFEX TABLET 250MG [SIN16925P]
Active ingredients: FUNGIFEX TABLET 250MG
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Product Info
FUNGIFEX TABLET 250MG
[SIN16925P]
Product information
Active Ingredient and Strength | TERBINAFINE HYDROCHLORIDE EQV TERBINAFINE - 250 MG |
Dosage Form | TABLET |
Manufacturer and Country | REMEDICA LTD - CYPRUS |
Registration Number | SIN16925P |
Licence Holder | GOLDPLUS UNIVERSAL PTE LTD |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | D01BA02 |
Indications
Treatment of:
Onychomycosis (fungal infection of the nail) caused by dermatophyte fungi.
Tinea capitis.
Fungal infections of the skin (Tinea corporis, Tinea cruris, Tinea pedis) and yeast infections of the skin caused by the genus Candida (e.g. Candida albicans) where oral therapy is generally considered appropriate owing to the site, severity or extent of the infection.
Oral terbinafine is not effective in Pityriasis versicolor (also known as Tinea versicolor).
Dosage and method of administration
Adults
250 mg once daily.
Skin infections
Recommended duration of treatment:
Tinea pedis (interdigital, plantar / moccasin type): 2 to 6 weeks
Tinea corporis, T. cruris: 2 to 4 weeks
Cutaneous candidiasis: 2 to 4 weeks.
Complete resolution of the signs and symptoms of infection may not occur until several weeks after mycological cure.
The duration of treatment varies according the indication and the severity of the infection.
Hair and scalp infections
Recommended duration of treatment:
Tinea capitis: 4 weeks.
Tinea capitis occurs primarily in children.
Onychomycosis
For most patients the duration of successful treatment is 6 to 12 weeks.
Fingernail onychomycosis
Six weeks of therapy is sufficient for fingernail infections in most cases.
Toenail onychomycosis
Twelve weeks of therapy is sufficient for toenail infections in most cases.
Some patients with poor nail outgrowth may require longer treatment. The optimal clinical effect is seen some months after mycological cure and cessation of treatment. This is related to the period required for outgrowth of healthy nail.
Special populations
Hepatic impairment
Terbinafine is containdicated for patients with chronic or active hepatic disease (see sections Contraindications and Special warnings and precautions for use – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Renal impairment
The use of terbinafine has not been adequately studied in patients with renal impairment and is therefore not recommended in this population (see section Special warnings and precautions for use and section Pharmacokinetic properties – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Geriatric Patients
There is no evidence to suggest that elderly patients (aged 65 years or above) require different dosages or experience different side effects than younger patients. When prescribing Fungifex for patients in this age group, the possibility of impairment of liver or kidney function should be considered (see Precautions – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Pediatric Patients
No data are available in children under two years of age (usually <12 kg).
Table caption
Children weighing | <20 kg | 62.5 mg | (half a 125 mg tablet) |
Children weighing | 20 to 40 kg | 125 mg | (one 125 mg tablet) |
Children weighing | >40 kg | 250 mg | (two 125 mg tablets) |
Method of administration
The scored tablets are taken orally with water. They should preferably be taken at the same time each day and can be taken on an empty stomach or after a meal.
Contraindications
Known hypersensitivity to terbinafine or to any of the excipients of Fungifex.
Chronic or active hepatic disease.
