- Approval Id
- 6d72dd5aef578bbe
- Drug Name
- FUNGIFEX TABLET 250MG
- Product Name
- FUNGIFEX TABLET 250MG
- Approval Number
- SIN16925P
- Approval Date
- 2024-01-05
- Registrant
- GOLDPLUS UNIVERSAL PTE LTD
- Licence Holder
- GOLDPLUS UNIVERSAL PTE LTD
- Drug Type
- Therapeutic
- Forensic Classification
- Prescription Only
- Dosage Form
- TABLET
- Dosage
- **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).
Children weighing<20 kg62.5 mg(half a 125 mg tablet)
once dailyChildren weighing20 to 40 kg125 mg(one 125 mg tablet)
once dailyChildren weighing>40 kg250 mg(two 125 mg tablets)
once daily
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.
- Route Of Administration
- ORAL
- Indication Info
- **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).
- Contraindications
- **Contraindications**
- Known hypersensitivity to terbinafine or to any of the excipients of Fungifex.
- Chronic or active hepatic disease.
- Atc Code
- D01BA02
- Atc Item Name
- terbinafine
- Pharma Manufacturer Name
- GOLDPLUS UNIVERSAL PTE LTD
- Company Detail Path
- /organization/goldplus-universal-pte-ltd
