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FUNGIFEX TABLET 250MG

Prescription Only
Drug type: Therapeutic
ATC code: D01BA02
Dosage form: TABLET
Route of administration: ORAL
Active ingredient: Terbinafine hydrochloride eqv Terbinafine

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

  • Known hypersensitivity to terbinafine or to any of the excipients of Fungifex.
  • Chronic or active hepatic disease.

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.

Registrant
GOLDPLUS UNIVERSAL PTE LTD
Approval Date
2024-01-05
Approval Number
SIN16925P
Manufacturer
Remedica Ltd
Licence Holder
GOLDPLUS UNIVERSAL PTE LTD
FUNGIFEX TABLET 250MG | MedPath