Mycostatin

Country: Нови Зеланд

Језик: Енглески

Извор: Medsafe (Medicines Safety Authority)

Активни састојак:

Nystatin 25 mg/g equivalent to 100,000 U/g based on potency of 4400U/g, micropulverised, plus 10% overage.;  ; Nystatin 25 mg/g equivalent to 100,000 U/g based on potency of 4400 U/g, micropulverised, plus 10% overage.

Доступно од:

Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics

INN (Међународно име):

Nystatin 25 mg/g (=100,000 U/g based on potency of 4400U/g, micropulverised, plus 10% overage.)

Дозирање:

100000 U/mL

Фармацеутски облик:

Topical cream

Састав:

Active: Nystatin 25 mg/g equivalent to 100,000 U/g based on potency of 4400U/g, micropulverised, plus 10% overage.   Excipient: Aluminium hydroxide gel Perfume Promulgen D Propylene glycol Purified water Simeticone Sorbitol Titanium dioxide Water White soft paraffin Active: Nystatin 25 mg/g equivalent to 100,000 U/g based on potency of 4400 U/g, micropulverised, plus 10% overage. Excipient: Aluminium hydroxide gel Promulgen D Propylene glycol Purified water Simeticone Sorbitol Titanium dioxide Water White soft paraffin

Јединице у пакету:

Tube, 1 x 15 g, 15 g

Класа:

Pharmacy only

Тип рецептора:

Pharmacy only

Произведен од:

Patheon Capua SpA

Терапеутске индикације:

The treatment of candidal infections of the skin.

Резиме производа:

Package - Contents - Shelf Life: Tube, - 15 g - 24 months from date of manufacture stored at or below 25°C

Датум одобрења:

1972-05-05

Карактеристике производа

NEW ZEALAND DATA SHEET
1.
MYCOSTATIN (TOPICAL CREAM, 100000 U/ML)
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Mycostatin (Nystatin), 100,000 units/g: 15 g.
3.
PHARMACEUTICAL FORM
Topical cream 15g.
4.
CLINICALT PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Nystatin topical preparations are indicated in the treatment of
cutaneous or
mucocutaneous mycotic infections caused by Candida species.
This preparation is not indicated for systemic use.
4.2 DOSE AND METHOD OF ADMINISTRATION
Apply liberally to affected areas twice daily or as indicated until
healing is
complete.
4.3 CONTRAINDICATIONS
Known sensitivity to nystatin or other components.
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Should a reaction of hypersensitivity occur, the drug should be
immediately
withdrawn and appropriate measures taken. Nystatin topical
preparations
should not be used for the treatment of systemic or ophthalmic
infections.
It is recommended that KOH smears, cultures, or other diagnostic
methods
be used to confirm the diagnosis of cutaneous or mucocutaneous
candidiasis
and to rule out infection caused by other pathogens.
INFORMATION FOR THE PATIENT
Patients using these medications should receive the following
information and
instructions:
1. The patient should be instructed to use the medication as directed
(including the replacement of missed doses). The medication is not for
any disorder other than that for which it was prescribed.
2. Even if symptomatic relief occurs within the first few days of
treatment,
the patient should be advised not to interrupt or discontinue the
medication until the prescribed course of treatment is completed.
3. If symptoms of irritation develop, the patient should be advised to
notify
the physician promptly.
LABORATORY TEST
If there is a lack of therapeutic response, KOH smears, cultures or
other
diagnostic methods should be repeated.
CARCINOGENESIS AND MUTAGENESIS
No long-term animal studies have been performed to evaluate the
carcinogenic potential of nystatin.
4.5 INTERACTION WITH OTHER MEDICINES AND OTHER FO