Sporanox 50mg/5ml oral solution

Страна: Велика Британія

мова: англійська

Джерело: MHRA (Medicines & Healthcare Products Regulatory Agency)

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Активний інгредієнт:

Itraconazole

Доступна з:

Janssen-Cilag Ltd

Код атс:

J02AC02

ІПН (Міжнародна Ім'я):

Itraconazole

Дозування:

10mg/1ml

Фармацевтична форма:

Oral solution

Адміністрація маршрут:

Oral

Клас:

No Controlled Drug Status

Тип рецепту:

Valid as a prescribable product

Огляд продуктів:

BNF: 05020100; GTIN: 5012674436066

інформаційний буклет

                                Page 1
PACKAGE LEAFLET: INFORMATION FOR THE USER SPORANOX 10 MG/ML ORAL SOLUTION
(itraconazole)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
•
Keep this leaflet. You may need to read it again.
•
If you have any further questions, ask your doctor or pharmacist.
•
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them even
if their symptoms are the same as yours.
•
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side effects
not listed in this leaflet.
WHAT IS IN THIS LEAFLET:
1.
WHAT SPORANOX ORAL SOLUTION IS AND WHAT IT IS USED FOR
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE SPORANOX ORAL SOLUTION
3.
HOW TO USE SPORANOX ORAL SOLUTION
4.
POSSIBLE SIDE EFFECTS
5.
HOW TO STORE SPORANOX ORAL SOLUTION
6.
CONTENTS OF THE PACK AND OTHER INFORMATION
1.
WHAT SPORANOX ORAL SOLUTION IS AND WHAT IT IS USED FOR
Sporanox is one of a group of medicines called “antifungals”.
These medicines are used to treat and stop
you from getting infections caused by fungi including yeasts.
You may be given Sporanox to
:
•
treat yeast infections of the mouth, throat or gullet if you have a
poor immune system
•
stop you from getting certain fungal infections if you have a poor
immune system due to a major
blood disorder or bone marrow transplantation.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE SPORANOX ORAL SOLUTION
DO NOT USE SPORANOX ORAL SOLUTION IF YOU ARE:
•
ALLERGIC
(hypersensitive) to itraconazole or to any of the ingredients in
Sporanox oral solution (listed
in Section 6
Contents of the pack and other information)
•
PREGNANT
, think you might be pregnant or could become pregnant (see the
section on Pregnancy)
•
TAKING ANY OF THE FOLLOWING MEDICINES:
o
terfenadine or mizolastine (antihistamines for allergies)
o
bepridil, ivabradine or ranolazine - used to treat angina (crushing
chest pain)
o
nisoldipine, lercanidipine or eplerenone (used for high blood
pressure)

                                
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Характеристики продукта

                                OBJECT 1
SPORANOX 10 MG/ML ORAL SOLUTION
Summary of Product Characteristics Updated 01-Mar-2018 | Janssen-Cilag
Ltd
1. Name of the medicinal product
SPORANOX 10 mg/ml Oral Solution.
2. Qualitative and quantitative composition
1 ml SPORANOX Oral Solution contains 10 mg itraconazole.
Sorbitol E420 (190 microlitre per ml).
For a full list of excipients, see section 6.1.
3. Pharmaceutical form
Oral solution.
SPORANOX Oral Solution is clear, yellow to slightly amber solution
with an odour of cherry.
4. Clinical particulars
4.1 Therapeutic indications
SPORANOX Oral Solution is indicated:
- for the treatment of oral and/or oesophageal candidosis in
HIV-positive or other immunocompromised
patients.
- as prophylaxis of deep fungal infections anticipated to be
susceptible to itraconazole, when standard
therapy is considered inappropriate, in patients with haematological
malignancy or undergoing bone
marrow transplant, and who are expected to become neutropenic (i.e. <
500 cells/µl). At present, there are
insufficient clinical efficacy data in the prevention of
aspergillosis.
Consideration should be given to national and/or local guidance
regarding the appropriate use of
antifungal agents.
4.2 Posology and method of administration
For optimal absorption, SPORANOX Oral Solution should be taken without
food (patients are advised to
refrain from eating for at least 1 hour after intake).
For the treatment of oral and/or oesophageal candidosis, the liquid
should be swished around the oral
cavity (approx. 20 seconds) and swallowed. There should be no rinsing
after swallowing.
- Treatment of oral and/or oesophageal candidosis: 200 mg (2 measuring
cups) per day in two intakes, or
alternatively in one intake, for 1 week. If there is no response after
1 week, treatment should be continued
for another week.
- Treatment of fluconazole resistant oral and/or oesophageal
candidosis: 100 to 200 mg (1-2 measuring
cups) twice daily for 2 weeks. If there is no response after 2 weeks,
treatment should be continued for
another 2 weeks. The 400
                                
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