Label: information for the user
Gine-Canestén 20 mg/g vaginal cream
clotrimazol
Read this label carefully before starting to use this medication, as it contains important information for you.
Follow exactly the administration instructions contained in this label or those indicated by your doctor, pharmacist, or nurse.
Contents of the package and additional information
Clotrimazole is an antifungal (a medicine used to treat infections caused by fungi).
This medicine is indicated for the treatment of uncomplicated vulvovaginal candidiasis (vaginal infection caused by a fungus called Candida) (See Warnings and Precautions section).
The main symptoms are itching, usually accompanied by an increase in vaginal discharge, pain, and redness of the vaginal and vulvar areas, burning, and a sensation of scalding when urinating. These symptoms are not specific to vulvovaginal candidiasis. If in doubt, consult your doctor.
No use Gine-Canestén
Warnings and Precautions
Consult your doctor, pharmacist or nurse before starting to use Gine-Canestén.
Do not ingest.
Inform your doctor if you have problems with your immune system, for example if you are being treated with oral corticosteroids or have HIV, AIDS or diabetes.
You must consult a doctor if symptoms worsen during treatment or persist after 3 days or if you observe an increase in vaginal discharge or changes in its appearance or odor, or if you experience vaginal bleeding.
In case of fever (38°C or higher), abdominal or back pain, lower back pain, abundant watery vaginal secretions and/or nausea, you must consult your doctor to rule out another type of disease.
Avoid contact with the eyes, as it would cause irritation. If accidental contact with the eyes occurs, wash with abundant water and consult an ophthalmologist if necessary.
Do not use tampons, vaginal douches, spermicides or other vaginal products while using this medication.
Do not start treatment during menstruation..Treatment must have ended before the start of menstruation.
In case of an allergic reaction during its use, treatment must be suspended and you must immediately consult your doctor. Signs of a severe allergic reaction include swollen and itchy rash, swelling, sometimes on the face or in the mouth that causes difficulty breathing.
This medication may reduce the effectiveness and safety of latex products, such as condoms and diaphragms. This effect is temporary and only appears during treatment.
It is recommended to avoid sexual intercourse in case of vaginal infection and while using this medication to prevent the partner from becoming infected.
Use in Children
Do not use in children under 12 years old.
Use of Gine-Canestén with Other Medications
Inform your doctor or pharmacist that you are taking, have recently taken or may need to take any other medication, especially if you are taking tacrolimus or sirolimus (medications used in transplant patients)
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant or intend to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
Clotrimazol can be used during pregnancy, but only under the supervision of a healthcare professional.
In case of treatment during the last 4 or 6 weeks of pregnancy, the use of the applicator is not recommended. Therefore, the use of vaginal tablets instead of vaginal cream is recommended, as these can be inserted directly with the finger, after careful washing of the hands.
Breastfeeding
Clotrimazol can be used during breastfeeding.
Driving and Operating Machines
The influence of Gine-Canestén on the ability to drive and operate machines is negligible or insignificant.
Gine-Canestén contains alcohol cetoestearílico and alcohol bencílico
This medication may cause local reactions on the skin (such as contact dermatitis) because it contains alcohol cetoestearílico.
This medication contains 20 mg of alcohol bencílico in each gram of cream.
Alcohol bencílico may cause allergic reactions.
Alcohol bencílico may cause moderate local irritation.
Follow exactly the administration instructions of this medication contained in this leaflet or those indicated by your doctor, pharmacist, or nurse. In case of doubt, ask your doctor, pharmacist, or nurse.
The recommended dose is:
Adults and adolescents over 12 years old
This medication is administered via the vagina.
Generally, it is sufficient to apply a charge of the vaginal applicator (5 g approx.), once a day, preferably at night before going to bed, for 3 consecutive days. The cream must be introduced deeply into the vagina (see applicator instructions), with the patient lying on their back and with their legs slightly bent.
If symptoms persist after completing treatment or recur within two months or if you have problems with your immune system, HIV infection, AIDS, or diabetes, you must consult with your doctor.
Use in children
Do not use in children under 12 years old.
If you use more Gine-Canestén than you should
An accidental ingestion may cause gastrointestinal discomfort and/or vomiting. An accidental administration in the eyes may cause burning and eye irritation without severity.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service. Phone (91) 562 04 20 indicating the medication and the amount ingested.
If you forgot to use Gine-Canestén
In case of forgotten dose, wait for the next one. Do not apply a double dose to compensate for the missed dose.
If you interrupt the treatment with Gine-Canestén
Continue using Gine-Canestén until you complete the treatment, even if you feel better. You need to use the complete treatment to cure the infection. If you interrupt the treatment, the fungi may not have disappeared.
If you have any other questions about the use of this medication, ask your doctor.
Like all medications, Gine-Canestén may produce adverse effects, although not everyone will experience them.
Adverse reactions withunknown frequency (cannot be estimated from available data)are:
Immune System Disorders:
Angioedema (swelling under the skin), allergic reaction, hypersensitivity.
Vascular Disorders:
Syncope (sudden loss of consciousness, fainting), hypotension (low blood pressure).
Respiratory, Thoracic, and Mediastinal Disorders:
Difficulty breathing.
Gastrointestinal Disorders:
Abdominal pain, nausea.
Skin and Subcutaneous Tissue Disorders:
Rash, urticaria (raised, red, itchy patches).
Reproductive and Mammary System Disorders:
Vaginal desquamation, vaginal discharge, vulvovaginal itching, vulvovaginal erythema, sensation of burning in the genital area, vulvovaginal discomfort, vulvovaginal pain, and vaginal bleeding.
General and Localized Disorders:
Irritation at the application site, edema, pain.
These symptoms usually do not require discontinuation of treatment and are more frequent during the first days of treatment.
Reporting Adverse Effects:
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use: http;//www.notificaram.es. By reporting adverse effects, you can contribute to providing more information about the safety of this medication
No requires special conditions for conservation.
Keep this medication out of the sight and reach of children.
Do not use Gine-Canestén after the expiration date that appears on the packaging, afterthe abbreviation CAD. Theexpiration date is the last day of the month indicated.
Medicines should not be thrown down the drain or inthe trash. Disposeof the packaging and the medication that you do not need at thePharmaceutical Take-Backpoint ofthe pharmacy. Incase of doubt, ask your pharmacist how to dispose of the packaging and the medication that you do not need. In this way, you will help to protect the environment.
Composition of Gine-Canestén
Appearance of the product and contents of the packaging:
This medication is a white cream. It is presented in a cardboard box containing an aluminum tube with a plastic stopper, containing 20 g of cream, and 3 disposable plastic vaginal applicators.
Holder of the marketing authorization
BAYER HISPANIA, S.L.
Av. Baix Llobregat, 3 – 5
08970 Sant Joan Despí (Barcelona)
Spain
Responsible for manufacturing
GP Grenzach Produktions GmbH
Emil-Barell-Str. 7
79639 Grenzach-Wyhlen
Germany
Last review date of this leaflet: February 2022
The detailed and updated information on this medication is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS)atthe following link:http://www.aemps.gob.es/
INSTRUCTIONS FOR USE OF THE APPLICATOR 1.Remove the stopper from the tube and attach the applicator. 2.Fill the applicator by carefully pressing the tube until the plunger reaches the top. 3.Separate the applicator from the tube and insert it as deeply as possible into the vagina (preferably with the patient lying on her back and with her legs slightly bent), emptying it by pressing the plunger. 4.Remove the applicator and discard it. |
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