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Canesten

Canesten

About the medicine

How to use Canesten

Leaflet attached to the packaging: patient information

Canesten, 500 mg, vaginal tablet

Clotrimazole

Please read carefully the contents of the leaflet before using the medicine, as it contains important information for the patient.

This medicine should always be used exactly as described in the patient leaflet or as directed by a doctor or pharmacist.

  • This leaflet should be kept in case it needs to be read again.
  • If advice or additional information is needed, a pharmacist should be consulted.
  • If the patient experiences any side effects, including any not listed in this leaflet, they should inform their doctor or pharmacist. See section 4.
  • If there is no improvement after 7 days or the patient feels worse, they should contact their doctor.

Table of contents of the leaflet

  • 1. What is Canesten and what is it used for
  • 2. Important information before using Canesten
  • 3. How to use Canesten
  • 4. Possible side effects
  • 5. How to store Canesten
  • 6. Contents of the packaging and other information

1. What is Canesten and what is it used for

The active substance of Canesten is clotrimazole, which belongs to a group of medicines called imidazoles. It has a broad spectrum of antifungal activity, meaning it destroys fungi and inhibits their growth. It is effective against microorganisms such as dermatophytes, yeasts, and molds. Canesten is used to treat vaginal and external genital infectionscaused by microorganisms such as fungi (usually Candida), which are sensitive to clotrimazole.Symptoms include itching, burning, discharge (thick, white to yellow, odorless vaginal discharge similar to cottage cheese), redness, swelling, and pain. Only a doctor can make a reliable diagnosis of a fungal infection and determine the sensitivity of the microorganism to clotrimazole. The information in section 2 of the leaflet should be read to determine when to consult a doctor before using Canesten. The medicine is intended for use in adults and adolescents from 16 years of age.

2. Important information before using Canesten

When not to use Canesten:

  • if the patient is allergicto clotrimazole or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Before starting to use Canesten, the patient should discuss it with their doctor:

  • if the vaginal infection occurs for the first time,
  • if the vaginal infection occurs during the first trimester of pregnancy,
  • in case of recurrent infections, if there have been at least 2 cases of infection in the last 6 months,
  • in case of a fever of 38°C or higher,
  • if the patient experiences lower abdominal pain, back pain,
  • in case of foul-smelling discharge,
  • if the patient experiences nausea,
  • if there is vaginal bleeding and (or) arm pain.

Canesten should not be used during menstruation. The use of this medicine should be stopped before the start of menstrual bleeding. During the use of Canesten, tampons, douching, spermicides, or other vaginal products should not be used. During the use of Canesten and during the vaginal infection, sexual intercourse should be avoided, as the infection can be transmitted to the sexual partner. The sexual partner should also be treated locally if they have symptoms of a yeast infection. Treating sexual partners can help prevent reinfection. The contraceptive effectiveness of latex contraceptives, such as condoms and diaphragms, may be reduced. Canesten should not be swallowed.

Children and adolescents

Canesten should not be used in girls under 16 years of age without consulting a doctor.

Canesten and other medicines

The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take. The patient should inform their doctor if they are taking tacrolimusor sirolimus, medicines used to control the immune response after organ transplantation. It is possible that the concentration of some medicines in the patient's blood may increase if they are used at the same time as Canesten. However, this is unlikely in the case of a single 500 mg dose. If there are any doubts about using another medicine with Canesten, the patient should consult their doctor.

Pregnancy and breastfeeding

If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.

Pregnancy

Before using clotrimazole during the first 3 months of pregnancy, the patient should consult their doctor. If Canesten is used during pregnancy, the applicator included in the packaging should not be used. The tablet should be inserted into the vagina with the finger to avoid injuring the cervix.

Breastfeeding

Canesten can be used during breastfeeding. If there are any doubts, the patient should consult their doctor or pharmacist.

Driving and using machines

Canesten does not affect the ability to drive or use machines.

3. How to use Canesten

This medicine should always be used exactly as described in the patient leaflet or as directed by a doctor or pharmacist. If there are any doubts, the patient should consult their doctor or pharmacist. The recommended dose is for adults and adolescents from 16 years of age

  • one vaginal tablet, inserted deeply into the vagina, in a single dose, in the evening.

The vaginal environment should be kept moist to allow the tablet to dissolve completely. Otherwise, undissolved parts of the tablet may slip out of the vagina. The treatment may be repeated. However, recurrent infections may indicate another disease causing the symptoms. If the symptoms recur, the patient should consult their doctor.

Instructions for use

The vaginal tablet should be inserted into the vagina as deeply as possible, using the applicator included with the medicine, preferably in a lying position, in the evening before sleep. The hands should be washed before removing the vaginal tablet and applicator from the packaging and again after using the applicator.

  • 1. Remove the applicator from the packaging and pull out the plunger and red lock.
  • 2. Place the vaginal tablet in the applicator, with the curved part inside the applicator. Press the plunger and lock into the applicator until a click is felt.
  • 3. After feeling the click, remove the lock from the plunger and carefully insert the applicator into the vagina until the textured area on the handle is reached.
Applicator with body, plunger, and red lock, vaginal tablet next to it with labelsTwo hands holding the applicator, vaginal tablet being inserted into the applicator, arrow indicating the direction of insertionHand holding the applicator with the tablet, red lock visible next to the applicator
  • 4. Hold the applicator at the textured area on the handle and carefully press the plunger to the end, until it stops, to apply the vaginal tablet.
Hands inserting the applicator into the vagina, applicator between the legs

After use, the applicator should be disposed of in a safe place, out of the reach of children. The applicator should not be flushed down the toilet. The method of using vaginal tablets without an applicator is as follows: If the patient is pregnant, the vaginal tablet should be inserted into the vagina with the finger.

Duration of treatment

Canesten is used for the treatment in a single dose. If there is no significant improvement after 7 daysof use, the patient should consult their doctorto confirm the cause of the infection. If the symptoms worsen, the patient should contact their doctor.

Use in children and adolescents

Canesten should not be used in girls under 16 years of age without consulting a doctor. If there are any further doubts about using this medicine, the patient should consult their doctor.

4. Possible side effects

Like all medicines, Canesten can cause side effects, although not everybody gets them. Side effects have been observed with the following frequency:

Common, more than 1 in 100 people:

  • burning

Uncommon, more than 1 in 1000 people:

  • abdominal pain
  • itching
  • redness of the skin and (or) irritation

Rare, more than 1 in 10,000 people:

  • allergic reactions
  • swelling
  • skin rash
  • vaginal bleeding

Frequency not known, based on available data:

  • vaginal shedding
  • feeling of discomfort in the vagina
  • vaginal pain
  • nausea
  • hives
  • discharge
  • pain

The use of Canesten should be stopped if the patient experiences local side effects or allergic reactions (including anaphylactic reaction, angioedema, low blood pressure, shortness of breath, and (or) fainting). Local side effects may be similar to the symptoms of the disease, making it difficult to distinguish between the symptoms of the infection and the side effects caused by the medicine.

Reporting side effects

If any side effects occur, including any not listed in the leaflet, the patient should inform their doctor or pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: 22 49-21-301, fax: 22 49-21-309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, more information can be collected on the safety of the medicine.

5. How to store Canesten

The medicine should be stored in a place that is out of sight and reach of children. It should not be stored at a temperature above 25°C. The medicine should not be used after the expiry date stated on the packaging and blister after: EXP. The expiry date refers to the last day of the specified month. Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.

6. Contents of the packaging and other information

What Canesten contains

  • The active substance of Canesten is clotrimazole.
  • The other ingredients (excipients) are: calcium lactate pentahydrate; microcrystalline cellulose; hypromellose 15cP; lactic acid; lactose monohydrate; corn starch; magnesium stearate; colloidal silica, anhydrous; crospovidone.

What Canesten looks like and contents of the packaging

White vaginal tablet with markings MU and Bayer. One vaginal tablet, in a blister and applicator, in a cardboard box.

Marketing authorization holder

Bayer Sp. z o.o. Al. Jerozolimskie 158, 02-326 Warsaw, tel. +48 22 5723500

Manufacturer

GP Grenzach Produktions GmbH, Emil-Barell-Strasse 7, 79639 Grenzach-Wyhlen, Germany

This medicinal product is authorized for sale in the Member States of the European Economic Area under the following names:

Finland: Canesten, 500 mg vaginal tablet, Poland: Canesten, 500 mg, vaginal tablet, Date of last revision of the leaflet:05.2022

  • Country of registration
  • Active substance
  • Prescription required
    No
  • Manufacturer
  • Importer
    GP Grenzach Produktions GmbH

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