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Bayer plc

Bayer House, Strawberry Hill, Newbury, Berkshire, RG14 1JA
Telephone: +44 (0)1635 563 000
Fax: +44 (0)1635 563 393
WWW: http://www.bayer.co.uk

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Summary of Product Characteristics last updated on the eMC: 20/09/2010
SPC Canesten 200mg Pessary


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1. NAME OF THE MEDICINAL PRODUCT

Canesten 200mg Pessary.


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2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Clotrimazole 200mg

For excipients, see 6.1


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3. PHARMACEUTICAL FORM

Pessary


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4. CLINICAL PARTICULARS

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4.1 Therapeutic indications

Canesten 200mg Pessaries are recommended for the treatment of candidal vaginitis.


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4.2 Posology and method of administration

The pessaries should be inserted into the vagina, as high as possible, using the applicator provided. This is best achieved when lying back with legs bent up.

Adults:

One pessary should be inserted daily (preferably at night) for three consecutive days. A second treatment may be carried out if necessary.

There is no separate dosage schedule for the elderly.

Canesten pessaries need moisture in the vagina in order to dissolve completely, otherwise undissolved pieces of the pessary might crumble out of the vagina. Pieces of undissolved pessary may be noticed by women who experience vaginal dryness. To help prevent this it is important that the pessary is inserted as high as possible in to the vagina at bedtime.

Generally:

treatment during the menstrual period should not be performed due to the risk of the pessary being washed out by the menstrual flow. The treatment should be finished before the onset of menstruation.

Do not use tampons, intravaginal douches, spermicides or other vaginal products while using this product.

Children:

Not for use in children under 16.


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4.3 Contraindications

Hypersensitivity to clotrimazole or any of the excipients in this product.


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4.4 Special warnings and precautions for use

Medical advice should be sought if this is the first time the patient has experienced symptoms of candidal vaginitis.

Before using Canesten 200mg Pessaries, medical advice must be sought if any of the following are applicable:

- more than two infections of candidal vaginitis in the last six months.

- previous history of a sexually transmitted disease or exposure to partner with sexually transmitted disease.

- pregnancy or suspected pregnancy.

- aged under 16 or over 60 years.

- known hypersensitivity to imidazoles or other vaginal anti-fungal products.

Canesten 200mg Pessaries should not be used if the patient has any of the following symptoms whereupon medical advice should be sought:

- irregular vaginal bleeding.

- abnormal vaginal bleeding or a blood-stained discharge.

- vulval or vaginal ulcers, blisters or sores.

- lower abdominal pain or dysuria.

- any adverse events such as redness, irritation or swelling associated with the treatment.

- fever or chills.

- nausea or vomiting.

- diarrhoea.

- foul smelling vaginal discharge.

Patients should be advised to consult their physician if the symptoms have not been relieved within one week of using Canesten 200mg Pessaries. The pessaries can be used again if the candidal infection returns after 7 days. However, if the candidal infection recurs more than twice within six months, patients should be advised to consult their physician.


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4.5 Interaction with other medicinal products and other forms of interaction

Laboratory tests have suggested that, when used together, this product may cause damage to latex contraceptives. Consequently, the effectiveness of such contraceptives may be reduced. Patients should be advised to use alternative precautions for at least five days after using this product.

Concomitant medication with vaginal clotrimazole and oral tacrolimus (FK-506; immunosuppressant) might lead to increased tacrolimus plasma levels. Patients should thus be closely monitored for signs and symptoms of tacrolimus overdosage, if necessary by determination of the respective plasma levels.


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4.6 Pregnancy and lactation

Data on a large number of exposed pregnancies indicate no adverse effects of Clotrimazole on pregnancy or on the health of the foetus/newborn child. To date, no relevant epidemiological data are available.

Clotrimazole can be used during pregnancy, but only under the supervision of a physician or midwife.

During pregnancy the pessary should be inserted without using an applicator.


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4.7 Effects on ability to drive and use machines

Not applicable.


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4.8 Undesirable effects

As the listed undesirable effects are based on spontaneous reports, assigning accurate frequency of occurrence for each is not possible.

Immune system disorders:

allergic reaction (syncope, hypotension, dyspnea, urticaria, pruritus)

Reproductive system and breast disorders:

genital peeling, pruritus, rash, oedema, discomfort, burning, irritation, pelvic pain

Gastrointestinal disorders:

abdominal pain


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4.9 Overdose

In the event of accidental oral ingestion, routine measures such as gastric lavage should be performed only if clinical symptoms of overdose become apparent (e.g. dizziness, nausea or vomiting). It should be carried out only if the airway can be protected adequately.


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5. PHARMACOLOGICAL PROPERTIES

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5.1 Pharmacodynamic properties

ATC Code: G01A F02

Clotrimazole is an imidazole derivative with a broad spectrum of antimycotic activity.

Mechanism of Action

Clotrimazole acts against fungi by inhibiting ergosterol synthesis. Inhibition of ergosterol synthesis leads to structural and functional impairment of the cytoplasmic membrane.

Pharmacodynamic Effects

Clotrimazole has a broad antimycotic spectrum of action in vitro and in vivo, which includes dermatophytes, yeasts, moulds, etc.

The mode of action of clotrimazole is fungistatic or fungicidal depending on the concentration of clotrimazole at the site of infection. In-vitro activity is limited to proliferating fungal elements; fungal spores are only slightly sensitive.

Primarily resistant variants of sensitive fungal species are very rare; the development of secondary resistance by sensitive fungi has so far only been observed in very isolated cases under therapeutic conditions.


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5.2 Pharmacokinetic properties

Pharmacokinetic investigations after vaginal application have shown that only a small amount of clotrimazole (3 – 10% of the dose) is absorbed. Due to the rapid hepatic metabolism of absorbed clotrimazole into pharmacologically inactive metabolites the resulting peak plasma concentrations of clotrimazole after vaginal application of a 500mg dose were less than 10 ng/ml, reflecting that clotrimazole applied intravaginally does not lead to measurable systemic effects or side effects.


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5.3 Preclinical safety data

There are no pre-clinical data of relevance to the prescriber which are additional to the information included in other sections of the SPC.


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6. PHARMACEUTICAL PARTICULARS

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6.1 List of excipients

Calcium lactate pentahydrate

Maize starch

Crospovidone

Silica, colloidal anhydrous

Lactic acid

Lactose Monohydrate

Magnesium Stearate

Hypromellose

Cellulose, microcrystalline


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6.2 Incompatibilities

Not applicable.


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6.3 Shelf life

48 months.


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6.4 Special precautions for storage

No special precautions for storage


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6.5 Nature and contents of container

Three pessaries are packed in a blister pack (foil 25µm PA + 45µm Al soft + 60µm PVC) sealed with aluminium backing foil (foil 20µm Al hard + 7g/m2 HSL sealable to PVC/PVDC). An applicator is also provided.

The pessaries and applicator are enclosed in a cardboard carton.


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6.6 Special precautions for disposal and other handling

1. Pull out plunger A until it stops.

Place pessary into the applicator.

2. Insert applicator containing the pessary carefully as deeply as is comfortable into the vagina. (This is best done with the patient lying on her back with the knees bent up.)

3. Push plunger A until it stops, thereby depositing the pessary into the vagina. Remove the applicator.

4. After use, remove plunger A completely by pulling it out of the applicator B.

Then wash it in warm (not boiling) soapy water, rinse and dry carefully.

 

 


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7. MARKETING AUTHORISATION HOLDER

Bayer plc

Bayer House

Strawberry Hill

Newbury, Berkshire

RG14 1JA

Trading as Bayer plc, Consumer Care Division


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8. MARKETING AUTHORISATION NUMBER(S)

PL 0010/0072


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9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

Date of first authorisation: 21 September 1979

Date of last renewal of authorisation: 10 November 1999


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10. DATE OF REVISION OF THE TEXT

12/08/2010


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LEGAL CATEGORY

P



More information about this product

Link to this document from your website: http://www.medicines.org.uk/emc/medicine/4017/SPC/


Active Ingredients/Generics

 
   clotrimazole