Product Ref: APKEL06 Category: K
Kelactin is an oral dog and cat medication used to treat false pregnancy in bitches and suppression of lactation in bitches and queens. It contains the active substance cabergoline which is a pale yellow, viscous oily solution that inhibits processes such as lactation.
Kelactin works by binding to dopamine receptors in the pituitary gland, which prevents the release of prolactin. This reduces milk production and helps to dry up milk secretion. It also suppresses false pregnancy symptoms such as nesting behaviour and mammary gland development in bitches.
How To Buy Kelactin For Cats & Dogs
Kelactin for dogs and cats is a non-prescription medication that can be bought from our online store. This product must be kept refrigerated and so express delivery is required. Buying your cat and dog medication online is a simple process that means you can buy kelactin online instead of going to your vet every month.
How To Use Kelactin For Cats & Dogs
The veterinary medicinal product should be administered orally either directly into the mouth or by mixing with food. The dosage is 0.1 ml/kg bodyweight (equivalent to 5 microgram/kg bodyweight of cabergoline) once daily for 4-6 consecutive days, depending on the severity of the clinical condition. The weight of the treated animal should be accurately determined before administration.
Target species
Dog and cat.
4.2 Indications for use, specifying the target species
The veterinary medicinal product is indicated for the following uses:
4.3 Contra-indications
Do not use in pregnant animals since the product may cause abortion. Do not use with dopamine antagonist. Do not use in case of hypersensitivity to the active substance or to any of the excipients.
Cabergoline may induce transient hypotension in treated animals. Do not use in animals concurrently being treated with hypotensive drugs. Do not use directly after surgery whilst the animal is still under the influence of the anaesthetic agents.
4.4 Special warnings for each target species
Additional supportive treatments should involve restriction of water and carbohydrate intake and increase exercise.
4.5 Special precautions for use
i) Special precautions for use in animals
Not applicable.
(ii) Special precautions to be taken by the person administering the veterinary medicinal product to animals
Wash hand after use. Avoid contact with skin and eyes. Wash of any splashes immediately. Women of childbearing potential and breast-feeding woman should not handle the product or should wear disposable gloves when administering the product. People with known hypersensitivity to cabergoline or any of the other ingredients in the product should avoid contact with the veterinary medicinal product. Do not leave unattended filled syringes in presence of children. In the event of accidental ingestion, particularly by a child, seek medical attention immediately and show the package leaflet or the label to the physician.
4.6 Adverse reactions (frequency and seriousness)
Possible adverse effects are:
These adverse effects are usually of a moderate and transient nature. Vomiting usually only occurs after the first administration. In this case treatment should not be stopped, since the vomiting will not reoccur after the following administrations. In very rare cases allergic reactions may occur, such as oedema, urticaria, dermatitis and pruritus. In very rare cases a transient hypotension may occur. In very rare cases neurological symptoms may occur, such as sleepiness, muscle tremor, ataxia, hyperactivity and convulsions.
The frequency of adverse reactions is defined using the following convention:
4.7 Use during pregnancy, lactation or lay
Cabergoline has the capacity to cause abortion in the later stages of pregnancy and should not be used in pregnant animals. Differential diagnosis between pregnancy and false pregnancy should be made correctly. The product is indicated for the suppression of lactation: inhibition of prolactin secretion by cabergoline results in a rapid cessation of lactation and a reduction in the size of the mammary glands. The product should not be used in lactating animals unless suppression of lactation is required.
4.8 Interaction with other medicinal products and other forms of interaction
Since cabergoline exerts its therapeutic effect by direct stimulation of dopamine receptors, the product should not be administered concurrently with drugs which have dopamine antagonist activity (such as phenothiazines, butyrophenones, metoclopramide), as these might reduce its prolactin inhibiting effects.
Since cabergoline may induce transient hypotension, the product should not be used in animals concurrently treated with hypotensive drugs.
Royal Mail 2nd Class / Parcel Force 48
UK to UK :Normally arrives in 2-4 business days.
UK to Ireland :Normally arrives in 4-6 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note standered delivery is none trackable , none insured , no responsabily for lose or Damage
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Royal Mail First Class / Parcel Force 24
UK to UK :Normally arrives in 1-2 business days.
UK to Ireland 3-4 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note :Trackable , Royal Mail insured up to £50.
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Parcel Force Express AM Guaranteed before Midday.
UK to UK only . UP to 5KG Max Weight
Arrives next day before 12 noon, requires a signature.
Parcel Forcel Terms & Conditions apply
Important: Parcel Force advise that there are some postcodes where an extended delivery time exists, and may affect the date of delivery or the service is not available.
Category | POM-V |
Temperature | Refrigerated |
MA/VM/EU No: | 27569/4008 |
Species |
|
VMD Link | Product Information Database (defra.gov.uk) |
NOAH Link | |
Dosage | The veterinary medicinal product should be administered orally either directly into the mouth or by mixing with food. The dosage is 0.1 ml/kg bodyweight (equivalent to 5 microgram/kg bodyweight of cabergoline) once daily for 4-6 consecutive days, depending on the severity of the clinical condition. If the signs fail to resolve after a single course of treatment, or if they recur after the end of treatment, then the course of treatment may be repeated. The weight of treated animal should be accurately determined before administration. How to withdraw the recommended volume from the vial ? a. Remove the cover from the vial adapter package. Do not remove the vial adapter from the blister package. b. Attach the adapter to the vial; use the blister pack to handle the adapter. Seat the adapter on the vial by pushing down until the spike penetrates the stopper and the adapter snaps in place. c. Remove and discard the blister package. d. Attach the syringe to the adapter by firmly pressing the syringe into the vial adapter to avoid leaking of the product when withdrawing the dose from the vial. e. Withdraw the drug from the vial into the syringe holding the vial upside down. f. Remove the syringe from the adapter. g. The drug is now ready for administration. It is recommended to rinse and dry the syringe following each application. a. b. c. d. e. f. g. 4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary The experimental data indicate that a single overdose with cabergoline might result in an increased likelihood of post-treatment vomiting, and possibly an increase in post-treatment hypotension. General supportive measures should be undertaken to remove any unabsorbed drug and maintain blood pressure, if necessary. As an antidote, the parental administration of dopamine antagonist drugs such as metoclopramide might be considered. |
Withdrawals | Not applicable. |