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Vidalta

Active ingredient: Carbimazole

Sustained-release tablet for once-daily treatment of hyperthyroidism in cats. Pro-drug of thiamazole.

Form

Tablet

Strength

10mg to 15mg

Species

Cat

What it's used for

Treatment of hyperthyroidism and hyperthyroidism-associated clinical signs in cats. Revised: December 2024 AN: 02169/2024

Full indications, dosage and side effects ↓

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Paying less for Carbimazole

  1. 1

    Ask your vet for a written prescription

    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  2. 2

    Fill it at a registered online retailer

    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Vidalta — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

Treatment of hyperthyroidism and hyperthyroidism-associated clinical signs in cats.

Revised: December 2024
AN: 02169/2024
For oral use only.
Administration with food enhances bioavailability. The timing of treatment and its relation
to feeding should be kept consistent from day to day.
Do not break or crush the tablets as this will affect the sustained release property.
The aim of treatment is to maintain total thyroxine concentrations (TT4) in the lower end
of the reference range.
The following dose recommendations during the adjustment and maintenance phases
are suggested.
Dosing adjustment should primarily be based upon a clinical assessment of the individual
cat. Monitoring of TT4, full haematology and liver and kidney parameters is recommended
at each follow up visit (see sections 4.5 and 4.6).
Adjustment phase
The starting dose is a single daily oral administration of one tablet of 15 mg carbimazole
per cat. Consideration could be given to a starting dose of one 10 mg tablet daily where
the TT4 concentration is only mildly increased, e.g. between 50 nmol/L and 100 nmol/L.
With the recommended starting dose of one 15 mg tablet once daily, TT4 may decrease
to within the euthyroid range (TT4<50 nmol/L) shortly after treatment initiation. A dose
adjustment may be required as early as 10 days of treatment.
Dose adjustment should be also performed 3, 5 and 8 weeks after initiation of treatment,
depending on both clinical and hormonal responses to treatment.
Maintenance phase
Follow-up visits every 3 to 6 months are recommended. The dose should be adjusted
individually based on clinical signs and TT4. It is advisable to check TT4 10-14 days after
dose adjustment.
The therapeutic dose ranges between 10 mg (one 10 mg tablet) and 25 mg (one 10 mg
tablet and one 15 mg tablet) once daily.
Some cats require doses of less than 10 mg carbimazole daily. Every other day dosing
with 10 mg or 15 mg of carbimazole may be sufficient to control the disease.
Dose increases should not be made in increments of greater than 5 mg.
Doses above 20 mg have only been trialed in a small number of cats and should be used
with caution.

Revised: December 2024
AN: 02169/2024
Do not use in cats suffering from concurrent systemic diseases, such as severe primary
liver disease or diabetes mellitus.
Do not use in cats showing signs of auto-immune diseases and/or altered red or white
blood cell counts, such as anaemia, neutropaenia or lymphopaenia.
Do not use in cats with platelet disorders (particularly thrombocytopaenia) or
coagulopathies.
Do not use in cats with hypersensitivity to mercaptoimidazoles such as carbimazole or
thiamazole (methimazole) or to any of the excipients.
Please refer to section 4.7.
Treatment of hyperthyroidism may result in a reduction of renal perfusion. Azotaemia has
been reported in rare cases; depending on the severity, temporary or permanent
discontinuation of treatment may be required. Polydipsia and polyuria have also been
reported in rare (polydipsia) or very rare cases (polyuria).
Weight loss, vomiting, lethargy, tachycardia, reduced appetite, diarrhoea and dehydration
have been observed in rare cases.
Increased liver enzymes have been reported in rare cases. Severe cases may require
temporary or permanent discontinuation of treatment. However, these elevations are
usually reversible when treatment is discontinued, although symptomatic therapy
(nutritional and fluid support) may be required.
Anaemia, increase or decrease in white blood cell count, neutrophilia,
thrombocytopaenia, eosinophilia and/or lymphopaenia have been reported in rare cases,
in particular during the first 4-6 weeks of treatment. Discontinuation of treatment may be
required in case of persistent and marked disorder. In most cases, the abnormality will
resolve spontaneously within 1 month after the treatment has been discontinued.
Dermatological signs (pruritus, dermatitis, erythema, alopecia) have been reported in rare
cases. These clinical signs are usually mild, adequately controlled by symptomatic
therapy and do not require discontinuation of treatment. However, if more severe clinical

Revised: December 2024
AN: 02169/2024
signs occur that do not respond to symptomatic therapy, the dose should be reduced or
treatment stopped following a benefit-risk assessment by the responsible veterinarian.
Signs of gastrointestinal bleeding such as bloody vomit, oral haemorrhage or dark faeces
have been reported in rare cases.
Ataxia, pyrexia, dyspnoea, disorientation, aggressiveness, and positive antinuclear
antibody (ANA) have also been reported in very rare cases.
In cases of serious adverse reactions, mortality, possibly due to the product, might occur
if treatment is not discontinued. In many cases adverse reactions are reversible on
cessation of treatment.
The frequency of adverse reactions is defined using the following convention:




Thiamazole (methimazole), the active metabolite of carbimazole, inhibits thyroid hormone
production and therefore cessation of treatment with carbimazole will result in a rapid
(within 48 hours) return to pre-treatment thyroid hormone levels. Chronic administration
is therefore necessary unless surgical or radiation-induced thyroidectomy is performed.
A small proportion of cats with thyroid adenoma may fail to respond or have a poor
response to treatment.
Thyroid carcinoma is a rare cause of hyperthyroidism in the cat and medical management
alone is not recommended in such cases as it is not curative.

Special precautions for use in animals
Treatment should be adjusted according to a benefit-risk assessment by the responsible
veterinarian in each individual case.
Treatment of hyperthyroidism may result in a reduction in the glomerular filtration rate.
This can lead to unmasking of pre-existent renal dysfunction. Treatment of
hyperthyroidism may also induce an elevation of liver enzymes or a worsening of pre-
existing hepatic disorders. Renal and liver function should therefore be monitored before
and during treatment
Due to risk of leucopaenia or haemolytic anaemia, haematology parameters should be
monitored on a regular basis before and during treatment, preferably at each visit of the
dose adjustment phase and maintenance phase (see section 4.9).
Any animal that suddenly appears unwell during therapy, particularly if they are febrile,
should have a blood sample taken for routine haematology and biochemistry.
Neutropaenic animals (neutrophil counts <2.5 x 10
/L) should be treated prophylactically
with bactericidal antibiotics and supportive therapy.
Doses above 20 mg have only been trialled in a small number of cats and should be used
with caution.
Therefore, careful monitoring is recommended and the dose should be adjusted in
individual cases following a benefit-risk assessment by the responsible veterinarian.

Revised: December 2024
AN: 02169/2024
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
People with a known hypersensitivity (allergy) to carbimazole or any of the excipients
should avoid contact with the product.
If allergic symptoms develop, such as a skin rash, swelling of the face, lips or eyes or
difficulty in breathing, you should seek medical attention immediately and show the
package leaflet or label to the physician.
Carbimazole, as a prodrug of thiamazole (methimazole), may cause vomiting, epigastric
distress, headache, fever, arthralgia, pruritus and pancytopenia.
Avoid dermal contact and oral exposure, including hand-to-mouth contact.
Do not break or crush tablets.
Do not eat, drink or smoke while handling the tablet or used litter.
Wash hands with soap and water after administration of the product and when handling
litter used by treated animals.
In the case of accidental ingestion, seek medical advice immediately and show the
package or the label to the physician.
Carbimazole is a suspected human teratogen.
Women of child-bearing age must wear non-permeable, single use gloves when
administering the product or handling litter/vomit of treated cats. If you are
pregnant, think you may be pregnant or are attempting to conceive, you should not
administer the product or handle the litter/vomit of treated cats.
Concomitant treatment with phenobarbital may reduce the clinical efficacy of carbimazole.
Concomitant use of benzimidazole anthelmintics (fenbendazole or mebendazole) has
been shown to reduce the hepatic oxidation of this therapeutic class and may therefore
induce an increase in circulating levels. Accordingly, co-administration of carbimazole
with a benzimidazole is not recommended.
Thiamazole may display immunomodulating properties. This should be taken into account
when considering vaccination of the cat.

Revised: December 2024
AN: 02169/2024
Do not store above 25°C
Store in the original package.
Not applicable.
5.

This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.

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