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POM-V Prescription Required Companion Animal

Dermipred 10 mg Tablets for Dogs

Active ingredient: Prednisolone

Form

Tablet

Species

Dogs

Manufacturer

Ceva Sante Animale

VMD MA No.

14966/3079

What it's used for

Streptococci (including S. uberis). Escherichia coli (including β-lactamase producing strains). AN: 01491/2024 & 01490/2024

Full indications, dosage and side effects ↓
View official SPC (PDF)

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Paying less for Prednisolone

  1. 1

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    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

Dermipred 10 mg Tablets for Dogs — SPC Details

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

Streptococci (including S. uberis).
Escherichia coli (including β-lactamase producing strains).
AN: 01491/2024 & 01490/2024
The dose and total duration of treatment is determined by the veterinarian per
individual case depending on the severity of symptoms. The lowest effective dose
must be used.
Starting dose:
- for dermatitis requiring an anti-inflammatory dose: 0.5 mg per kg bodyweight
twice a day.
- for dermatitis requiring an immunosuppressive dose: 1 - 3 mg per
kg bodyweight twice a day.
For longer term treatment: when after a period of daily dosing the desired effect
has been achieved, the dose should be reduced until the lowest effective dose is
reached. The reduction of the dose should be made by alternate day therapy and
/or by halving the dose with intervals of 5-7 days until the lowest effective dose is
reached.
For example, for a 10 kg dog requiring an anti-inflammatory dose of 0.5 mg/kg
twice a day, give one-half of a 10 mg-tablet twice a day.
AN: 02375/2025Page 5 of 7
Spontaneous intake by the animal or place the tablet behind the lingual torus.
Do not use in animals with:
- Viral, mycotic or parasitic infections that are not controlled with an
appropriate treatment
- Diabetes mellitus
- Hyperadrenocorticism
- Osteoporosis
- Heart failure
- Severe renal insufficiency
- Corneal ulceration
- Gastro-intestinal ulceration
- Glaucoma
Do not use concomitantly with attenuated live vaccines.
AN: 02375/2025Page 2 of 7
Do not use in known cases of hypersensitivity to the active substance, to other
corticosteroids, or to any of the excipients.
See also sections 3.7 and 3.8.
Dogs:
Very common
(>1 animal / 10 animals
treated):
Elevated triglyceride, hypocortisolaemia
Hypoadrenocorticism
Very rare
(<1 animal / 10,000
animals treated,
including isolated
reports):
Hyperadrenocorticism , Cushing’s disease ,
diabetes mellitus
Low thyroxine (T4), elevated liver enzymes, elevated serum alkaline
phosphatase (ALP), eosinopenia, lymphopenia, neutrophilia
Muscle wasting
Polyuria
Polydipsia
, polyphagia
Skin thinning
Gastrointestinal ulceration
, pancreatitis
Behavioural disorders,
Undetermined
frequency
(cannot be estimated
from the available data)
Elevated parathyroid (PTH) concentration, decreased lactate
dehydrogenase (LDH), decreased aspartate aminotransferase
(AST), hyperalbuminemia, hypernatraemia
, hypokalaemia
Muscle weakness, osteoporosis, inhibition of longitudinal growth of
bones
Increased weight, delayed healing, water retention, redistribution of
body fat
Opportunistic infection
Cutaneous calcinosis
is a consequence of the suppression of the hypothalamic-pituitary-adrenal axis.
Signs of adrenal insufficiency can arise following cessation of treatment, and this
may render the animal unable to deal adequately with stressful situations
particularly during the early stages of therapy
may be exacerbated by steroids in animals given non-steroidal anti-inflammatory
drugs and in animals with spinal cord trauma.
in case of long-term use.
the immunosuppressant action of corticosteroids may weaken resistance to
or exacerbate existing infections.
AN: 02375/2025Page 4 of 7
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or the national competent authority via the
national reporting system. See the package leaflet for respective contact details.
Glucocorticoids administration is to induce an improvement in clinical signs rather
than a cure. The treatment should be combined with treatment of the underlying
disease and/or environmental control.

Special precautions for safe use in the target species:
In cases where a bacterial infection is present the product should be used in
association with suitable antibacterial therapy. Pharmacologically-active dose
levels may result adrenal insufficiency. This may become apparent particularly after
withdrawal of corticosteroid treatment. This effect may be minimised by institution
of alternate-day therapy if practical. The dosage should be reduced and withdrawn
gradually to avoid precipitation of adrenal insufficiency (see section 3.9).
Corticoids such as prednisolone, exacerbate proteinaceous catabolism.
Consequently, the product should be carefully administered in old or malnourished
animals.
Corticoids such as prednisolone should be used with caution in patients with
hypertension, epilepsy, burns, previous steroid myopathy, in immunocompromised
animals and in young animals as corticosteroids may induce a delayed growth.
Treatment with the veterinary medicinal product may interfere with vaccination
efficacy. (See section 3.8)
Special monitoring is required in animals presenting with renal insufficiency. Use
only after careful benefit-risk assessment by the responsible veterinarian.
The tablets are flavoured. In order to avoid any accidental ingestion, store tablets out
of reach of the animals.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Prednisolone or other corticosteroids may cause hypersensitivity (allergic
reactions). People with known hypersensitivity to prednisolone or other
corticosteroids, or any of the excipients, should avoid contact with the veterinary
medicinal product.
To avoid accidental ingestion, particularly by a child, unused part-tablets should be
returned to the open blister space and inserted back into the carton. In case of
accidental ingestion, especially by a child, seek medical advice immediately and
show the package leaflet or the label to the physician.
Corticosteroids can cause foetal malformations; therefore it is recommended that
pregnant women avoid contact with the veterinary medicinal product. Immediately
wash hands thoroughly after handling the tablets.
AN: 02375/2025Page 3 of 7
Special precautions for the protection of the environment:
Not applicable.
Phenytoin, barbiturates, ephedrine and rifampicin may accelerate the metabolic
clearance of corticosteroids resulting in decreased blood levels and reduced
physiological effect.
The concomitant use of this veterinary medicinal product with non-steroidal anti-
inflammatory drugs may exacerbate gastrointestinal tract ulceration.
Administration of prednisolone may induce hypokalaemia and hence increase the
risk of toxicity from cardiac glycosides. The risk of hypokalaemia may be increased
if prednisolone is administered together with potassium depleting diuretics.
Precautions need to be taken when combining use with insulin.
When vaccinating with attenuated live vaccines, a two week interval should be
observed before or after treatment.
Do not store above 25°C.
Any unused tablet portion should be returned to the blister and be used for the next
administration.
Not applicable
4.

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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