Carprogesic 100 Mg Tablets For Dogs

Revised: August 2014

AN. 00392/2013


1. Name of the Veterinary Medicinal Product

Carprogesic 100 mg Tablets for Dogs. (UK, AT, BE, DE, EL, FR, IE, LU, NL, PT, ES)

Profenacarp 100 mg Tablets for Dogs. (IT)

2. Qualitative and Quantitative Composition

Each tablet contains:

Active Ingredient:

Carprofen 100 mg


Tartrazine (E102) 1.2 mg

For the full list of excipients, see Section 6.1

3. Pharmaceutical Form


A yellow circular tablet of 8 mm diameter, embossed “100” on one side and a single breakline on the other side.

The tablets can be divided into halves.

4. Clinical Particulars

4.1 Target Species:


4.2 Indications for Use, Specifying the Target Species:

In the dog:

Reduction of inflammation and pain caused by musculoskeletal disorders and degenerative joint disease. As a follow up to parenteral analgesia in the management of post operative pain.

4.3 Contraindications:

Do not use in cats.

Do not use in pregnant or lactating bitches.

Do not use in puppies less than 4 months of age.

Do not use in animals with known hypersensitivity to the active substance or to any of the excipients

Do not use in dogs suffering from cardiac, hepatic or renal disease, where there is a possibility of gastrointestinal ulceration or bleeding, or where there is evidence of a blood dyscrasia.

4.4 Special Warnings for Each Target Species:

Refer to Sections 4.3 and 4.5.

4.5 Special Precautions for Use:

Special precautions for use in animals

Use in aged dogs may involve additional risk.

If such a use cannot be avoided, such dogs may require a reduced dosage and careful clinical management.

Avoid use in any dehydrated, hypoproteinemic, hypovolaemic or hypotensive dog, as there is a potential risk of increased renal toxicity.

NSAIDs can cause inhibition of phagocytosis and hence in the treatment of inflammatory conditions associated with bacterial infection, appropriate concurrent antimicrobial therapy should be instigated.

Refer to section 4.8.

Special precautions to be taken by the person administering the veterinary medicinal product to animals:

In the event of accidental ingestion of the tablets, seek medical advice and show the doctor the package leaflet. Wash hands after handling the product.

4.6 Adverse Reactions (Frequency and Seriousness):

Typical undesirable effects associated with NSAIDs such as vomiting, soft faeces/diarrhoea, faecal occult blood, loss of appetite and lethargy have been reported. These adverse reactions occur generally within the first treatment week and are in most cases transient and disappear following termination of the treatment but in very rare cases may be serious or fatal.

If adverse reactions occur, use of the product should be stopped and the advice of a veterinarian should be sought.

As with other NSAIDs there is a risk of rare renal or idiosyncratic hepatic adverse events.

4.7 Use During Pregnancy, Lactation or Lay:

Studies in laboratory species (rat and rabbit) have shown evidence of foetotoxic effects of carprofen at doses close to the therapeutic dose. The safety of the veterinary medicinal product has not been established during pregnancy and lactation. Do not use in pregnant or lactating bitches.

4.8 Interactions with Other Medical Products and Other Forms of Interaction:

Do not administer NSAIDs and glucocorticoids concurrently or within 24 hours of each other. Some NSAIDs may be highly bound to plasma proteins and compete with other highly bound drugs, which can lead to toxic effects.

Concurrent administration of potential nephrotoxic drugs should be avoided.

4.9 Amounts to be Administered and Administration Route:

For oral administration.

4mg carprofen per kg bodyweight per day.

An initial dose of 4 mg carprofen per kg bodyweight per day given as a single daily dose or in two equally divided doses. The daily dose may be reduced, subject to clinical response.

Duration of treatment will be dependent upon the response seen. Long-term treatment should be under regular veterinary supervision.

To extend analgesic and anti-inflammatory cover post-operatively parenteral pre-operative treatment with an injectable Carprofen product may be followed with Carprogesic 100 mg Tablets at 4mg/kg/day for up to 5 days.

Return any halved tablets to the original pack and use at the next administration

Any halved tablets remaining after the last administration of the product must be discarded

4.10 Overdose (Symptoms, Emergency Procedures, Antidotes), if necessary:

There is no specific antidote for carprofen overdosage but general supportive therapy, as applied to clinical overdosage with NSAIDs should be applied.

4.11 Withhold Period:

Not applicable.

5. Pharmacological Properties

Pharmacotherapeutic group: Non-steroidal anti-inflammatory drug

ATC Vet Code: QM01AE91

5.1 Pharmacodynamic Properties:

Carprofen (CPF), ()-6-chloro--methylcarbazole-2-acetic acid, is a nonsteroidal anti-inflammatory drug (NSAID). It is a derivative of phenylpropionic acid and a member of the arylpropionic acid class of NSAIDs. As a representative of the 2-arylpropionic family, it contains a chiral center at C2of the propionic moiety and therefore, exists in 2 sterioisomeric forms, the (+)-S and (-)-R enantiomers.

Carprofen possess anti-inflammatory, anaglesic and anti-pyretic activity. Carprofen like most other NSAIDs is an inhibitor of the enzyme cyclo-oxygenase of the arachidonic acid cascade. However the inhibition of prostaglandin synthesis by carprofen is slight in relation to its anti-inflammatory and analgesic potency. The precise mode of action of carprofen is not clear.

5.2 Pharmacokinetic Properties:

Absorption is rapid with >90% absorption after oral administration. The volume of distribution is small and carprofen is highly bound to plasma proteins. Biotransformation of carprofen occurs in the liver to form the ester glucuronide and two 1-O-acyl-β-D-glucuronide diastereoisomers. These are secreted in the biliary tract and excreted in the faeces. The Cmaxis 28.51 µg/ml and the AUC is 237.33 µg/ml.hour.

6. Pharmaceutical Particulars

6.1 List of Excipients:

Tartrazine (E102)

Microcrystalline Cellulose

Lactose Monohydrate

Croscarmellose sodium

Povidone K30

Sodium laurilsulphate

Magnesium Stearate

6.2 Incompatibilities:

Not Applicable.

6.3 Shelf-Life:

Shelf life of the veterinary medicinal product as packaged for sale: 2 years

6.4 Special Precautions for Storage:

Do not store above 25ºC.

Store in a dry place.

Protect from light.

6.5 Nature and Composition of Immediate Packaging:

Carprogesic 100mg Tablets are supplied in either:

Polypropylene Snap Secure Tubs containing 14, 30 or 100 tablets, sealed with a white low density Polyethylene Snap Secure Cap, or

Aluminium-Aluminium blister strips of 10 tablets in cartons containing 10, 20, 30, 50, 60, 70, 100, 140, 180, 200, 250, 280, 300, 500 or 1000 tablets.

Not all pack sizes may be marketed

6.6 Special Precautions for the Disposal of Unused Veterinary Medicinal Product or Waste Materials Derived From the Use of Such Products:

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.

7. Marketing Authorisation Holder

Norbrook Laboratories Limited

Station Works

Camlough Road


Co. Down, BT35 6JP

Northern Ireland

8. Marketing Authorisation Number


9. Date of First Authorisation

Date:05 August 2009

10. Date of Revision of the Text

Date: August 2014

Approved: 01/08/2014

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