Convenia 80 mg/ml Powder and Solvent for Solution for Injection for Dogs and Cats
Active ingredient: Cefovecin
Form
Injection
Species
Manufacturer
Zoetis Belgium
VMD MA No.
EU/2/06/059/001-002
What it's used for
For use only for the following infections which require prolonged treatment. The antimicrobial activity of the veterinary medicinal product following a sin...
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Convenia 80 mg/ml Powder and Solvent for Solution for Injection for Dogs and Cats — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
antimicrobial activity of the veterinary medicinal product following a single injection
lasts for up to 14 days.
Dogs:
For the treatment of skin and soft tissue infections including pyoderma, wounds and
abscesses associated with Staphylococcus pseudintermedius, -haemolytic
Streptococci, Escherichia coli and/or .
For the treatment of urinary tract infections associated with Escherichia coli and/or
Proteus spp.
Amended pages: March 2025
AN: 02825/2023 & AN: 01472/2024
As adjunctive treatment to mechanical or surgical periodontal therapy in the
treatment of severe infections of the gingiva and periodontal tissues associated with
Porphyromonas spp. and Prevotella spp. (see also Section 4.5 ‘Special Precautions
for Use’.)
Cats:
For the treatment of skin and soft tissue abscesses and wounds associated with
Pasteurella multocidaFusobacterium spp., Bacteroides spp., Prevotella oralis, -
haemolytic Streptococci and/or Staphylococcus pseudintermedius.
For the treatment of urinary tract infections associated with Escherichia coli.
any of the excipients.
Do not use in small herbivores (including guinea pigs and rabbits).
Do not use in dogs and cats less than 8 weeks old.
Very rare (<1 animal /
10,000 animals treated,
including isolated reports):
Injection site reaction
Digestive tract disorder (e.g. diarrhoea, emesis,
anorexia)
Hypersensitivity reaction (e.g. anaphylaxis,
circulatory shock, dyspnoea)
Neurological signs (e.g. ataxia, convulsion,
seizure)
Appropriate treatment should be administered without delay.
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.
other -lactam antibiotics. Use of the veterinary medicinal product should be
carefully considered when susceptibility testing has shown resistance to
cephalosporins or -lactams because its effectiveness may be reduced.
Special precautions for use in animals
Use of the product should be based on identification and susceptibility testing of the
target pathogen(s). If this is not possible, therapy should be based on
epidemiological information and knowledge of susceptibility of the target pathogens
at local/regional level. Use of the product should be in accordance with official,
national and regional antimicrobial policies.
An antibiotic with a lower risk of antimicrobial resistance selection (lower AMEG
category) should be used for first line treatment where susceptibility testing suggests
the likely efficacy of this approach.
The product selects for resistant strains such as bacteria carrying extended-
spectrum beta-lactamases (ESBL) and may constitute a risk to human health if these
strains disseminate to humans.
The fundamental requirement of the treatment of periodontal disease is mechanical
and/or surgical intervention by the veterinarian.
The safety of the veterinary medicinal product has not been assessed in animals
suffering from severe renal dysfunction.
Amended pages: March 2025
AN: 02825/2023 & AN: 01472/2024
Pyoderma is often secondary to an underlying disease. It is, therefore, advisable to
determine the underlying cause and to treat the animal accordingly.
Caution should be exercised in patients that have previously shown hypersensitivity
reactions to cefovecin, other cephalosporins, penicillins, or other medicinal products.
If an allergic reaction occurs, no further administrations of cefovecin should be
administered and appropriate therapy for beta-lactam hypersensitivity should be
instituted. Serious acute hypersensitivity reactions may require treatment with
epinephrine and other emergency measures, including oxygen, intravenous fluids,
intravenous antihistamine, corticosteroids, and airway management, as clinically
indicated. Veterinarians should be aware that reappearance of the allergic symptoms
may occur when symptomatic therapy is discontinued.
Occasionally, cephalosporins have been associated with myelotoxicity, thereby
creating a toxic neutropenia. Other haematological reactions seen with
cephalosporins include neutropenia, anaemia, hypoprothrombinemia,
thrombocytopenia, prolonged prothrombin time (PT) and partial thromboplastin time
(PTT), platelet dysfunction.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Penicillins and cephalosporins may cause hypersensitivity (allergy) following
injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead
to cross sensitivity to cephalosporins and vice versa. Allergic reactions to these
substances may occasionally be serious.
Do not handle this product if you know you are sensitised or if you have been
advised not to work with such preparations.
Handle this product with care to avoid exposure, taking all recommended
precautions.
If you develop symptoms following exposure, such as a skin rash, you should seek
medical advice and show the doctor this warning. Swelling of the face, lips or eyes or
difficulty in breathing are more serious symptoms and require urgent medical
attention.
If you know you are allergic to penicillins or cephalosporins, avoid contact with
contaminated litter. In the event of contact, wash skin with soap and water.
Special precautions for the protection of the environment
Not applicable.
Other precautions
Not applicable.
Amended pages: March 2025
AN: 02825/2023 & AN: 01472/2024
furosemide, ketoconazole, or non-steroidal anti-inflammatory drugs (NSAIDs)) may
compete with cefovecin binding and thus may cause adverse events.
Store in a refrigerator (2 C – 8 C). Do not freeze.
Store in the original package in order to protect from light.
After reconstitution:
Store in a refrigerator (2 C – 8 C). Do not freeze.
Store in the original package in order to protect from light.
AN: 02825/2023 & AN: 01472/2024
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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Related Conditions
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