Profender 50 mg/10 mg Modified-Release Tablets for Medium Dogs
Active ingredients: Emodepside, Praziquantel
Form
Tablet
Species
Manufacturer
Vetoquinol SA
VMD MA No.
06462/5008
What it's used for
For dogs, when mixed parasitic infections caused by roundworms and coccidia of the following species are suspected or demonstrated: Roundworms (Nematodes):...
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Profender 50 mg/10 mg Modified-Release Tablets for Medium Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
following species are suspected or demonstrated:
Roundworms (Nematodes):
- (mature adult, immature adult, L4)
-
-
- (mature adult)
Coccidia:
-complex
-
Revised: November 2023
AN: 01821/2023
Procox is effective against the replication of Isospora and also against the shedding
of oocysts. Although treatment will reduce the spread of infection, it will not be
effective against the clinical signs of infection in already infected animals.
Body
weight
(kg)
Number of modified-release tablets forsmall dogs
1 = 3
medium dogs
1 =
10 kg
large dogs
1 =
30 kg
1 - 1.5½> 1.5 - 31> 3 - 4.51½> 4.5 - 62> 6 - 101> 10 - 151½> 15 - 202> 20 - 301> 30 - 451½> 45 - 602
Method of administration
For oral use in dogs from 12 weeks of age and weighing at least 1 kg. The veterinary
medicinal product tablets are meat flavoured and usually dogs will accept them
without any food.
Administer only to fasted dogs. For example: Overnight fasting if the dog is to be
treated in the morning. No food should be given until 4 hours after treatment.
Underdosing could result in ineffective use and may favour resistance development
To ensure a correct dosage, body weight should be determined as accurately as
possible. If animals are to be treated collectively, reasonably homogeneous groups
should be set up, and all animals of a group should be dosed at the rate
corresponding to the heaviest one.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
Very rare
(< 1 animal / 10,000 animals
treated, including isolated
reports):
Digestive tract disorders
(e.g. hypersalivation,
vomiting, diarrhoea)
Neurological disorders
1,2
(e.g. tremor,
incoordination)
1,2
, Convulsion
Behavioural disorders (e.g. hyperactivity)
Anorexia, lethargy, recumbency, hyperthermia.
Mild and transient
Non-compliance with fasting requirements tended to be a feature of those cases
Signs of neurological disorders may be more severe in mdr1 mutant (-/-) Collies,
Shelties and Australian Shepherds. Specific antidotes are not known
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.
frequent, repeated use of an anthelmintic of that class.
Unnecessary use of antiparasitics or use deviating from the instructions given in the
SPC may increase the resistance selection pressure and lead to reduced efficacy.
The decision to use the veterinary medicinal product should be based on
confirmation of the parasitic species and burden, or of the risk of infection based on
its epidemiological features, for each individual animal.
The possibility that other animals in the same household can be a source of re-
infection with roundworms and tapeworms should be considered, and these should
be treated as necessary with an appropriate veterinary medicinal product.
Special precautions for safe use in the target species:
Administer only to fasted dogs. For example: Overnight fasting if the dog is to be
treated in the morning. No food should be given until 4 hours after treatment.
When D. caninum infection is present, concomitant treatment against intermediate
hosts such as fleas and lice should be considered to prevent reinfection.
No studies have been performed with severely debilitated dogs or individuals with
seriously compromised kidney or liver function. Therefore, the veterinary medicinal
product should only be used in such animals according to a benefit/risk assessment
by the responsible veterinarian.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
In the interests of good hygiene, wash your hands after administering the tablets to
the dog.
In case of accidental ingestion, especially in the case of children, seek medical
advice immediately and show the package leaflet or the label to the physician.
Echinococcosis represents a hazard for humans. As Echinococcosis is a notifiable
disease to the World Organisation for Animal Health (WOAH), specific guidelines on
the treatment and follow-up, and on the safeguard of persons, need to be obtained
from the relevant competent authority.
Special precautions for the protection of the environment:
Not applicable.
P-glycoprotein substrates/inhibitors (for example, ivermectin and other antiparasitic
macrocyclic lactones, erythromycin, prednisolone and cyclosporine) could give rise to
pharmacokinetic drug interactions. The potential clinical consequences of such
interactions have not been investigated.
Any unused half tablet should be discarded.
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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Related Conditions
Other Products Containing Emodepside
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Beaphar WORMclear PLUS 30 mg/7.5 mg Spot-on Solution for Small Cats
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Beaphar WORMclear PLUS 30 mg/7.5 mg Spot-on Solution for Small Cats
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Beaphar WORMclear PLUS 96 mg/24 mg Spot-on Solution for Large Cats
NFA-VPSKRKA, d.d., Novo mesto
Beaphar WORMclear PLUS 96 mg/24 mg Spot-on Solution for Large Cats
NFA-VPSKRKA, d.d., Novo mesto
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