MilbeVet 12.5 mg/125 mg Chewable Tablets for Dogs
Active ingredients: Milbemycin Oxime (A3 and A4), Praziquantel
Form
Chewable
Species
Manufacturer
Elanco GmbH
VMD MA No.
52127/3032
What it's used for
This veterinary medicinal product is only indicated when use against cestodes and nematodes or prevention of heartworm disease/angiostrongylosis is indicat...
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MilbeVet 12.5 mg/125 mg Chewable Tablets for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
nematodes or prevention of heartworm disease/angiostrongylosis is indicated at the
same time.
AN: 00219/2025Page 2 of 8
Cestodes
Treatment of tapeworms: Dipylidium caninum, Taenia sppspp.,
Mesocestoides spp.
Gastrointestinal nematodes
Treatment of:
Hookworm: Ancylostoma caninum,
Roundworms: Toxocara canis, Toxascaris leonina,
Whipworm:.
Eyeworm
Treatment of Thelazia callipaeda (see specific treatment schedule under section 3.9
“Administration routes and dosage”).
Lungworms
Treatment of:
Angiostrongylus vasorum (Reduction of the level of infection by immature adult (L5)
and adult parasite stages; see specific treatment and prevention disease schedules
under section 3.9 “Administration routes and dosage”),
Crenosoma vulpis (Reduction of the level of infection).
Heartworm
Prevention of heartworm disease (Dirofilaria immitis) if concomitant treatment against
cestodes is indicated.
To ensure a correct dosage, body weight should be determined as accurately as
possible.
Minimum recommended dose rate: 0.5 mg of milbemycin oxime and 5 mg of
praziquantel per kg as a single dose. The veterinary medicinal product should be
administered with or after some food.
Depending on the bodyweight of the dog, the practical dosing is as follows:
WeightNumber of Tablet 5 – 25 kg 1 tablet > 25 - 50 kg2 tablets > 50 - 75 kg3 tablets
In cases when heartworm disease prevention is used and at the same time treatment
against tapeworm is required, the veterinary medicinal product can replace the
monovalent veterinary medicinal product for the prevention of heartworm disease.
For treatment of Angiostrongylus vasorum infections, milbemycin oxime should be
given four times at weekly intervals. It is recommended, where concomitant treatment
against cestodes is indicated, to treat once with the veterinary medicinal product and
continue with the monovalent veterinary medicinal product containing milbemycin
oxime alone, for the remaining three weekly treatments.
In endemic areas administration of the veterinary medicinal product every four weeks
will prevent angiostrongylosis by reducing immature adult (L5) and adult parasite
burden, where concomitant treatment against cestodes is indicated.
For the treatment of Thelazia callipaeda
treatments, seven days apart. Where concomitant treatment against cestodes is
indicated, the veterinary medicinal product can replace the monovalent veterinary
medicinal product containing milbemycin oxime alone.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
See also section 3.5 "Special precautions for use".
Very rare
(<1 animal / 10 000 animals
treated, including isolated
reports):
Digestive tract disorders (such as Diarrhoea,
Drooling, Emesis)
Hypersensitivity reaction
Neurological disorders (such as Ataxia,
Convulsions, Muscle tremors)
Systemic disorders (such as Anorexia, Lethargy)
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.
should be considered, and these should be treated as necessary with an appropriate
veterinary medicinal product.
It is recommended to treat all the animals living in the same household
concomitantly.
When infection with the cestode D. caninum has been confirmed, concomitant
treatment against intermediate hosts, such as fleas and lice, should be discussed
with a veterinarian to prevent re-infection.
Parasite resistance to any particular class of anthelmintic may develop following
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 use of the veterinary medicinal product should follow the implementation of
appropriate diagnostic measures towards mixed infections by nematodes and
cestodes with consideration of animal history and characteristics (e.g. age, health
status), environment (e.g. kennelled dogs, hunting dogs), feeding (e.g. access to raw
meat), geographical location and travel. Judgement of the administration of the
AN: 00219/2025Page 3 of 8
veterinary medicinal product in dogs at risk from mixed re-infections or in specific at
risk situations (such as zoonotic risks), should be made by the responsible
veterinarian.
In the absence of risk of co-infection with nematodes or cestodes, a narrow spectrum
veterinary medicinal product should be used.
Resistance of to praziquantel as well as cases of multi-drug
resistance of Ancylostoma caninum to milbemycin oxime and resistance of Dirofilaria
immitis to macrocyclic lactones have been reported.
It is recommended to further investigate cases of suspected resistance, using an
appropriate diagnostic method. Confirmed resistance should be reported to the
marketing authorisation holder or to the competent authorities.
The use of this veterinary medicinal product should take into account local
information about susceptibility of the target parasites, where available.
Special precautions for safe use in the target species:
Studies with milbemycin oxime indicate that the margin of safety in certain dogs of
Collie or related breeds is less than in other breeds. In these dogs, the recommended
dose should be strictly observed.
The tolerance of the veterinary medicinal product in young puppies from these
breeds has not been investigated. Clinical signs in Collies are similar to those seen in
the general dog population when overdosed (see section 3.10 “Overdose”).
Treatment of dogs with a high number of circulating microfilariae can sometimes lead
to the appearance of hypersensitivity reactions, such as pale mucous membranes,
vomiting, trembling, laboured breathing or excessive salivation. These reactions are
associated with the release of proteins from dead or dying microfilariae and are not a
direct toxic effect of the veterinary medicinal product. The use in dogs suffering from
microfilaremia is thus not recommended.
In heartworm risk-areas, or in the case it is known that a dog has been travelling to
and from heartworm risk regions, before using the veterinary medicinal product, a
veterinary consultation is advised to exclude the presence of any concurrent
infestation of Dirofilaria immitis. In the case of a positive diagnosis, adulticidal therapy
is indicated before administering the veterinary medicinal product.
No studies have been performed with severely debilitated dogs or individuals with
seriously compromised kidney or liver function. The veterinary medicinal product is
not recommended for such animals or only according to a benefit/risk assessment by
the responsible veterinarian.
In dogs less than 4 weeks old, tapeworm infection is unusual. Treatment of animals
less than 4 weeks old with a combination veterinary medicinal product may therefore
not be necessary.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Wash hands after use.
People with known hypersensitivity to any of the ingredients should avoid contact
with the veterinary medicinal product.
In case of accidental ingestion of the tablets, particularly by a child, seek medical
advice immediately and show the package leaflet or the label to the physician.
Special precautions for the protection of the environment:
See section 5.5.
AN: 00219/2025Page 4 of 8
Other precautions:
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 (e.g. experts or institutes of parasitology).
lactone selamectin was administered during treatment with the veterinary medicinal
product at the recommended dose.
Although not recommended, the concomitant use of the veterinary medicinal product
with a spot on containing moxidectin and imidacloprid at recommended dose rates
following a single application was well tolerated in one experimental study by beagle
dogs at the age 11 months or older.
Transient neurological adverse reactions (poor proprioception, flaccid frontal and
hind legs, incoordination, slight tremors and high stepping gait of the hind limbs only)
were observed after concurrent administration of both veterinary medicinal products
in another study conducted in puppies aged 8-12 weeks. Such signs were however
not observed in this study after giving the veterinary medicinal product alone.
The safety and efficacy of this combination have not been investigated in field
studies.
In the absence of further studies, caution should be taken in the case of concurrent
use with any other macrocyclic lactone. Also, no such studies have been performed
with breeding animals, Collies, related breeds and their crosses.
AN: 00219/2025Page 5 of 8
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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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Other Products Containing Milbemycin Oxime (A3 and A4)
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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POM-VKRKA, d.d., Novo mesto
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POM-VKRKA, d.d., Novo mesto
Alpramil 12 mg/30 mg Film-coated Tablets for Cats Weighing at Least 3 kg
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POM-VAlfasan Nederland B.V.
Alpramil 12.5 mg/125 mg Tablets for Dogs Weighing at Least 5 kg
POM-VAlfasan Nederland B.V.
Alpramil 12.5 mg/125 mg Tablets for Dogs Weighing at Least 5 kg
POM-VAlfasan Nederland B.V.
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