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POM-V Prescription Required Companion Animal

Pramilon 12.5 mg/125 mg Film-coated Tablets for Dogs

Active ingredients: Milbemycin Oxime (A3 and A4), Praziquantel

Form

Tablet

Species

Dogs

Manufacturer

Alfamed

VMD MA No.

17902/3006

What it's used for

Mesocestoides spp. Nematodes: Ancylostoma caninum, Toxocara canis, Toxascaris leonina, Trichuris vulpis, Thelazia callipaeda (see specific treatment schedu...

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

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Prescription required

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Clinical information

Pramilon 12.5 mg/125 mg Film-coated Tablets for Dogs — SPC Details

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

Mesocestoides spp.
Nematodes:
Ancylostoma caninum,
Toxocara canis,
Toxascaris leonina,
Trichuris vulpis,
Thelazia callipaeda (see specific treatment schedules under section 3.9
“Administration routes and dosage”),
Crenosoma vulpis (reduction of the level of infection),
Angiostrongylus vasorum (reduction of the level of infection by immature adult (L5)
and adult parasite stages; see specific treatment and disease prevention
schedules under section 3.9 “Administration routes and dosage”).
The veterinary medicinal product can also be used in the prevention of heartworm
disease (Dirofilaria immitis), if concomitant treatment against cestodes is indicated.
Minimum recommended dose rate: 0.5 mg of milbemycin oxime and 5 mg of
praziquantel per kg given once orally.
To ensure a correct dosage, body weight should be determined as accurately as
possible.

Revised July 2025
The veterinary medicinal product should be administered with or after some food.
The tablets are meat-flavoured and easy to administer (usually dogs and puppies will
accept them voluntarily even without any food).
Depending on the body weight of the dog, the practical dosing is as follows:
WeightTablets5 – 25 kg1 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 product for the prevention of heartworm disease.
For treatment of 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 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 , milbemycin oxime should be given in 2
treatments, seven days apart. Where concomitant treatment against cestodes is
indicated, the veterinary medicinal product can replace the monovalent product
containing milbemycin oxime alone.
Do not use in dogs weighing less than 5 kg.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
See also section “Special precautions for use”.
Dogs:
Very rare
(< 1 animal / 10,000 animals
treated, including isolated
reports):
Hypersensitivity reaction
Systemic disorder (e.g. Lethargy and Anorexia)
Neurological disorder (e.g. Muscle tremors,
Ataxia and Convulsions)
Digestive tract disorder (e.g. Emesis,
Diarrhoea, and Drooling)
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 its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.
In order to develop an effective worm control programme, local epidemiological
information and the living conditions of the dog should be taken into account and
therefore it is recommended to seek professional advice.
Parasite resistance to any particular class of anthelmintic may develop following
frequent, repeated use of an anthelmintic of that class.
It is recommended to treat all the animals in the same household concomitantly.
When infection is present, concomitant treatment against
intermediate hosts, such as fleas and lice, should be considered to prevent re-infection.

Revised July 2025

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 also section 3.10).
As per good veterinary practice, animals should be weighed to ensure accurate dosing.
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 the 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 product may therefore not be necessary.
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:
Wash hands after use.
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:
Not applicable.

Revised July 2025
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.
The concurrent use of the combination praziquantel/milbemycin oxime with selamectin
is well tolerated. No interactions were observed when the recommended dose of the
macrocyclic lactone selamectin was administered during treatment with the combination
at the recommended dose. In the absence of further studies, caution should be taken in
the case of concurrent use of the veterinary medicinal product and other macrocyclic
lactones. Also, no such studies have been performed with reproducing animals.
Keep the blister in the outer carton.
This veterinary medicinal product does not require any special temperature storage
conditions.
Not applicable.

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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