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POM-VPS Prescription Required

Vimectanin DUO 50 mg/ml + 1 mg/ml Oral Suspension for Sheep

Active ingredients: Ivermectin, Triclabendazole

Form

Liquid

Species

Sheep

Manufacturer

Pharma VIM Kft.

VMD MA No.

59599/5000

What it's used for

Strongyloides papillosus Oesophagostomum spp and adult - of age): Fasciola hepatica - Dictyocaulus filarial - Oestrus ovis

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

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  1. 1

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  2. 2

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    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Vimectanin DUO 50 mg/ml + 1 mg/ml Oral Suspension for Sheep — SPC Details

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

Strongyloides papillosus
Oesophagostomum spp
and adult
-
of age):
Fasciola hepatica
-
Dictyocaulus filarial
-
Oestrus ovis
The recommended dose rate is 0.2 mg ivermectin and 10 mg triclabendazole/kg
bodyweight, equivalent to 2 ml of the product per 10 kg bodyweight.
Underdosing could result in ineffective use and may favour resistance development.
To ensure a correct dosage, bodyweight 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.
The product is for oral administration using a suitably calibrated dosing gun. Accuracy
of the dosing device should be thoroughly checked. The container should be shaken
for 1 minute before use. Drenching equipment should be cleaned before and after use.
The timing for treatment should be based on epidemiological factors and should be
customised for each individual farm. As with other anthelmintics, veterinary advice
should be sought on appropriate dosing programmes and stock management to
achieve adequate parasite control and reduce the likelihood of resistance developing.
For infections with parasites listed at the indications, the need for and frequency of re-
treatment(s) should be based on professional advice and should take into account the
local epidemiological situation and the animal’s lifestyle.
Dosing table:
Animal weightDose of the
product
20 – 25 kg5 ml26 – 30 kg6 ml31 – 35 kg7 ml36 – 40 kg8 ml41 – 50 kg10 ml51 – 60 kg12 ml61 – 70 kg14 ml71 – 80 kg16 ml81 – 90 kg18 ml91 – 100 kg20 ml
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
None 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.
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 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 herd.
Repeated use for an extended period, particularly when using the same class of
substances, increases the risk of resistance development. Within a herd,
maintenance of susceptible refugia is essential to reduce that risk. Systematically
applied interval-based treatment and treatment of a whole herd should be avoided.
Instead, if feasible, only selected individual animals or subgroups should be treated
(targeted selective treatment). This should be combined with appropriate husbandry
and pasture management measures. Guidance for each specific herd should be
sought from the responsible veterinarian.
In the absence of risk of co-infection of nematodes, trematodes and nasal bots, a
narrow spectrum product should be used.
In sheep, resistance to ivermectin is widespread in Teladorsagia circumcincta,
Trichostrongylus spp., Haemonchus contortus and in other gastro-intestinal parasite
species.
Multiple resistance was reported in Teladorsagia circumcincta
macrocyclic lactones and levamisole and in Haemonchus contortus to ivermectin
and benzimidazoles.
Resistance to triclabendazole has been reported in Fasciola hepatica in sheep.
The use of this product should take into account local information about susceptibility
of the target parasites, where available.
It is recommended to further investigate cases of suspected resistance, using an
appropriate diagnostic method (e.g. Faecal Egg Count Reduction test, FECR test).
Confirmed resistance should be reported to the marketing authorisation holder or to
the competent authorities.

Special precautions for safe use in the target species:
Not applicable.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
The veterinary medicinal product may cause hypersensitivity (allergic reactions).
People with known hypersensitivity to the active substances or to any of the excipients
should avoid contact with the veterinary medicinal product.
This veterinary medicinal product may cause skin and eye irritation.
Direct contact with the skin should be kept to a minimum. Personal protective
equipment consisting of gloves should be worn when handling the veterinary medicinal
product.
In case of accidental spillage onto skin or into the eyes, wash immediately with plenty
of water. Take off any contaminated clothes.
Do not eat, drink or smoke whilst handling the veterinary medicinal product. Wash
hands thoroughly after use.
Special precautions for the protection of the environment:
Ivermectin is highly toxic to aquatic organisms, and ivermectin and triclabendazole
are highly toxic to dung flies and beetles. Long-term effects on dung insects caused
by continuous or repeated use cannot be excluded.
The risk to aquatic ecosystems and dung fauna can be reduced by avoiding too
frequent and repeated use of this product and other products of the same
anthelmintic class in cattle, sheep and pigs. Therefore repeated treatment of
animals on a pasture with an ivermectin-containing product within a season should
only be given in the absence of alternative treatments or approaches to maintain
animal/flock health, as advised by a veterinarian.
Other precautions:
Extra-label use in dogs should be avoided as severe adverse reactions may occur.
Certain breeds of dogs, such as Collies, their related breeds and their mixes are
especially sensitive to ivermectin and particular care should be taken to avoid
accidental consumption of the product.
No data available.
Store in the original package.
Do not refrigerate. Protect from frost.
Meat and offal: 27 days.
Not authorised for use in animals producing milk for human consumption, including
during the dry period.
Do not use within 1 year prior to the first lambing in ewes intended to produce milk
for human consumption.

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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