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POM-VPS Prescription Required

Animec 0.8mg/ml Oral Solution for Sheep

Active ingredient: Ivermectin

Form

Liquid

Species

Sheep

Manufacturer

Chanelle Pharmaceuticals Manufacturing Ltd

VMD MA No.

08749/4027

What it's used for

For the treatment of infections with the following parasites: Nematodes Gastrointestinal roundworms (adult and fourth larval stage) Haemonchus contortus Te...

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

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Paying less for Ivermectin

  1. 1

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  2. 2

    Fill it at a registered online retailer

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

Prescription required

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Clinical information

Animec 0.8mg/ml Oral Solution for Sheep — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

For the treatment of infections with the following parasites:
Nematodes
Gastrointestinal roundworms (adult and fourth larval stage)
Haemonchus contortus
Teladorsagia circumcincta
Trichostrongylus spp.
Cooperia spp.
Nematodirus spp.
Including N. battus
Strongyloides papillosus
Chabertia ovina
Lungworms(adult and fourth larval stage)
Dictyocaulus filaria

Revised: October 2014
AN: 00740/2014
Arthropods
Nasal bot (all larval stages)
Oestrus ovis
For oral administration only.
The recommended dose rate is 0.2 mg ivermectin per kg bodyweight
(corresponding to 2.5 ml per 10 kg bodyweight)
To ensure administration of a correct dose, body weight should be determined as
accurately as possible. Accuracy of the dosing device should be checked.
If animals are to be treated collectively rather than individually they should be
grouped according to their bodyweight and dosed accordingly, in order to avoid
under- or over- dosing.
Do not use in animals with known hypersensitivity to the active ingredient or any
of the excipients.
Some sheep may cough immediately after treatment. This passing response is of
no consequence.
Care should be taken to avoid the following practices because they increase the
risk of development of resistance and could ultimately result in ineffective therapy:
• Too frequent and repeated use of anthelmintics from the same class, over
an extended period of time.
• Underdosing, which may be due to underestimation of body weight or
misadministration of the product.
 
Resistance to ivermectin (an avermectin) has been reported in Teladorsagia in
sheep and goats within the EU and it is common in Haemonchus in sheep outside
the EU. Therefore the use of this product should be based on local (regional,
farm) epidemiological information about susceptibility of nematode and
recommendations on how to limit further selection for resistance to anthelmintics.
Suspected clinical cases of resistance to anthelmintics should be further
investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test).
Where the results of the test(s) strongly suggest resistance to a particular
anthelmintic, an anthelmintic belonging to another pharmacological class and
having a different mode of action should be used.
There is cross-resistance with other avermectins and with milbemycins.

i. Special precautions for use in animals
The timing of treatment should be based on epidemiological factors and
should be customised for each individual farm. A dosing programme should
be established by the veterinary surgeon.
Veterinary advice should be sought on appropriate dosing programmes and
stock management to achieve adequate parasite control, and to reduce the
likelihood of anthelmintic resistance developing. Veterinary advice should
also be sought if the product does not achieve the desired clinical effect, as
other diseases, nutritional disturbances or anthelmintic resistance might be
involved.
Avermectins may not be well tolerated in non-target species. Cases of
intolerance resulting in fatalities have been reported in dogs, especially
Collies, Old English Sheep Dogs and related breeds or crosses, and also in
turtles/tortoises.

Revised: October 2014
AN: 00740/2014
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Wash hands after use. Avoid contact with skin and eyes.
Do not eat, drink or smoke while handling the product.
Wear impervious gloves when handling or administering the product.
As absorption through skin can occur, in the event of accidental skin
contact, wash the affected area immediately with soap and water.
If accidental eye exposure occurs, flush the eyes immediately with water.
iii. Other precautions
None known.
None known.
None known.

4.9 Amounts to be administered and administration route
For oral administration only.
The recommended dose rate is 0.2 mg ivermectin per kg bodyweight
(corresponding to 2.5 ml per 10 kg bodyweight)
To ensure administration of a correct dose, body weight should be determined as
accurately as possible. Accuracy of the dosing device should be checked.
If animals are to be treated collectively rather than individually they should be
grouped according to their bodyweight and dosed accordingly, in order to avoid
under- or over- dosing.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
At doses up to 4 mg ivermectin per kg administered by stomach tube (20x the
recommended dose level) undesirable toxic reactions occurred. Acute symptoms
(ataxia, staggering gait, incoordination, depression) were observed at the dose
rate of 8 mg/kg (40x the recommended dose level) during a study carried out on 4
animals. Twenty-four hours later, the animals showed only mild incoordination
and depression.

Revised: October 2014
AN: 00740/2014
Three days post dose all the animals were nearly normal. It is possible that the
signs of toxaemia were due to the propylene glycol.
No antidote has been identified. Symptomatic treatment may be beneficial.
4.11 Withdrawal periods
Meat and offal: 10 days.
Milk: Do not use in lactating sheep producing milk for human consumption.
Sheep must not be treated within 60 days prior to the commencement of lactation,
if milk is to be used for human consumption.
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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