Eraquell 18.7 mg/g Oral Paste
Active ingredient: Ivermectin
Form
Paste
Species
Manufacturer
VIRBAC
VMD MA No.
05653/5043
What it's used for
Roundworms in the stomach and intestines. Large strongyles: Strongylus vulgaris: adults and 4 th larval (arterial) stages Strongylus edentatus: adults and...
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Prescription required
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Eraquell 18.7 mg/g Oral Paste — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
Large strongyles:
Strongylus vulgaris: adults and 4
th
larval (arterial) stages
Strongylus edentatus: adults and 4
th
larval (tissue) stages
Strongylus equinus: adults
Small strongyles, adults:
Cyathostomum spp.
Cylicocyclus spp.
Cylicodontophorus spp.
Cylicostephanus spp.
Gyalocephalus spp.
Hairworms:
Trichostrongylus axei: adults
Pinworms:
Oxyuris equi: adults and immatures
Ascarids:
Parascaris equorum: adults
Revised: October 2024
MA split from NI MA following AN: 03943/2022
Intestinal threadworms:
Strongyloides westeri: adults
Large-mouth stomach worms:
Habronema muscae: adults
Neck threadworms:
Onchocerca
Lungworms:
Dictyocaulus arnfieldi:
Stomach bots:
Gasterophilus spp.: oral and gastric larval stages
A single administration of 200 µg ivermectin per kg of bodyweight.
Each syringe division mark plunger delivers enough paste to treat 100 kg of
bodyweight (which corresponds to 1.07 g of product and 20 mg of ivermectin).
Revised: October 2024
MA split from NI MA following AN: 03943/2022
The syringe containing 6.42 g of paste delivers sufficient paste to treat 600 kg of
bodyweight at the recommended dose range.
The syringe containing 7.49 g of paste delivers sufficient paste to treat 700 kg of
bodyweight at the recommended dose range.
Directions for use
Horse weight should be accurately determined for the correct use of the paste. The
animal's mouth should be free of food. The syringe must be positioned between the
front and back teeth and the paste must be placed on the base of the horse’s
tongue. Immediately elevate the head of the horse for a few seconds to ensure
deglutition.
Re-treatment should be done according to the epidemiological situation, but not at
less than 30 days interval.
Do not use in cases of known hypersensitivity to the active substance.
See also section 4.11 “Withdrawal periods”.
experienced reactions with swelling and itching following dosing, assumed to be the
result of death of large numbers of microfilariae.
These signs resolve within a few days but symptomatic treatment may be advisable.
development of resistance to anthelmintic drugs include:
• 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,
misadministration of the product, or lack of calibration of the dosing device (if
any).
Suspected clinical cases of resistance to anthelmintics should be further
investigated using appropriate tests. 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.
Resistance to ivermectin has been reported in Parascaris equorum in horses.
Therefore the use of this product should be based on local (regional, farm)
epidemiological information about susceptibility of nematodes and
recommendations on how to limit further selection for resistance to anthelmintics.
Revised: October 2024
MA split from NI MA following AN: 03943/2022
i. Special precautions for use in animals
Avermectins may not be well tolerated in all non-target species (cases of
intolerance with fatal outcome are reported in dogs, especially Collies, Old
English Sheepdogs and related breeds or crosses, and also in
turtles/tortoises).
As ivermectin is extremely dangerous to fish and aquatic life treated animals
should not have direct access to surface water and ditches during treatment.
Parasite resistance to any particular class of anthelmintic may develop
following frequent, repeated use of an anthelmintic of that class.
Since ivermectin is highly bound to plasma proteins, special care should be
taken in cases of sick animals or in nutritional conditions associated with low
plasma protein levels.
As with all anthelmintics, a veterinary surgeon should establish appropriate
dosing programs and stock management to achieve adequate parasite control
and reduce the likelihood of anthelmintic resistance.
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Do not eat, drink or smoke while handling the product. Avoid contact with skin
and eyes. If accidental skin contact occurs, wash the affected area
immediately with soap and water. If accidental eye exposure occurs, flush the
eyes immediately with water and, if necessary, get medical attention.
Wash hands after use.
Store in the original packaging.
development of resistance to anthelmintic drugs include:
• 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,
misadministration of the product, or lack of calibration of the dosing device (if
any).
Suspected clinical cases of resistance to anthelmintics should be further
investigated using appropriate tests. Where the results of the test(s) strongly
suggest resistance to a particular anthelmintic, an anthelmintic belonging to another
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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