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POM-VPS Prescription Required

Eraquell 18.7 mg/g Oral Paste

Active ingredient: Ivermectin

Form

Paste

Species

Horses

Manufacturer

VIRBAC

VMD MA No.

05653/3013

What it's used for

Large strongyles: Strongylus vulgaris: adults and 4 th larval (arterial) stages Strongylus edentatus: adults and 4 th larval (tissue) stages Strongylus equ...

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

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

Clinical information

Eraquell 18.7 mg/g Oral Paste — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 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
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
Posology:
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 veterinary medicinal product and 20 mg of ivermectin).
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:
To ensure a correct dosage, body weight should be determined as accurately as possible.
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 dogs or cats as severe adverse reactions may occur.
Do not use in cases of known hypersensitivity to the active substance or to any of the
excipients.
See also section 3.12 “Withdrawal periods”.
Horses:
Undetermined Frequency (cannot be
estimated from the available data)
Swelling
*
Itching
*
*
For some horses carrying heavy infection of microfilariae and 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.
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.
Strategies that should be avoided because they might lead to an increased risk of
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 veterinary medicinal 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.

Special precautions for safe use in the target species:
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.
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.
Special precautions for the protection of the environment:
As ivermectin is extremely dangerous to fish and aquatic life treated animals should not
have direct access to surface water and ditches during treatment.
Other precautions:
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).
The effects of GABA agonists are increased by ivermectin.
Do not store above 30°C.
Store in the original package.
Strategies that should be avoided because they might lead to an increased risk of
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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