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POM-VPS Prescription Required

Chanaverm 7.5% Oral Solution

Active ingredient: Levamisole Hydrochloride

Form

Liquid

Species

Cattle Sheep

Manufacturer

Chanelle Pharmaceuticals Manufacturing Ltd

VMD MA No.

08749/3025

What it's used for

A broad spectrum anthelmintic for the treatment and control of gastro-intestinal and pulmonary nematode infections in cattle and sheep, effective against m...

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

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Paying less for Levamisole Hydrochloride

  1. 1

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    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  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

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Clinical information

Chanaverm 7.5% Oral Solution — SPC Details

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

A broad spectrum anthelmintic for the treatment and control of gastro-intestinal
and pulmonary nematode infections in cattle and sheep, effective against
mature and developing immature stages of the following levamisole-susceptible
major nematode worm species:
Gastro-intestinal Worms: Trichostrongylus spp., Ostertagia
spp. (except inhibited Ostertagia larvae in cattle), Haemonchus
Nematodirus spp., Bunostomum spp., Oesophagostomum spp., spp.
Lungworms: Dictyocaulus spp.
Not effective against Type II winter scour.
The product should only be administered as an oral drench. The 500 ml Armadose
presentation is for use only with the Armadose worming system. The 1L, 2.5L and
5L presentations are for use with conventional dosing gun systems. Dosing should
be carried out accurately, at a dose rate of 7.5 mg Levamisole HCl per 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.
Dosage guide:
Cattle: 1 ml/10 kg bodyweightSheep: 0.5 ml/5 kg bodyweightBodyweightDose (ml)BodyweightDose
(ml)
50 kg (approx. 1 cwt)510 kg (approx. 22 lb)1100 kg (approx. 2 cwt)1020 kg (approx. 44 lb)2150 kg (approx. 3 cwt)1530 kg (approx. 66 lb)3200 kg (approx. 4 cwt)2040 kg (approx. 88 lb)4250 kg (approx. 5 cwt)2550 kg (approx. 110 lb)5300 kg (approx. 6 cwt)3060 kg (approx. 132 lb)6Cattle over 300 kg
should be given a
further 1 ml for each
additional 10 kg
bodyweight
Sheep over 60 kg
should be given a
further 0.5 ml for each
additional 5 kg
bodyweight
Veterinary advice should be sought:
a) on appropriate dosing programmes and stock management to achieve
adequate parasite control, and to reduce the likelihood of anthelmintic
resistance developing.
b) if the product does not achieve the desired clinical effect, since other diseases,
nutritional disturbances or anthelmintic resistance may be involved.
Do not mix with other products.

Revised: September 2025
AN: 01687/2025
Animals should not be treated simultaneously or within 14 days before or after use
with Organophosphorous compounds or diethylcarbamazine citrate.

Revised: September 2025
AN: 01687/2025
Occasionally at the recommended dose cattle may show signs of lip-licking and
slight muscle tremor.
The product may be given to young, pregnant and lactating animals, but due
regard must always be paid to the animals physical condition and the presence of
inter-current disease. When a dosing gun is used to administer the product, care
should be taken to avoid the occurrence of dosing gun pharyngitis.
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:
•
an extended period of time.
•
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 (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.
Resistance to levamisole has been reported in Teladorsagia, Cooperia and
Trichostrongylus species in sheep. There are reports of resistance in
Haemonchus in sheep in various parts of the world other than the EU. Resistance
to levamisole has been reported in Teladorsagia species in cattle in New Zealand.
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.

i. Special precautions for use in animals
Care should be taken to accurately estimate the bodyweight of animals to
be treated before calculating the dose.
For oral use only
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Levamisole can cause idiosyncratic reactions as well as serious blood
disorders in a very small number of people. If symptoms such as
dizziness, nausea or vomiting or abdominal discomfort are experienced
when using this product, or sore mouth /throat or fever occur shortly
afterwards, then medical advice should be sought immediately. Wash
hands and exposed skin before meals and after work. Remove
immediately any contaminated clothing. Wash splashes from eyes and
skin immediately. If irritation persists, consult your doctor. When using do
not eat, drink or smoke.

Revised: September 2025
AN: 01687/2025
See 4.3 (2).
Animals must not be slaughtered for human consumption during treatment. Cattle
and sheep may be slaughtered for human consumption only after 20 days from the
last treatment.
Not for use in animals producing milk 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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