Levacide 7.5% Solution for Injection for Cattle and Sheep
Active ingredient: Levamisole Hydrochloride
Form
Injection
Species
Manufacturer
Norbrook Laboratories Limited
VMD MA No.
02000/4049
What it's used for
A broad spectrum anthelmintic for use in the treatment and control of nematode infections. It should be used in cases of parasitic gastro-enteritis and lun...
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Prescription required
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Levacide 7.5% Solution for Injection for Cattle and Sheep — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
nematode infections. It should be used in cases of parasitic gastro-enteritis
and lungworm disease caused by mature and developing immature forms of
those organisms sensitive to treatment with levamisole hydrochloride.
bodyweight. Usual aseptic precautions should be observed. Cattle should be
dosed at a rate of 1 ml of product per 10 kg bodyweight and sheep at a rate of
0.5 ml per 5 kg bodyweight. To ensure administration of a correct dose,
bodyweight should be determined as accurately as possible; accuracy of the
dosing device should be checked.
Divide large doses between two or more injection sites. In order to minimise
the risk of infection, needles should be changed frequently.
Do not mix with any other products before administration except if premixing
is done by a veterinary surgeon or a pharmacist.
treatment with organophosphorus compounds.
reaction at the site of injection. This should resolve naturally in a short period
of time.
the risk of development of resistance and could ultimately result in ineffective
therapy:
•
an extended period of time.
Revised: July 2010
(ATC vet code amended)
•
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 , and
Trichostrongylus species in sheep in a number of countries, including the EU.
There are reports of resistance in in sheep outside the EU.
Resistance to levamisole has been reported in
in developed countries such as 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.
In cases of lungworm infections, coughing may persist for a considerable time
following successful treatment due to tissue damage caused by the parasite.
i. Special precautions for use in animals
Care should be taken to estimate accurately the liveweight of animals to
be treated. After treatment animals should be moved to clean pasture in
order to prevent re-infection.
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 might be
involved.
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Do not eat, drink or smoke when using this product. Care should be taken
to avoid accidental self-injection: may cause irritation at site of injection.
Wash splashes from eyes and skin immediately. If irritation persist, seek
medical advice. Remove any contaminated clothing immediately. Wash
hands and exposed skin after handling this product and before meals.
Levamisole can cause idiosyncratic reactions and serious blood disorders
in a very small number of people. If symptoms such as dizziness,
nausea, vomiting or abdominal discomfort are experienced when using
Revised: July 2010
(ATC vet code amended)
this product, or sore mouth, throat or fever occur shortly afterwards, then
medical advice should be sought immediately.
Protect from light.
In order to minimise the risk of infection, needles should be changed as
frequently as possible.
Following withdrawal of the first dose, use the product within 28 days.
last treatment. Sheep may be slaughtered for human consumption only after
15 days from the last treatment.
This product must not be used in cattle and sheep producing milk for human
consumption.
Revised: July 2010
(ATC vet code amended)
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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Other Products Containing Levamisole Hydrochloride
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Chanaverm 7.5% Oral Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Chanaverm 7.5% Oral Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep
POM-VPSElanco GmbH
Combinex 50 mg/ml + 37.5 mg/ml Oral Suspension for Sheep
POM-VPSElanco GmbH
Combinex Cattle Oral Suspension
POM-VPSElanco Europe Ltd
Downland Fluke and Worm Oral Suspension
POM-VPSNorbrook Laboratories Limited
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