NOAH Compendium

Printed from NOAH Compendium (https://www.noahcompendium.co.uk). (c) Copyright NOAH Compendium 2024. All Rights Reserved.
Date: Saturday, June 15, 2024 1:11

Release 2.138
Solantel 50 mg/ml Oral Suspension for Sheep
 
Species: Sheep
Therapeutic indication: Pharmaceuticals: Endoparasiticides: Anthelmintics for sheep, Flukicides, Combination fluke/wormers
Active ingredient: Closantel
Product:Solantel 50 mg/ml Oral Suspension for Sheep
Product index: Solantel Drench
Sheep - meat: 42 days
Withdrawal notes: Sheep: Not authorised for use in ewes producing milk for human consumption incl dry period. Do not use within 1 year prior to the first lambing in ewes intended to produce milk for human consumption.
Incorporating:
Qualitative and quantitative composition
One ml contains:
Active substance(s):
Closantel
50.0 mg
(as Closantel Sodium Dihydrate)
54.375mg
Excipients:
Propylene glycol (E1520)
217.6 mg
For a full list of excipients, see section Pharmaceutical Particulars
Pharmaceutical form
Oral suspension.
Off-white to yellow suspension.
Clinical particulars
Target species
Sheep
Indications for use, specifying the target species
For the treatment of chronic and subacute fasciolosis (due to Fasciola hepatica). The product is effective against mature and late immature flukes (from 5 weeks immature).
For the treatment of Oestrus ovis (Sheep Nasal Bot Fly).
For the treatment of inhibited, L4 and adult stages of Haemonchus contortus.
Contraindications
Do not use in animals with known hypersensitivity to the active substance or to any of the excipients.
Special warnings for target species
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, 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 closantel has been reported in Haemonchus species outside the EU. 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.
Special precautions for use
i. Special precautions for use in animals
When using a drenching gun, take care not to injure the mouth or pharynx.
Do not exceed the stated dose.
The product can be used in all age groups of sheep and lambs.
ii. Special precautions to be taken by the person administering the veterinary medicinal product to animals
This product may be irritating to skin and eyes and users should be careful not to accidentally splash it on themselves or others.
Wear nitrile rubber gloves when applying the product.
In case of accidental spillage onto skin or into eyes, rinse the affected area with large amounts of clean water. If irritation persists, seek medical advice immediately and show the package leaflet or label to the physician.
Wash hands after use.
Do not eat, drink or smoke while handling the product.
iii. Other precautions
Closantel is very toxic to dung fauna.
The risk to dung fauna can be reduced by avoiding too frequent and repeated use of closantel (and products of the same anthelmintic class) in sheep and lambs. Animals should not normally be treated in excess of three times a year with closantel.
Adverse reactions (frequency and seriousness)
None known.
Use during pregnancy, lactation or lay
The product can be used at any time during pregnancy. It can also be used in rams at any time including during the breeding season. The safety of the product for use during lactation has not been established.
Interaction with other medicinal products and other forms of interaction
None known.
Amounts to be administered and administration route
Give orally as a drench.
10 mg of closantel per kg bodyweight (i.e. 1 ml of product per 5 kg bodyweight).
For example:
Bodyweight
Dose
Up to 5 kg
1 ml
10 kg
2 ml
20 kg
4 ml
30 kg
6 ml
40 kg
8 ml
50 kg
10 ml
60 kg
12 ml
70 kg
14 ml
80 kg
16 ml
To ensure administration of a correct dose, bodyweight 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 body weight and dosed accordingly in order to avoid under- or over-dosing.
The timing for treatment should be based on epidemiological factors and should be customised for each individual farm. As with other anthelmintics, veterinary advice should be sought on appropriate dosing programmes and stock management to achieve adequate parasite control and reduce the likelihood of resistance developing.
Suitable for use with most types of standard drenching equipment.
Shake well before use.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Symptoms of acute overdosage are decreased vision or blindness, anorexia, in-coordination and general weakness.
Withdrawal period(s)
Meat and offal: 42 days
Not authorised for use in ewes producing milk for human consumption including during the dry period. Do not use within 1 year prior to the first lambing in ewes intended to produce milk for human consumption.
Pharmacological particulars
Pharmacotherapeutic group: Anthelmintics, phenol derivatives, including salicylanilides.
ATC Vet Code: QP52AG09
Pharmacodynamic properties
The product contains the salicylanilide closantel, a synthetic antiparasitic agent with high activity against liver fluke, haematophagous nematodes and the larval stages of some arthropods in sheep.
Closantel uncouples the mitochondrial oxidative phosphorylation resulting in inhibition of ATP synthesis. This induces a marked change in the energy metabolism of the parasite which finally kills it.
Closantel is active against benzimidazole resistant strains of Haemonchus contortus.
Pharmacokinetic particulars
Closantel is rapidly absorbed into the systemic circulation with peak plasma levels at 24-48 hours after dosing. The bioavailability of an oral dose is 50 %. In plasma, closantel is bound to albumin for more than 99 %. As a result, tissue distribution is very limited. On average, tissue levels are 15 times lower than plasma levels. The elimination half-life of closantel from plasma and tissues is approximately 2 to 4 weeks in sheep. Closantel is metabolised only to a slight extent and the main excretion route is the bile. The urinary excretion is negligible.
Environmental properties
Closantel has the potential to adversely affect non-target organisms. Following treatment, excretion of potentially toxic levels of closantel may take place over a period of several weeks. Faeces containing closantel excreted onto pasture by treated animals may reduce the abundance of dung feeding organisms which may impact on the dung degradation.
Pharmaceutical particulars
List of excipients
Propylene Glycol (E1520)
Microcrystalline Cellulose and Carmellose Sodium
Hypromellose
Sodium Lauryl Sulfate
Simethicone Emulsion
Water purified
Incompatibilities
In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years
Shelf-life after first opening the immediate packaging: 28 days.
Special precautions for storage
Do not store above 30 °C.
Keep the container in the outer carton in order to protect from light.
Store upright in the original container.
Protect from cold and shake well before use.
Nature and composition of immediate packaging
White high density polyethylene multidose container backpacks with high density polyethylene screw cap with induction-seal liners.
Pack sizes:
Box with 1 multidose container of 1 litre
Box with 1 multidose container of 2.5 litres
Box with 1 multidose container of 5 litres
Not all pack sizes may be marketed.
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products
Closantel may affect aquatic organisms. Do not contaminate ponds, waterways or ditches with the product or empty containers.
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
Marketing Authorisation Holder (if different from distributor)
Norbrook Laboratories Limited, Station Works, Camlough Road, Newry, Co. Down, BT35 6JP Northern Ireland
Marketing Authorisation Number
Vm 02000/4402
Significant changes
Date of the first authorisation or date of renewal
04 August 2016
Date of revision of the text
August 2021
Any other information
Nil.
Legal category
Legal category: POM-VPS
GTIN
GTIN description:Solantel 50mg/ml Oral Suspension for Sheep - 1 Litre
GTIN:5023534028420
GTIN description:Solantel 50mg/ml Oral Suspension for Sheep - 2.5 Litre
GTIN:5023534028437
GTIN description:Solantel 50mg/ml Oral Suspension for Sheep - 5 Litre
GTIN:5023534028444