Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole)
Fenbendazole
Last verified
Veterinary medicinal product: granules. Distribution category: AVM-GSL (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Fenbendazole.1
In short: questions and answers
- Does Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) need a prescription?
- Over the counter. As stated in the registration decision.1
- Which animals is Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) for?
- Dogs.1
- What is the active substance in Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole)?
- Fenbendazole. ATCvet code: QP52AC13.13
- What is the withdrawal period of Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole) according to the leaflet?
- No withdrawal period is set for this drug: it is not intended for food-producing animals.3
- Dispensing
- Over the counter1
AVM-GSL: Authorised Veterinary Medicine - General Sale List. No prescription is needed and it may be sold by any retailer.12
Supplied without a prescription. As stated in the registration decision.
- Animal species
- Dogs1
- Active substance
- Fenbendazole
- ATCvet code
- QP52AC133
- Manufacturer
- Marketing authorisation holder: C&H Generics Ltd
Withdrawal period
No withdrawal period is set for this drug: it is not intended for food-producing animals.3
Summary of product characteristics
Composition
Each sachet contains:
Active substance:
Fenbendazole 888.8 mg
Excipient(s):
For the full list of excipients, see section 6.1.
6.1 List of excipients
Lactose monohydrate
Povidone
Sodium laurilsulfate
Pharmaceutical form
Granules
A free flowing white to greyish white granular powder
Pharmacological properties
Anthelminthics (Benzimidazoles and related substances) ATC code: QP52AC13
5.1 Pharmacodynamic properties
Contains fenbendazole which is a member of the benzimidazole family of anthelmintics and has been in veterinary use for a number of years. It acts against parasites by disrupting the formation of microtubules by binding to tubulin in parasitic intestinal cells hence preventing the absorption of glucose, and as a result the parasites are gradually starved to death. Fenbendazole displays preference for parasitic as opposed to mammalian tubulin; this appears to be due to the fact that the formation of the parasitic tubulin-fenbendazole complex is more favourable kinetically under physiological conditions than the mammalian complex.
5.2 Pharmacokinetic particulars
Fenbendazole is only partly absorbed from the intestine and reaches maximum plasma concentration in dogs 4 - 9 hours after oral administration.
Fenbendazole and its metabolites are distributed throughout the body but highest concentrations are found in the liver.
Fenbendazole is metabolised mainly by enzymes of the cytochrome P-450 system in the liver. The major oxidative metabolite is fenbendazole sulfoxide which is further metabolised to fenbendazole sulfone.
Fenbendazole and its metabolites are predominantly excreted via the faeces.
Target species
Dogs.
Indications
Dogs
For the treatment of immature and mature stages of Toxacara canis and Taenia hydatigena.
Dosage
For oral administration only; sprinkled onto food.
For the routine treatment of adult dogs a dosage of 100 mg/kg is recommended. This equates to approximately 1 whole sachet per 8 kg bodyweight (2 sachets for 16 kg bodyweight; 3 sachets for 24 kg bodyweight etc.).
Sachets must not be divided and stored for future use. If necessary, a suitable alternative product must be selected.
To ensure administration of a correct dose, body weight should be determined as accurately as possible.
Contraindications
Do not use in cases of hypersensitivity to the active substance, or to any of the excipients.
Adverse reactions
None known
Warnings
Special precautions for use in animals
Not applicable
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Embryotic effects cannot be excluded. Pregnant women must take extra precautions when handling this product.
This product may be toxic to humans after ingestion. Accidental ingestion of the product should be avoided. In the event of accidental ingestion, rinse mouth with plenty of clean water and seek medical advice.
The product can cause irritation to the skin, eyes and lungs. Avoid contact with skin and/or eyes. Avoid inhalation of granule dust. When handling and applying to food, care should be taken to avoid direct contact with the skin and eyes and inhalation of dust. Wash hands after use. In case of accidental skin and/or eye contact, immediately rinse with plenty of clean water. If irritation persists, seek medical advice. Only use for the bodyweight of animal recommended. The entire contents of the sachet must be directly sprinkled onto food as a single dose. Discard any uneaten medicated feed immediately.
Use during pregnancy, lactation or lay
The use is not recommended during pregnancy or lactation.
Use only according to the benefit/risk assessment by the responsible veterinarian.
Interactions
None known.
Overdose
Benzimidazoles have a wide margin of safety.
Special warnings
None
Withdrawal period
Not applicable.
Incompatibilities
In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
Immediate packaging
Sachet consisting of paper, low density polyethylene and foil containing 4g of granules, with a heat-seal closure.
Each carton contains 1, 2, 3, 4 or 5 sachets.
Not all pack sizes may be marketed.
Storage
Store in a dry place.
Add to feed immediately before administration. Discard any remaining medicated feed.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 3 years.
Disposal of unused product
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements
Additional information
Vm 40162/4006
9 DATE OF FIRST AUTHORISATION
02 December 2016
10 DATE OF REVISION OF THE TEXT
January 2022
Approved 10 January 2022
Registration holder
C&H Generics Ltd c/o Michael McEvoy and Co.
Seville House
New Dock Street
Galway
Ireland
Regulations
- Veterinary Medicines Regulations 2013 (SI 2013/2033), Schedule 32
Sources
- VMD Product Information Database: Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole), 40162/4006
- The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products)
- Summary of Product Characteristics: Ridaworm Wormer Granules 888 mg for Adult Dogs (Fenbendazole)
Other products with the same active substance
- Curofen 50 mg/g Oral Powder for Pigs
- Curofen 50 mg/g Premix for Medicated Feeding Stuff for Pigs
- Ecozole 4% w/w Premix for Medicated Feeding Stuff
- Gallifen 40 mg/g Premix for Medicated Feeding Stuff for Chickens and Pheasants
- Johnson's Veterinary Easy Round Wormer Granules for Cats & Kittens 222.2 mg
- Meranox 25 mg/ml Oral Suspension for Pigeons
- Panacur 10% Oral Suspension
- Panacur 187.5 mg/g Oral Paste for Dogs and Cats
- Panacur AquaSol 200 mg/ml Oral Suspension for Use in Drinking Water for Pigs and Chicken
- Panacur Granules 222 mg/g
- Panacur Small Animal 100 mg/ml Oral Suspension
- Parazole Dog/Cat 100 mg/ml Oral Suspension
All products with this active substance (17)
The same active substance in other countries
Spain
- CUROFEN 50 mg/g POLVO ORAL PARA PORCINO
- GALLIFEN 40 mg/g PREMEZCLA MEDICAMENTOSA PARA POLLOS Y FAISANES
- PANACUR 250 mg COMPRIMIDOS PARA PERROS Y GATOS
- PANACUR 500 mg COMPRIMIDOS PARA PERROS
- PIGFEN 200 mg/ml SUSPENSION PARA ADMINISTRACION EN AGUA DE BEBIDA PARA PORCINO
All products with this active substance (7)
Poland
- Fenbenat
- Helmigal 40 mg/g proszek doustny dla świń i dzików
- Panacur Tabletki 250 mg dla psów i kotów
- Pigfen 40 mg/g premiks do sporządzania paszy leczniczej dla świń
All products with this active substance (4)