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Date: Wednesday, April 24, 2024 9:57

Description: Ceva logo
Release 3.61
Therios® 75 mg Chewable Tablets for Cats
 
Species: Cats
Therapeutic indication: Pharmaceuticals: Antimicrobials: Oral preparations: Tablets
Active ingredient: Cefalexin
Product:Therios® 75 mg Chewable Tablets for Cats
Product index: Therios 75 mg Tablets for Cats
Incorporating:
Qualitative and quantitative composition
Each tablet contains
Active substance:
Cefalexin (as cefalexin monohydrate) 75 mg
Excipients:
For the full list of excipients, see Pharmaceutical particulars.
Pharmaceutical form
Chewable tablet. Oblong scored beige tablet. The tablets can be divided into equal halves
Clinical particulars
Target species
Cats
Indications for use
Infections caused by bacteria susceptible to cefalexin. Lower urinary tract infections due to E.coli and Proteus mirabilis.
Treatment of cutaneous and subcutaneous infections: pyoderma due to Staphylococcus spp. and wounds and abscesses due to Pasteurella spp.
Contraindications
Do not use in case of severe kidney failure
Do not use in animals which are known to be hypersensitive to cephalosporins or any other substance from the β-lactam group.
Do not use in rabbits, guinea pigs, hamsters and gerbils and other small rodents.
Special warnings for each target species
None
Special precautions for use
Special precautions for use in animals
As with other antibiotics which are excreted mainly by the kidneys, systemic accumulation may occur in the body when renal function is impaired. In cases of known renal insufficiency, the dose should be reduced and/or the interval of administration increased and nephrotoxic drugs should not be administered concurrently.
Wherever possible, the use of the product should be based on susceptibility testing.
Official and local antimicrobial policies on antibiotherapy should be taken into account when the product is used.
Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to the cefalexin and may decrease the effectiveness of treatment with penicillins due to the potential for cross resistance.
This product should not be used to treat kittens less than 9 weeks of age.
Use of the product in cats weighing less than 2.5 kg should be in accordance with the benefit/risk assessment performed by the responsible veterinarian. The chewable tablets are flavoured. In order to avoid any accidental ingestion, store tablets out of reach of the animals.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross-reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.
Do not handle this product if you know you are sensitised, or if you have been advised not to be in contact with such substances.
Handle this product with great care to avoid exposure taking all recommended precautions. Wash hands after use.
If you develop symptoms following exposure, such as skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty in breathing are more serious symptoms and require urgent medical attention.
In case of accidental ingestion, seek medical attention and show the package leaflet or the label to the doctor.
Adverse reactions
Vomiting and/or diarrhoea have been observed.
Allergic reactions are possible with cefalexin and allergic cross-reactivity with other β-lactams may occur.
Use during pregnancy or lactation
Laboratory studies in mouse, rat and rabbit have not produced any evidence of teratogenic effects. The safety of the product has not been investigated in pregnant or lactating cats and should only be used according to the benefit/risk assessment by the responsible veterinarian.
Interaction with other medicinal products and other forms of interaction
The bactericidal activity of cephalosporins is reduced by concomitant administration of bacteriostatic acting compounds (macrolides, sulfonamides and tetracyclines).
Nephrotoxicity can be increased when 1st generation cephalosporins are combined with polypeptide antibiotics, aminoglycosides or some diuretics (furosemide).
Concomitant use with such active substances should be avoided.
Amounts to be administered and administration route
Oral use.
15 mg cefalexin per kg bodyweight twice daily, equivalent to 1 tablet for 5 kg bodyweight for:
- 5 days for wounds and abscesses
- 10 to 14 days in case of urinary tract infections
- 14 days at least in case of pyoderma. The treatment must be continued for 10 days once the lesions have disappeared.
To ensure a correct dosage bodyweight should be determined as accurately as possible to avoid underdosing
In case of use of half tablets, put the remaining quantity of the tablet back into the blister pocket and use it for the next administration.
The tablets are flavoured. They can be administered with food or directly into the mouth of the animal.
Overdose (symptoms, emergency procedures, antidotes), if necessary
Not applicable
Withdrawal period(s)
Not applicable
Pharmacological particulars
Pharmacotherapeutic group: Antibacterial for systemic use, first-generation cephalosporin. ATCvet code: QJ01DB01
Pharmacodynamic properties
Cefalexin monohydrate is a bactericidal antibiotic of the cephalosporin family, obtained by hemi-synthesis of the 7-amino cephalosporanic nucleus.
Cefalexin acts by inhibiting the nucleopeptide synthesis of the bacterial wall. Cephalosporins interfere with transpeptidation by acylating the enzyme making it unable to cross-link muramic acid-containing peptidoglycan strands. The inhibition of the biosynthesis of the material required to build the cell wall results in a defective cell wall and consequently osmotically unstable to protoplasts. The combined action results in cell lysis and filament formation. Cefalexin is active against Gram positive and Gram negative bacteria such as Staphylococcus spp. (including penicillin-resistant strains), Streptococcus spp.,and Escherichia coli. Cefalexin is not inactivated by β-lactamases produced by Gram positive bacteria. However, beta-lactamases produced by Gram-negative bacteria can inhibit cefalexin by hydrolysis of the beta-lactam cycle.
Resistance to cefalexin may be due to one of the following mechanisms of resistance. Firstly, the production of various beta-lactamases (cephalosporinase), that inactivate the antibiotic, is the most prevalent mechanism among Gram-negative bacteria. Secondly, a decreased affinity of the PBPs (penicillin-binding proteins) for beta-lactam drugs is frequently involved for beta-lactam resistant Gram-positive bacteria. Lastly, efflux pumps, extruding the antibiotic from the bacterial cell, and structural changes in porins, reducing passive diffusion of the drug through the cell wall, may contribute to improve the resistant phenotype of a bacterium.
Well-known cross-resistance (involving the same resistance mechanism) exists between antibiotics belonging to the beta-lactam group due to structural similarities. It occurs with β-lactamase enzymes, structural changes in porins or variations in efflux pumps. Co-resistance (different resistance mechanisms involved) has been described in E.coli due to a plasmid harbouring various resistance genes.
MICs parameters available for Staphylococcus spp. and Pasteurella multocida are:
Staphylococcus spp MIC 50 2 µg/ml MIC90 2 µg/ml
Pasteurella multocida MIC 50 2 µg/ml MIC90 4 µg/ml
Pharmacokinetic properties
In cats, the bioavailability after oral administration is around 56%.
In cats, after a single oral administration of 18.5 mg/kg of cefalexin, the plasmatic peak was reached after 1.6 h with a concentration of 22 µg/ml.
Cefalexin was detected in plasma till 24 hours after administration.
The diffusion of cefalexin in tissue is high. Cefalexin is mainly eliminated by urinary route (85%) under active form, urinary concentration peaks are significantly higher than plasmatic concentration peaks.
Pharmaceutical particulars
Excipients
Pig liver powder, Yeast, Croscarmellose sodium, Magnesium stearate, Anhydrous colloidal silica, Calcium hydrogen phosphate dihydrate.
Incompatibilities
Not applicable
Shelf life
Shelf-life of the veterinary medicinal product as packaged for sale:
Polyvinylchloride / thermo-elast / polyvinylidene chloride – aluminium heat sealed blister: 3 years
Polyamide / aluminium / polyvinylchloride – aluminium heat sealed blister: 30 months
Any divided tablet portions remaining after 24 hours should be discarded
Special precautions for storage
Do not store above 25°C. Store in the original package. Return any halved tablet to the opened blister pack.
Nature and composition of immediate packaging
Blister:
Polyvinylchloride / thermo-elast / polyvinylidene chloride – aluminium heat sealed containing 10 tablets per blister
Polyamide / aluminium / polyvinylchloride – aluminium heat sealed containing 10 tablets per blister
Cardboard box with 1 blister of 10 tablets; Cardboard box with 2 blisters of 10 tablets; Cardboard box with 10 blisters of 10 tablets; Cardboard box with 15 blisters of 10 tablets; Cardboard box with 20 blisters of 10 tablets.
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
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
Marketing Authorisation Number
UK: Vm 15052/4118
Significant changes
Date of the first authorisation or date of renewal
6 October 2010
Date of revision of the text
October 2022
Any other information
Nil
Legal category
Legal category: POM-V
GTIN
GTIN description:Therios 75 mg 20x10T
GTIN:03411112276141