Kefavet Vet.
SUMMARY OF PRODUCT CHARACTERISTICS
1. NAME OF THE VETERINARY MEDICINAL PRODUCT
KEFAVET vet. 250 mg film-coated tablets
KEFAVET vet. 500 mg film-coated tablets
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Active substance:
Kefavet vet. 250 mg film-coated tablets
Cefalexin monohydrate equivalent to 250 mg anhydrous cefalexin
Kefavet vet. 500 mg film-coated tablets
Cefalexin monohydrate equivalent to 500 mg anhydrous cefalexin
Excipients:
Kefavet vet. 250 mg film-coated tablets
Titanium dioxide E171 0.550 mg
Kefavet vet. 500 mg film-coatedtablets
Titanium dioxide E171 1.10 mg
For the full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Film-coated tablet.
250 mg: White to yellowish,
round (diameter approx. 10 mm), biconvex tablet scored on one side,
“CX” above the score, “250” below the score.
500 mg: White to yellowish, oblong (size approx. 7 x 18 mm), biconvex tablet scored on both sides.
4. CLINICAL PARTICULARS
4.1 Target species
Dog
4.2 Indications for use, specifying the target species
Treatment of urinary tract infections and recurring severe dermatological infections caused by bacteria sensitive to cefalexin.
4.3 Contraindications
Do not use in case of hypersensitivity to the cephalosporins or penicillin or to any of the excipients.
Do not use in case of resistance to the cephalosporins or penicillins occur.
Do not use in rabbits, guinea pigs, hamsters and gerbils.
4.4 Special warnings for each target species
None.
4.5 Special precautions for use
Special precautions for use in animals
In cases of known renal insufficiency, the dose must be reduced. Use of the product should be based on susceptibility testing and it should take into account official and local antimicrobial policies.
Inappropriate use of the product may increase the prevalence of bacteria resistant to cefalexin and may decrease the effectiviness of treatment with other beta-lactam antibiotics, due to the potential for cross resistance.
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 penicillin may lead to cross-reactions to cephalosporin and vice versa. Allergic reactions to these substances may occasionally be serious.
Do not handle this veterinary medicinal product if you know you are sensitised or if you have been advised not to be in contact with such substances.
Handle this veterinary medicinal 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 package leaflet or the label to the physician. Swelling of the face, lips or eyes or difficulty breathing, are more serious symptoms and require urgent medical attention.
In case of accidental ingestion, especially by a small child, seek medical advice immediately and show the package leaflet or the label to the physician.
4.6 Adverse reactions (frequency and seriousness)
Diarrhoea and vomiting, most often mild, can occur. In the event of severe gastrointestinal side effects, treatment should be discontinued.
4.7 Use during pregnancy, lactation or lay
The safety of the veterinary medicinal product has not been established during pregnancy and lactation.
Use only accordingly to the benefit/risk assessment by the responsible veterinarian.
4.8 Interaction with other medicinal products and other forms of interaction
Due to undesirable pharmacodynamicinteraction, do not apply cefalexinsimultaneously with pharmaceuticals acting bacteriostatically.
In order to ensure efficacy, the veterinary medicinal product should not be used in combination with bacteriostatic antibiotics.
Concurrent use of first generation cephalosporins with aminoglycoside antibiotics or some diuretics such as furosemide can enhance nephrotoxicity risks.
4.9 Amounts to be administered and administration route
For oral administration
For urinary tract infections: 15 mg/kg body weight twice daily for 14 days.
For recurring severe dermatological infections: 25-30 mg/kg twice daily for at least three weeks. Treatment times of 4-6 weeks may be required for deep pyoderma. It is recommended to assess the benefit/risk and the duration of treatment after one month by the responsible veterinarian. To ensure a correct dosage body weight should be determined as accurately as possible to avoid underdosing.
Kefavet vet. tablets can be crushed or added to food, if necessary.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
The acute symptom of cefalexin toxicity following an oral dose of 500 mg/kg has been shown to be vomiting. Salivating and individual emetic responses have been observed after oral doses of 200 and 400 mg/kg cefalexin over 365 days.
4.11 Withdrawal period
Not applicable.
5. PHARMACOLOGICAL PROPERTIES
Pharmacotherapeutic group: Other beta-lactam antibacterials,First-generation cephalosporines
ATCvet code: QJ01DB01
5.1 Pharmacodynamic properties
Cefalexin is a beta-lactam antibiotic in the first-generation cephalosporins. It inhibits bacterial cell membrane synthesis in a similar way to penicillin. Cephalosporins reduce the build-up of bacterial cell membranes, which leads to abnormal elongation of cells, formation of spheroplasts or osmotic lysis. In general, cephalosporins are bactericidal in effect. The bactericidal effect of cefalexin is mainly time dependent.
Antibacterial spectrum
Cefalexin is effective against Gram-positive cocci, including penicillinase-producing staphylococci, Gram-positive rods and Gram-negative bacteria, e.g. E.coli. Indole-positive Proteus species, excluding P. Mirabilis, are often resistant to cefalexin, as are certain Enterobacteria and Bacteroides species. Methicillin-resistant staphylococci are also generally resistant to cephalosporins, as are all enterococci and Pseudomonas aeruginosa.
Cephalosporins are however resistant in varying degrees to beta-lactamase produced by staphylococci and Gram-negative bacteria. Staphylococci sensitive to methicillin or oxacillin can be regarded as being sensitive to oral cephalosporins regardless of penicillinase production.
Development of resistance is mainly based on the formation of beta-lactamase, an enzyme that breaks open the beta-lactam ring, rendering the antibiotic ineffective. Cross resistance exists between antibiotics belonging to the beta-lactam group.
5.2 Pharmacokinetic particulars
Peak plasma concentration (Cmax) is between 19-32 microgram/ml, the time until Cmax is achieved (Tmax) is then 1-2 hours and the elimination half-life (t1/2) is 1.7-2.8 hours when 25 mg cefalexin/kg body weight is administered orally to dogs.
The bioavailability of cefalexin is approx. 75% following oral administration.
A small proportion (18%) of cefalexin is bound to serum proteins in dogs.
Following a dose of 200 mg/kg, a low concentration of cefalexin activity was apparent in the brain, while no activity was apparent in the brain following a dose of 25 mg/kg. Cmax in skin 2 hours after oral administration of 25 mg/kg cefalexin has been shown to be 7.3-10.8 microgram/g (20-40% of the plasma concentration). After 12 hours, the concentration had dropped to 1.4-1.7 microgram/g. The cefalexin concentration in kidneys is approximately quadruple the concentration in the blood.
Renal excretion is the main elimination path for cefalexin in dogs. Tubular secretion of cefalexin through the kidneys is dependent on the concentration of free cefalexin in the blood. Approximately 40% of an oral dose is excreted unaltered 24 hours after dose administration. Renal clearance of cefalexin is approximately 55-63 ml/min m2 body surface.
6. PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Macrogol
Magnesium stearate
Sodium starch glycolate (type A)
Povidone
Lactose monohydrate
Saccharin sodium
Peppermint oil
Titanium dioxide (E171)
Talc
Hypromellose
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 3 years.
6.4. Special precautions for storage
Store below 25 C in the original package. Protect from light and moisture.
6.5 Nature and composition of immediate packaging
PVC/PVDC/Al blister.
250 mg: 14, 20, 28, 70 and 140 tablets
500 mg: 14, 28, 30, 70 and 140 tablets
Not all pack sizes may be marketed.
6.6 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.
7. MARKETING AUTHORISATION HOLDER
To be completed nationally.
8. MARKETING AUTHORISATION NUMBER(S)
To be completed nationally
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
To be completed nationally.
10 DATE OF REVISION OF THE TEXT
18 July 2014
PROHIBITION OF SALE, SUPPLY AND/OR USE
Not applicable.
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