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AN: 01458/2012
Revised April 2013
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Quiflox 20 mg/ml solution for injection for cattle (calves) and pigs
Marfloquin 20 mg/ml solution for injection for cattle (calves) and pigs
Quiflox 20 mg/ml solution for injection for cattle (calves) and pigs (Czech
Republic, Hungary, Latvia, Lithuania, Slovak Republic)
Marfloquin 20 mg/ml solution for injection for cattle (calves) and pigs (Austria,
Belgium, Denmark, Finland, France, Germany, Greece, Italy, Luxembourg,
Netherlands, Norway, Portugal, Spain, United Kingdom)
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 ml of solution for injection contains:
Active substance:
Marbofloxacin 20 mg
Excipients:
Metacresol
Disodium edetate
Monothioglycerol
2 mg
0.10 mg
0.50 mg
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection.
Clear, greenish yellow to brownish yellow solution.
4.
CLINICAL PARTICULARS
4.1 Target species
Cattle (calves).
Pigs.
4.2 Indications for use, specifying the target species
In pre-ruminant and ruminant calves:
- treatment of respiratory infections caused by sensitive strains of Pasteurella
multocida, Mannheimia haemolytica, and Mycoplasma bovis.
In pigs:
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- treatment of respiratory infections caused by sensitive strains of Actinobacillus
pleuropneumoniae, Mycoplasma hyopneumoniae, and Pasteurella
multocida.
This product should only be used based on susceptibility testing.
4.3 Contraindications
Do not use in case of disturbance in growth of cartilage and/or during injury of
locomotion system particulary on functionally loaded joints.
Do not administer in animals with known hypersensitivity to marbofloxacin or
any other quinolone or to any of the excipients.
4.4 Special warnings for each target species
None.
4.5 Special precautions for use
i.
Special precautions for use in animals
Official and local antimicrobial policies should be taken into account
when the product is used.
Fluoroquinolone should be reserved for the treatment of clinical
conditions which have responded poorly, or are expected to respond
poorly, to other classes of antimicrobials.
Where possible, fluoroquinolones should be used based on
susceptibility testing.
Use of the product deviating from instructions given in the SPC may
increase the prevalence of bacteria resistant to fluoroquinolones and
may decrease the effectiveness of treatment with other quinolones due
to the potential for cross resistance.
ii.
Special precautions to be taken by the person administering the
veterinary medicinal product to animals
Wash hands after use.
People with known hypersensitivity to (fluoro)quinolones should avoid
contact with the product.
Direct contact with skin should be avoided to reduce the risk of
sensitisation and contact dermatitis.
In case of contact with skin or eyes, rinse with plenty of water.
Care should be taken to avoid accidental self injection.
In case of accidental self injection, seek a medical advice and show the
label to the doctor.
Accidental self-injection can induce a slight irritation.
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4.6 Adverse reactions (frequency and seriousness)
Administration by the subcutaneous route may induce a transient oedema.
Intramuscular administration may cause pain and inflammatory lesions at the
injection site. The inflammatory lesions persist 6 days in pigs and 12 days in
calves.
4.7 Use during pregnancy, lactation or lay
Studies in laboratory animals (rats, rabbits) did not show any evidence of a
teratogenic, embryotoxic or maternotoxic effect associated with the use of
marbofloxacin.
The product should be used according to the benefit/risk assessment carried
out by the veterinarian.
See section 4.11 for withdrawal periods.
4.8 Interaction with other medicinal products and other forms of interaction
None known.
4.9 Amounts to be administered and administration route
Pre-ruminant and ruminant calves:
- Intramuscular or subcutaneous use:
2 mg of marbofloxacin per kg of bodyweight per day, i.e. 1 ml of solution per 10
kg of body weight in a single daily injection for 3 to 5 days. The first injection
may also be given by the intravenous route.
Pigs:
- Intramuscular use:
2 mg of marbofloxacin per kg of body weight per day, i.e.1 ml of solution per 10
kg of body weight in a single daily injection for 3 to 5 days.
The dose volume given at one injection site should not exceed 6 ml in calves
and 3 ml in pigs.
As the vial cannot be broached more than 20 times, the user should choose the
most appropriate vial size according to the target species to treat.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
No sign of overdosage has been observed with marbofloxacin after
administration of 3 times the recommended dose.
Overdosage symptoms of marbofloxacin are acute neurological disorders that
should be treated symptomatically.
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4.11
Withdrawal period(s)
Meat and offal:
-pre-ruminant and ruminant calves: 6 days.
-pigs: 4 days.
This product is not authorised for use in lactating animals producing milk for
human consumption.
5.
PHARMACOLOGICAL PROPERTIES
Pharmacotherapeutic group: Antibacterials for systemic use, Fluoroquinolones,
ATCvet code: QJ01MA93
5.1 Pharmacodynamic properties
Marbofloxacin is a synthetic, bactericidal antimicrobial belonging to the
fluoroquinolone group. It acts by inhibition of DNA gyrase and has a broadspectrum activity against Gram-positive bacteria (especially Staphylococcus),
and Gram-negative bacteria (Escherichia coli, Pasteurella multocida,
Mannheimia haemolytica and Actinobacillus pleuropneumoniae, as well as
against mycoplasma (Mycoplasma bovis and Mycoplasma hyopneumoniae).
Cases of resistance have been observed in Streptococcus.
Strains with MIC ≤ 1 µg/ml are sensitive to marbofloxacin whereas strains with
MIC ≥ 4 µg/ml are resistant to marbofloxacin.
Resistance to fluoroquinolones occurs by chromosomal mutation with three
mechanisms: decrease of the bacterial wall permeability, expression of efflux
pump or mutation of enzymes responsible for molecule binding.
5.2 Pharmacokinetic particulars
Following subcutaneous or intramuscular administration of the recommended
dose of 2 mg/kg in cattle or pigs, marbofloxacin is rapidly absorbed and attains
its maximum plasma concentration of 1.5 µg/ml within less than an hour. Its
bioavailability is close to 100%.
Marbofloxacin is weakly bound to plasma proteins (< 10% in pigs, < 30% in
cattle) and widely distributed throughout the organism. In the majority of tissues
(liver, kidney, skin, lung, uterus), it achieves a higher concentration than in
plasma.
Marbofloxacin is eliminated slowly in pre-ruminating calves (t½β = 5-9 h) and in
pigs (t½β = 8-10 h), but faster in ruminant cattle (t½β = 4-7 h) predominantly in
the active form in urine and faeces.
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6.
PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Gluconolactone
Disodium edetate
Mannitol
Metacresol
Monothioglycerol
Water for injections
6.2 Incompatibilities
Do not mix with other medicinal products.
6.3 Shelf life
Shelf-life of the veterinary medicinal product as packaged for sale: 3 years.
Shelf-life after first opening the immediate packaging: 28 days.
6.4. Special precautions for storage
Store in the original package in order to protect from light.
Do not freeze.
6.5 Nature and composition of immediate packaging
Bottle (amber glass Ph. Eur. type II), bromobutyl rubber stopper, aluminium
closure: 50 ml solution for injection, in a box.
Bottle (amber glass Ph. Eur. type II), bromobutyl rubber stopper, aluminium
closure: 100 ml solution for injection, in a box.
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 product or waste material should be disposed of in accordance with
national requirements.
7.
MARKETING AUTHORISATION HOLDER
Krka Dd
Novo Mesto
Šmarješka Cesta 6
Novo Mesto
8501
Slovenia
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8.
MARKETING AUTHORISATION NUMBER
Vm 01656/4025
9.
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date: 06 September 2011
10. DATE OF REVISION OF THE TEXT
Date: April 2013
PROHIBITION OF SALE, SUPPLY AND/OR USE
Veterinary prescription.
APPROVED 12/04/13
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