NUFLOR VETERINARY

देश: इसराइल

भाषा: अंग्रेज़ी

स्रोत: Ministry of Health

सक्रिय संघटक:

FLORFENICOL

थमां उपलब्ध:

INTERVET ( ISRAEL) LTD

फार्मास्यूटिकल फॉर्म:

SOLUTION FOR INJECTION

रचना:

FLORFENICOL 300 MG/ML

प्रशासन का मार्ग:

I.M

प्रिस्क्रिप्शन प्रकार:

Required

द्वारा बनाया गया:

SCHERING PLOUGH SANTE ANIMALE

चिकित्सीय संकेत:

Treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, paasteurella multocida and haemophilus somnus.Treatment of ovine respiratory tract infections due to Mannheimia haemolytica and Pasteurella multocida susceptible to florfenicol.

प्राधिकरण की तारीख:

2017-02-28

सूचना पत्रक

CONSUMER PACKAGE INSERT FOR A VETERINARY PRODUCT
This medicine is only dispensed with a veterinarian's prescription
For veterinary use only
1. NAME OF THE VETERINARY MEDICINAL PRODUCT, ITS FORM AND STRENGTH
NUFLOR VETERINARY
A solution for injection for cattle and sheep
2. ACTIVE INGREDIENT(S)
Each 1 ml contains the active ingredient: Florfenicol - 300 mg
A list of excipients is detailed in section 13 – “Further
information”.
3. WHAT IS THE MEDICINE INTENDED FOR
Cattle: For treatment of respiratory diseases (BRD) caused by
_Mannheimia haemolytica, _
_Pasteurella multocida_ and_ Haemophilus somnus_.
Sheep: For treatment of respiratory tract infections caused by
_Mannheimia haemolytica _
and_ Pasteurella multocida _susceptible to florfenicol.
THERAPEUTIC GROUP:
Florfenicol is a broad spectrum antibiotic
4. CONTRAINDICATIONS:
Do not use in adult bulls and rams intended for breeding purposes.
Do not use in the case of known hypersensitivity to the active
ingredient or to any of the
excipients.
5. ADVERSE REACTIONS

Cattle: A decrease in food consumption and transient softening of the
feces may occur
during the treatment period. The treated animals recover quickly and
completely upon
termination of treatment. Administration by intramuscular injection
may cause
inflammatory lesions at the injection site
which may persist for 14 days. In very rare
cases, anaphylactic shocks have been reported in cattle.

Sheep: A decrease in food consumption may occur during the treatment
period. The
treated animals recover quickly and completely upon termination of
treatment.
Administration by intramuscular injection may cause inflammatory
lesions at the
injection site
which may persist up to
28 days. Typically, these lesions are mild and
transient.
If you notice any serious effects or other effects not mentioned in
this leaflet, please
inform your veterinary surgeon.
Side effects can be reported to the Ministry of Health by clicking on
the link “Report Side
Effects of Drug Treatment” found on the Ministry of Health hom

उत्पाद विशेषताएं

Page 1 of 5
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
NUFLOR VETERINARY
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains:
ACTIVE SUBSTANCE:
Florfenicol
300 mg
EXCIPIENTS:
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection.
Clear, light yellow to straw-coloured, somewhat viscous solution.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cattle and sheep.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Treatment of bovine respiratory disease (BRD) associated with
_Mannheimia _
_haemolytica_, _Pasteurella multocida_ and _Haemophilus somnus_.
Treatment of ovine respiratory tract infections due to _Mannheimia
haemolytica_ and
_Pasteurella multocida_ susceptible to florfenicol.
4.3
CONTRAINDICATIONS
Do not use in adult bulls and rams intended for breeding purposes.
Do not use in the case of known hypersensitivity to the active
substance or to any of
the excipients listed in section 6.1.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5
SPECIAL PRECAUTIONS FOR USE
Page 2 of 5
Special precautions for use in animals
The product should be used in conjunction with susceptibility testing
and take into
account official and local antimicrobial policies.
The safety of the product has not been established in sheep younger
than 7 weeks of
age.
Special precautions to be taken by the person administering the
veterinary medicinal
product to animals
People with known hypersensitivity to propylene glycol and
polyethylene glycols
should avoid contact with the veterinary medicinal product. In case of
accidental
contact with skin or eyes, rinse immediately with plenty of water.
In case of accidental self-injection, seek medical advice immediately
and show the
package leaflet or the label to the physician.
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
Cattle:
A decrease in food consumption and transient softening of the faeces
may occur
during the treatment period. The treated animals recover quickly and
completely
upon termination of t