LANFLOX 100 MGML VETERINARY

Land: Israel

Språk: engelsk

Kilde: Ministry of Health

Aktiv ingrediens:

ENROFLOXACIN

Tilgjengelig fra:

ROMAT LTD

Legemiddelform:

SOLUTION (ORAL)

Sammensetning:

ENROFLOXACIN 100 MG / 1 ML

Administreringsrute:

PER OS IN DRINKING WATER

Resept typen:

Required

Produsert av:

LABORATORIOS KARIZOO S.A., SPAIN

Indikasjoner:

Treatment of infections caused by the following bacteria susceptible to enrofloxacin:ChickensMycoplasma gallisepticum, Mycoplasma synoviae,Avibacterium paragallinarum, Pasteurella multocida.TurkeyMycoplasma gallisepticum, Mycoplasma synoviae, Pasteurella multocida.Enrofloxacin should be used only after sensitivity of the bacteria has been confirmed and there is no alternative therapy (due to resistance to other antibiotics).

Autorisasjon dato:

2022-12-31

Informasjon til brukeren

PACKAGE LEAFLET FOR A VETERINARY PRODUCT
This medicine is marketed according to a veterinarian’s prescription
only
For animal use only
1.
NAME OF VETERINARY MEDICINE, FORM AND STRENGTH:
Lanflox 100 mg/mL veterinary, solution for administration in drinking
water
2.
ACTIVE INGREDIENTS and their concentration in a dose unit: each mL
contains: Enrofloxacin 100 mg
For the list of excipients, please see section 13.
3.
WHAT IS THE MEDICINE INTENDED FOR: Treatment of infections caused by
the following bacteria susceptible to enrofloxacin:
Broilers: Mycoplasma gallisepticum, Mycoplasma synoviae,Avibacterium
paragallinarum, Pasteurella multocida.
Turkey: Mycoplasma gallisepticum, Mycoplasma synoviae, Pasteurella
multocida.
Enrofloxacin should be used only after sensitivity of the bacteria has
been
confirmed and there is no alternative therapy (due to resistance to
other
antibiotics).
Therapeutic group: fluoroquinolones.
4.
CONTRAINDICATIONS: Not to be used for prevention. Do not use in the
event of known resistance or cross-resistance to quinolones in animals
that are candidates for treatment. If there is known hypersensitivity
to the
active substance, to other quinolones or to any of the excipients,
avoid
treatment with this product.
5.
SIDE EFFECTS can be reported to the Ministry of Health by clicking on
the
link "Adverse Drug Reactions Repot" that appears on the home page of
the Ministry of Health web site (www.health.gov.il), which leads to an
online form for reporting side effects. Alternatively you can use the
following link: https://sideeffects.health.gov.il/_ _
6.
TARGET SPECIES: Broilers and turkeys.
7.
DOSAGE AND ADMINISTRATION FOR EACH TARGET SPECIES: In drinking water:
10 mg/kg per day in drinking water for 3 - 5 consecutive days,
equivalent
to 0.1 ml of the product per 1 kg body weight per day. Administer for
5
consecutive days in the event of mixed, progressive and chronic
infections. If no improvement is achieved after 2 - 3 days, an
alternative
antibiotic treatment should be considered based on a sensitiv