TULAJECT SOLUTION

Land: Canada

Sprog: engelsk

Kilde: Health Canada

Aktiv bestanddel:

TULATHROMYCIN

Tilgængelig fra:

ALIVIRA ANIMAL HEALTH LIMITED

Dosering:

100MG

Lægemiddelform:

SOLUTION

Sammensætning:

TULATHROMYCIN 100MG

Indgivelsesvej:

SUBCUTANEOUS

Enheder i pakken:

100

Recept type:

Prescription

Terapeutisk gruppe:

CATTLE; CATTLE; CATTLE; CATTLE; SWINE (PIGS); SHEEP

Produkt oversigt:

Active ingredient group (AIG) number: 0151667001

Autorisation status:

APPROVED

Autorisation dato:

2023-03-16

Indlægsseddel

Dieline box Tulaject 250 ml
67 x 147 x 67 mm
Dieline
Varnish-free
147 mm
67 mm
67 mm
TULAJECT
Veterinary Use Only
Antibiotic for cattle, swine
and sheep
PR
TM
DIN XXXXXXXX
Sterile
100 mg of tulathromycin/mL
Keep out of reach of children.
NET: 250 ML
WARNINGS: Treated animals must not be slaughtered for use
in food for at least 44 days in cattle, 8 days in swine and 16
days in sheep, after the latest treatment with this drug. Do not
use in dairy cows 20 months of age and older. To limit the
development of antimicrobial resistance, Tulaject should only
be used (1) as an arrival treatment in feedlot calves when BRD
has been diagnosed and calves are at high risk of developing
BRD, and (2) for control of SRD outbreak when groups of pigs
are at high risk of developing SRD.
Indications: _Beef and Non-lactating Dairy Cattle:_ For the
treatment of bovine respiratory disease (BRD) and for the
reduction of morbidity associated with BRD in feedlot calves
during the first 14 days in the feedlot when administered at the
time of arrival. For the treatment of infectious bovine keratocon-
junctivitis (IBK). For the treatment of bovine foot rot (interdigital
necrobacillosis).
NOTE: To reduce the possibility of excess trim at the injection
site it is recommended that swine not be slaughtered for up to
35 days after the latest treatment with this drug.
Active Ingredient: Tulathromycin, 100 mg/mL
Preservative: Monothioglycerol 5 mg/mL
_Suckling Calves, Dairy Calves, and Veal _
_Calves:_ For the treatment of BRD.
_Swine:_ For the treatment of swine respiratory disease (SRD)
and for the control of SRD ingroups of pigs where SRD has
been diagnosed.
_Sheep:_ For the treatment of foot rot.
See package insert for the complete list of bacteria susceptible
to tulathromycin in cattle, swine and sheep.
Dosage and Administration: Administer in the neck by
subcutaneous injection in cattle and intramuscular injection in
swine and sheep, a single dose of 2.5 mg/kg body weight. Do
not inject more than 10 mL for cattle and 2.5 mL for swine and
sheep