EFICUR ANTIBIOTIC SUSPENSION FOR INJECTION FOR CATTLE

国家: 澳大利亚

语言: 英文

来源: APVMA (Australian Pesticides and Veterinary Medicines Authority)

有效成分:

CEFTIOFUR AS CEFTIOFUR HYDROCHLORIDE

可用日期:

LABORATORIOS HIPRA S.A.

药物剂型:

PARENTERAL LIQUID/SOLUTION/SUSPENSION

组成:

CEFTIOFUR AS CEFTIOFUR HYDROCHLORIDE ANTIBIOTIC Active 50.0 mg/ml

每包单位数:

100ml; 250ml; 50mL

类:

VM - Veterinary Medicine

治疗领域:

ANTIBIOTIC & RELATED

產品總結:

Poison schedule: 4; Withholding period: MEAT: DO NOT USE less than 3 days before slaughter for human consumption. MILK: Zero (0) days. EXPORT SLAUGHTER INTERV AL (ESI): DO NOT USE less than 8 days be fore slaughter for export. Before using this product, confirm the current ESI fr om the distributor on 02 9810 1104 or th e APVMA website (www.apvma.gov.au/residu es).; Host/pest details: CATTLE - BEEF: [HISTOPHILUS SOMNI, MANNHEIMIA HAEMOLYTICA, PASTEURELLA MULTOCIDA]

授权状态:

Registered

授权日期:

2019-07-01

资料单张

EFICUR ANTIBIOTIC SUSPENSION FOR INJECTION FOR CATTLE
85425/113257
Product Name:
APVMA Approval No:
Label Name:
EFICUR ANTIBIOTIC SUSPENSION FOR INJECTION FOR CATTLE
Signal Headings:
PRESCRIPTION ANIMAL REMEDY
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL TREATMENT ONLY
READ SAFETY DIRECTIONS BEFORE OPENING OR USING
Constituent
Statements:
50 mg/mL Ceftiofur (as ceftiofur hydrochloride)
Claims:
For treatment of bacterial respiratory disease in cattle associated
with Mannheimia
haemolytica, Pasteurella multocida and Histophilus somnus.
Net Contents:
50mL, 100mL, 250mL.
Directions for Use:
Restraints:
DO NOT USE for mass medication; for individual animal treatment only.
DO NOT USE by intramammary, topical or oral route in food producing
animals.
DO NOT USE for the treatment of mastitis in dairy cattle.
DO NOT USE in bobby calves.
DO NOT re-treat animals for 4 days after last treatment program.
Contraindications:
Use is contraindicated in cases of known resistance or
hypersensitivity to the
cephalosporins or beta-lactam antibiotics.
Precautions:
Use with caution in pregnant cattle. The safety of EFICUR has not been
established
during pregnancy. Use only according to the benefit/risk assessment by
the prescribing
veterinarian.
Side Effects:
Hypersensitivity reactions unrelated to dose can occur. Allergic
reactions (e.g. skin
reactions, anaphylaxis) may occasionally occur. Treat symptomatically. RLP APPROVED
In cattle, no signs of systemic toxicity have been observed following
substantial parenteral
overdosages of ceftiofur. Mild inflammatory reactions at the injection
site, such as tissue
oedema and discoloration of the subcutaneous tissue and/or fascial
surface of the muscle
may be observed. Clinical resolution is reached in most animals by 10
days after injection
although slight tissue discoloration may persist for 28 days or more.
Dosage and
Administration:
Shake well before use
Use the contents within 28 days of first broaching of the bottle.
Discard the unused portion.
1 mg ceftiofur/kg bw/day (1 mL EFICUR/50kg bw/da