EXCEDE STERILE SUSPENSION

Country: অস্ট্রেলিয়া

ভাষা: ইংরেজি

সূত্র: APVMA (Australian Pesticides and Veterinary Medicines Authority)

এখন এটা কিনুন

সক্রিয় উপাদান:

CEFTIOFUR AS CEFTIOFUR CRYSTALLINE FREE ACID

থেকে পাওয়া:

ZOETIS AUSTRALIA PTY LTD

INN (International Name):

ceftiofur (acid)(200mg/mL)

ফার্মাসিউটিকাল ফর্ম:

PARENTERAL LIQUID/SOLUTION/SUSPENSION

রচনা:

CEFTIOFUR AS CEFTIOFUR CRYSTALLINE FREE ACID ANTIBIOTIC Active 200.0 mg/ml

প্যাকেজ ইউনিট:

100 mL; 250 mL

শ্রেণী:

VM - Veterinary Medicine

Manufactured by:

ZOETIS AUSTRALIA

Therapeutic group:

CATTLE | BEEF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | COW | DAIRY COW | HEIFER | STEER

Therapeutic area:

ANTIBIOTIC & RELATED

থেরাপিউটিক ইঙ্গিত:

BOVINE RESPIRATORY DISEASE | SHIPPING FEVER

পণ্য সারাংশ:

Poison schedule: 4; Withholding period: WITHHOLDING PERIODS MEAT: DO NOT USE l ess than 14 days before slaughter for human consumption. Calves born to cows that were treated during pregnancy mu st not be slaughtered for human consump tion for 14 days after treatment of the dam. MILK: Milk may be collected and processed for human consumption at any time after treatment. DO NOT SLAUGHTE R for export less than 14 days after tr eatment. Calves born to cows that were treated during pregnancy must not be s laughtered for export for 14 days afte r treatment of the dam.; Host/pest details: CATTLE: [BOVINE RESPIRATORY DISEASE]; Poison schedule: 4; Withholding period: ; Host/pest details: CATTLE: [BOVINE RESPIRATORY DISEASE]; For the treatment of bovine bacterial diseases caused by Mannheimia haemolytica, Pasteurella multocida & Histophilus somni.See Restraints & WITHHOLDING PERIODS on leaflet.

অনুমোদন অবস্থা:

Registered

অনুমোদন তারিখ:

2023-07-01

তথ্য লিফলেট

                                Product Name:
APVMA Approval No:
EXCEDE STERILE SUSPENSION
65092/126405
Label Name:
EXCEDE STERILE SUSPENSION
Signal Headings:
PRESCRIPTION ANIMAL REMEDY
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL TREATMENT ONLY
READ SAFETY DIRECTIONS
Constituent
Statements:
200 mg/mL CEFTIOFUR as Ceftiofur Crystalline Free Acid
Claims:
For the treatment of bovine bacterial respiratory diseases caused by
_Mannheimia _
_haemolytica, Pasteurella multocida_ and_ Histophilus somni. _
Resistance may develop to any antibiotic.
Net Contents:
100 mL, 250 mL
Directions for Use:
Restraints:
ADMINISTER ONLY by injection in base of ear.
DO NOT re-treat animals less than 28 days after the last injection.
DO NOT USE for mass medication: for individual animal treatment only.
DO NOT USE for the treatment of mastitis in dairy cattle.
Contraindications:
As with all drugs, the use of EXCEDE Sterile Suspension is
contra-indicated in animals
previously found to be hypersensitive to the drug.
Precautions:
Side Effects:
Dosage and
Administration:
SHAKE WELL BEFORE USING
Discard unused contents within 28 days of initial vial broaching.
Administer one dose as a single subcutaneous injection in the
posterior aspect of the ear
where it attaches to the head (base of the ear) to cattle at a dosage
of 6.6mg/kg body
weight (3.3mL per 100 kg body weight). RLP APPROVED
Most animals will respond to treatment within three to five days. If
no improvement is
observed, the diagnosis should be re-evaluated.
Administration Technique Base of the Ear
•
Hold the syringe and needle behind the ear so the needle and syringe
point in the
direction of an imaginary line that would pass through the head toward
the
animal’s opposite eye. See Figures 1 and 2.
•
Insert the needle through the loose skin in the posterior aspect of
the ear where it
attaches to the head (base of the ear) while maintaining this angle.
See Figure 1.
•
Deliver the entire contents of the syringe.
FIGURE 1: Subcutaneous administration of EXCEDE Sterile Suspension at
the posterior
aspect of the ear whe
                                
                                সম্পূর্ণ নথি পড়ুন
                                
                            

পণ্য বৈশিষ্ট্য

                                PRODUCT NAME: EXCEDE® STERILE SUSPENSION 
PAGE: 1 OF 5 
THIS REVISION ISSUED: FEBRUARY, 2012 
 
MATERIAL SAFETY DATA SHEET 
Issued by: Pfizer Australia Pty Ltd 
Phone: 1800 814 883
POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800
764 766 IN NEW ZEALAND)
 
SECTION 1 - IDENTIFICATION OF THE MATERIAL AND SUPPLIER 
 
Pfizer Australia Pty Ltd 
 
38-42  Wharf  Road 
 
West Ryde  NSW  2114 
 
Tel:     1800 814 883 
 
Fax:    (02) 9850 3399 
 
____________________________________ 
 
PFIZER AUSTRALIA PTY LTD
 
 
A.B.N. 50 008 422 348 
CHEMICAL NATURE:  
Antibiotic in a suitable vehicle. Injectable.
 
TRADE NAME:  
EXCEDE
®
 STERILE SUSPENSION 
APVMA CODE:  65092 
PRODUCT USE:  
Veterinary product used as an antibiotic. Not for human use.
 
CREATION DATE: 
FEBRUARY, 2012 
THIS VERSION ISSUED: 
FEBRUARY, 2012 and is valid for 5 years from this date. 
SECTION 2 - HAZARDS IDENTIFICATION 
STATEMENT OF HAZARDOUS NATURE  
This product is classified as: Xi, Irritating. Hazardous according
to the criteria of SWA.  
Not a Dangerous Good according to the Australian Dangerous Goods
(ADG) Code.
 
RISK PHRASES: R42/43. May cause sensitisation by inhalation and skin
contact.  
SAFETY PHRASES: S28, S24/25. After contact with skin, wash
immediately with plenty of soap and water. Avoid 
contact with skin and eyes.  
SUSMP CLASSIFICATION: S4 
ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the
ADG Code. 
UN NUMBER: None allocated 
E
E
E
M
M
M
E
E
E
R
R
R
G
G
G
E
E
E
N
N
N
C
C
C
Y
Y
Y
 
 
 
O
O
O
V
V
V
E
E
E
R
R
R
V
V
V
I
I
I
E
E
E
W
W
W
 
 
 
PHYSICAL DESCRIPTION & COLOUR: Suspension. 
ODOUR: Musty odour. 
MAJOR HEALTH HAZARDS: may cause sensitisation by inhalation and
skin contact. This is an antibiotic preparation. 
Any person with a history of allergies to this class of substances
(especially penicillin and cephalosporin) should avoid 
contact with this product as it may cause sensitisation.
                                
                                সম্পূর্ণ নথি পড়ুন
                                
                            

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