Ország: Ausztrália
Nyelv: angol
Forrás: APVMA (Australian Pesticides and Veterinary Medicines Authority)
PORCINE CIRCOVIRUS TYPE 2 ORF2 SUBUNIT ANTIGEN
INTERVET AUSTRALIA PTY LIMITED
porcine circovirus type 2
MISC. VACCINES OR ANTI SERA
PORCINE CIRCOVIRUS TYPE 2 ORF2 SUBUNIT ANTIGEN VACCINE-VIRAL Active 2.0 mg/2mL
1 x 100 mL (50 doses); 1 x 20 mL (10 doses); 1 x 200 mL (100 doses); 1 x 50 mL (25 doses); 1 x 500 mL (250 doses); 10 x 20 mL (100 doses); 5 x 20 mL (50 doses)
VM - Veterinary Medicine
INTERVET AUSTRALIA
IMMUNOTHERAPY
Poison schedule: 0; Withholding period: Zero (0) days. EXPORT SLAUGHTER INTER VAL (ESI): Zero (0) days. Before using this product, confirm the current ESI f rom Intervet Australia Pty Limited on 18 00 033 461 or the APVMA website (www.apv ma.gov.au/residues).; Host/pest details: PIG: [PREVENTING WEIGHT LOSS, REDUCED MORTALITY, REDUCTION OF LYMPHOID DEPLETION ]; Poison schedule: 0; Withholding period: WHP: Zero (0) days. ESI: ESI not requi red.; Host/pest details: PIG: [PREVENTING WEIGHT LOSS, REDUCED MORTALITY, REDUCTION OF LYMPHOID DEPLETION ]; Poison schedule: 0; Withholding period: ; Host/pest details: PIG: [PREVENTING WEIGHT LOSS, REDUCED MORTALITY, REDUCTION OF LYMPHOID DEPLETION ]; For active immunisation of pigs to reduce the virus load in blood and lymphoid tissues and to reduce mortality and weight loss associated with Porcine circovirus type 2 related infection (PCVD) occurring during the fattening period.
Registered
2023-07-01
PORCILIS PCV VACCINE 64025 / 124319 Product Name: APVMA Approval No: Label Name: PORCILIS PCV VACCINE Signal Headings: FOR ANIMAL TREATMENT ONLY Constituent Statements: Porcine Circovirus Type 2 ORF2 subunit antigen: ≥ 4.5 log2 antibody titre per dose of 2 mL. Also contains: 346 mg light liquid paraffin (adjuvant) 25 mg dl-α-tocopheryl acetate (adjuvant) Claims: For active immunisation of pigs to reduce the virus load in blood and lymphoid tissues and to reduce mortality and weight loss associated with Porcine circovirus type 2 related infection (PCVD) occurring during the fattening period. Onset of immunity: 2 weeks Duration of immunity: 22 weeks A single dose breaks through up to medium levels of maternally derived antibodies in piglets. A double dose breaks through medium to high levels of maternally derived antibodies. Net Contents: 1 x 20 mL (10 doses) 5 x 20 mL (50 doses) 10 x 20 mL (100 doses) 1 x 50 mL (25 doses) 1 x 100 mL (50 doses) 1 x 200 mL (100 doses) 1 x 500 mL (250 doses) Directions for Use: Restraints: DO NOT mix with any other vaccine or immunological product. Contraindications: RLP APPROVED Precautions: Side Effects: In laboratory studies and field trials: A transient rise in body temperature may occur until 2 days after vaccination. Some piglets may be depressed and show a reduced feed intake for up to 5 days. A transient local reaction at the injection site may be observed in the form of a hard and sometimes warm swelling (up to a diameter of 7cm) diminishing over a period of approximately 14-21 days. A hypersensitivity-like reaction may occur; the animals will recover in several minutes without further treatment. In post marketing experience: In very rare cases anaphylactic-type reactions can occur, which may be life-threatening. In the event of such reactions, treatment may be needed. Dosage and Administration: READ THE ENCLOSED LEAFLET BEFORE USING THIS PRODUCT. SHAKE WELL BEFORE USE. USE THE ENTIRE CONTENTS WITHIN 8 HOURS OF OPENING. The vaccine is a liquid and ready-to-use product. Be Olvassa el a teljes dokumentumot