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Merck Animal Health

Vista 5 VL5 SQ CFP

Vista 5 VL5 SQ CFP

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Modified-live virus and bacterin combination for the vaccination of healthy cows and heifers, 6 months of age or older, prior to breeding, as an aid in the control of abortions caused by IBR; an aid in the prevention of persistently infected calves caused by BVD 1 and 2; an aid in the control of respiratory disease caused by IBR, BVD 1 and 2, PI3 and BRSV; an aid in reducing infertility caused by Campylobacter fetus (Vibrio); an aid in preventing the 5 most common strains of Lepto, including L. borgpetersenii serovar hardjo-bovis, L. icterohaemorrhagiae and L. Pomona; and an aid in prevention of urinary shedding of L. hardjo organisms. Duration of immunity has been demonstrated to be at least 182 days for IBR and at least 200 days for BVD 1 & 2.

Dosage: 2 ml subcut 14-60 days prior to breeding. Revaccinate annually. Safe for use in pregnant heifers and cows or calves nursing pregnant cows provided the cows and heifers in the herd are vaccinated prior to breeding, within the previous 12 months, with any of the modified live IBR and BVD containing vaccines in this product line. 21 day slaughter withdrawal.

Anaphylactoid reactions may occur. Antidote: Epinephrine.

Manufacturer and/or Label Information

MERCK ANIMAL HEALTH
Intervet Inc.
2 GIRALDA FARMS, MADISON, NJ, 07940
Customer Service: 800-521-5767
Order Desk: 800-648-2118
Technical Service (Companion Animal): 800-224-5318
Technical Service (Livestock): 800-211-3573
Fax: 973-937-5557
Website: www.merck-animal-health-usa.com
THIS SERVICE AND DATA ARE PROVIDED "AS IS". DVMetrics assumes no liability, and each user assumes full risk, responsibility, and liability, related to its use of the DVMetrics service and data. See the Terms of Use for further details.
BOVILIS® Vista® 5 VL5 SQ CFP

Intervet/Merck Animal Health

Bovine Rhinotracheitis-Virus Diarrhea-Parainfluenza 3-Respiratory Syncytial Virus Vaccine, Modified Live Virus, Campylobacter Fetus-Leptospira Canicola-Grippotyphosa-Hardjo-Icterohaemorrhagiae-Pomona Bacterin

Cattle Vaccine

This product has been shown effective for the vaccination of healthy cattle 6 months of age or older against respiratory disease and abortion due to infectious bovine rhinotracheitis (IBR), respiratory disease and fetal infection, including persistently infected calves due to bovine virus diarrhea virus (BVD) Types 1 & 2, bovine respiratory syncytial virus (BRSV) and parainfluenza3 virus (PI3), reproductive disease caused by Campylobacter fetus and leptospirosis (caused by Leptospira canicola, L. grippotyphosa, L. hardjo - including the L. borgpetersenii serovar hardjo bovis, L. icterohaemorrhagiae, and L. pomona). Reproductive Duration of immunity has been shown to be at least 217 days for IBR and at least 206 days for BVD (Types 1 & 2). Respiratory Duration of immunity has been demonstrated to be at least 182 days for IBR, and at least 206 days for BVD Type 1 and at least 200 days for BVD Type 2. Duration of immunity for BRSV, PI3, C. fetus and Leptospira spp. has not been established. For more information regarding efficacy and safety data, go to productdata.aphis.usda.gov.

Respiratory and reproductive efficacy and duration of immunity has been demonstrated against disease caused by the BVD Type 1b strain.

This product has been shown to be effective against urinary shedding of L.hardjo organisms.

SAFETY: Safe for use in pregnant heifers and cows or calves nursing pregnant cows provided the cows and heifers in the herd are vaccinated prior to breeding, within the previous 12 months, with any of the modified live IBR and BVD containing vaccine(s) in this product line.

MIXING DIRECTIONS: Rehydrate freeze dried vial of Vista® 5 SQ with accompanying vial of VL5 SQ. Mix reconstituted vial well.

DIRECTIONS: Shake well and administer a single 2.0 mL dose aseptically by the subcutaneous route 14-60 days prior to breeding. Historically, annual revaccination with this product has been recommended. The need for this booster has not been established. For more information on revaccination frequency, consult your veterinarian.

Mixing Instructions


CAUTION: THE TRANSFER NEEDLE, INCLUDED IN THE CARTON PACKAGING, IS SHARP AND MAY CAUSE INJURY TO SELF OR ANIMALS IF NOT HANDLED OR DISPOSED OF PROPERLY.

1. Insert the transfer needle fully into the small vial of dehydrated vaccine to release the vacuum.

2. Insert the other end of the transfer needle fully into the large vial of sterile diluent.

3. Squeeze enough diluent from the large bottle into the smaller vial to rehydrate the vaccine.

4. With the two bottles still attached, swirl the small vial gently until the vaccine is mixed.

5. With the small vial upside down, squeeze the large bottle several times to draw the mixed vaccine into the large bottle.

6. Separate the bottles and remove the vaccine label from the small vial and apply it to the large bottle for proper identification.

CAUTIONS: Store at 2 to 8°C (35 to 46°F). Fetal health risks associated with the vaccination of pregnant animals with this vaccine cannot be unequivocally determined during clinical trials conducted for licensure. Appropriate strategies to address the risks associated with vaccine use in pregnant animals should be discussed with a veterinarian. Do not freeze. Use entire contents when first opened. Do not use chemical disinfectants to sterilize syringes or needles. Do not mix with other products, except as specified on the label. Inactivate unused contents before disposal. Do not vaccinate within 21 days of slaughter. If allergic reaction occurs, treat with epinephrine. Contains penicillin, streptomycin, and thimerosal as preservatives. In case of human exposure, contact a physician.

FOR ANIMAL USE ONLY

Intervet Inc., d/b/a Merck Animal Health, Omaha, NE 68103 USA

VLN 165A/PCN 44B1.20

1-800-521-5767

For patent information:

http://www.merck.com/product/patent/home.html







Code



20 mL

10 Doses

2 mL per dose

006341

159709-08

100 mL

50 Doses

006342

163920-08

CPN: 1047576.0



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