Once PMH SQ

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.
Deactivated - Content may be out of date
This product has been replaced with Bovilis® Once PMH® SQ (Intervet/Merck Animal Health)
Once PMH® SQ

Intervet/Merck Animal Health

MANNHEIMIA HAEMOLYTICA - PASTEURELLA MULTOCIDA VACCINE

Avirulent Live Culture

Cattle Vaccine

Product Description: The reconstituted vaccine product contains avirulent live cultures of Mannheimia haemolytica and Pasteurella multocida.

Indications: For the vaccination of healthy cattle, 3 months of age or older, as an aid in the control of respiratory disease caused by Mannheimia haemolytica and Pasteurella multocida. Duration of Immunity (DOI) has been demonstrated to be at least 16 weeks for Mannheimia haemolytica and Pasteurella multocida. Calves nursing immune-dams should be vaccinated when maternal antibody levels will allow active immunization.

Mixing Directions: 10 Doses - Rehydrate freeze dried vial of Once PMH® SQ with accompanying vial of diluent. Mix reconstituted vial well.

50 Doses - Rehydrate freeze dried vial of Once PMH® SQ with part of the accompanying vial of diluent using the transfer needle provided (see pictorial directions). Mix reconstituted vial well and transfer rehydrated vaccine into diluent vial using transfer needle. Remove transfer needle from former diluent vial and mix reconstituted vial well. Peel label from bottle of Once PMH® SQ and place on diluent vial containing all vaccine.

Use Directions: Inject 2.0 mL subcutaneously to healthy cattle 3 months of age or older. Annual revaccination is recommended. A revaccination dose can be administered at more frequent intervals based upon individual farm disease risk assessment or any time epidemic conditions exist or are reported. 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 needle beyond breather valve into the vial of lyophilized vaccine to remove vacuum.

2. Turn the vial of lyophilized vaccine upside down and fully insert needle into the sterile diluent bottle. Be sure to clear cap with breather valve.

3. Turn attached vial and bottle so the vial of lyophilized vaccine is underneath the sterile diluent bottle and squeeze enough sterile diluent into the vial of lyophilized vaccine to rehydrate the vaccine. Mix well.

4. Turn attached bottles so rehydrated vaccine is above the sterile diluent bottle. Squeeze air into rehydrated vaccine vial.

5. Squeeze and release the sterile diluent bottle until all the solution in the rehydrated vaccine vial drains into the sterile diluent bottle.

6. Separate the vial of lyophilized vaccine and needle from the sterile diluent bottle. Using the tab, remove the back of the vaccine vial label. Place the separated label over the sterile diluent bottle label to accurately identify the newly created solution.

Cautions: Store at 2°-7°C (35°-45°F). Do not freeze. Use immediately after reconstitution; do not save partial contents. Burn the containers and all unused product. Use only in healthy cattle. Do not vaccinate within 21 days before slaughter. If allergic reaction occurs, treat with epinephrine. Contains streptomycin as a preservative.

FOR ANIMAL USE ONLY

Intervet Inc., Merck Animal Health, division of Intervet Inc., Omaha, NE 68103 USA

U.S. Vet Lic. No. 165A

1 800 521-5767

For patent information:

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





Code



10 Doses

20 mL

006337

137239-06

50 Doses

100 mL

006338

135075-05

CPN: 1047445.4



COLORADO SERUM COMPANY4950 YORK STREET, P.O. BOX 16428, DENVER, CO, 80216-0428Telephone: 303-295-7527Order Desk: 800-525-2065Fax: 303-295-1923Website: www.colorado-serum.comEmail: colorado-serum@colorado-serum.comTHIS 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.

TETANUS TOXOID-CONCENTRATED

Colorado Serum

Adjuvanted

GENERAL INFORMATION: This product has been shown to be effective for the vaccination of healthy horses, cattle, sheep, goats, and swine against tetanus. This product was licensed prior to the requirement to establish a minimum age for use. The duration of immunity is unknown. For more information regarding efficacy and safety data, see productdata.aphis.usda.gov.

Safety in pregnant animals is unknown.

Tetanus Toxoid is prepared by detoxifying tetanus toxin in such a manner as to allow the antigenic properties to remain intact. Product is purified, concentrated and adjuvanted to provide a low dose effective immunizing agent.

Each serial is tested for purity, safety, and potency in accordance with USDA requirements.

Tetanus is caused by a neurotoxin produced by growth of Clostridium tetani, an anaerobic (lives without air) micro-organism, in necrotic tissue. Affected animals become stiff, have difficulty swallowing, and have an increased pulse rate. Breathing is labored. Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw.

Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw. Thus, the term “lockjaw” is often used. Legs and tail are often stiff with abdominal muscles contracted. Tetanus stricken animals may be unusually sensitive to light and heat. Temperature of the animal generally remains normal, elevating only shortly before death.

Protective antibody levels usually occur about two weeks after the second injection of the primary immunization series. In contrast, administration of Tetanus Antitoxin is recommended for immediate, emergency, passive treatment of exposed animals with unknown vaccination history or with signs of tetanus infection.

DIRECTIONS: Do not vaccinate within 21 days before slaughter. Store at 2-8° C. Do not freeze. Do not mix with other products. Shake well before use. Use entire contents when first opened.

PRECAUTIONS: A transitory local reaction may occur at injection site. Anaphylactoid reaction may occur following administration of products of this nature. If noted, administer adrenalin or equivalent. In case of human exposure, consult a physician.

DOSAGE & ADMINISTRATION: For primary immunization, two doses should be administered subcutaneously or intramuscularly approximately 30 days apart. Use intramuscularly for horses as local reactions are more likely to occur if injected subcutaneously.

Horses: 1 ml IM

Cattle: 1 ml SC or IM

Sheep, Goats, Swine: 0.5 ml SC or IM

Historically, annual single dose revaccination has been recommended. Contact veterinarian for advice.

OTHER INFORMATION: Contains thimerosal and formalin as preservatives. Tetanus Toxoid Concentrate is available in single dose size packaged 10 vials to the carton, and in 10 dose vials.

THE PEAK OF QUALITY SINCE 1923

VLN: 188 / PCN: 8601.00

COLORADO SERUM COMPANY, 4950 York Street, Denver, Colorado 80216

303-295-752

www.colorado-serum.com

Contact us for information on other Colorado Serum Company products. Fine Veterinary Products since 1923.

FOR VETERINARY USE ONLY

Order #

10 - 1 ml vials

10 - 1 dose vials

11411

10 ml

10 doses

11415

CPN: 1101033.3