MU-SE® Label Information

MU-SE® INJECTION

Cattle

Therapeutic Class

Sub-species

MU-SE® Label Information

(SELENIUM, VITAMIN E)

Injection


FOR VETERINARY USE ONLY


CAUTION
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

 

DIRECTIONS
MU-SE (selenium, vitamin E) is an emulsion of selenium-tocopherol for the prevention and treatment of STD syndrome in weanling calves and breeding beef cattle. Each mL contains: 10.95 mg sodium selenite (equivalent to 5 mg selenium), 50 mg (68 USP units) vitamin E (as d-alpha tocopheryl acetate), 250 mg polysorbate 80, 2% benzyl alcohol (preservative), water for injection q.s. Sodium hydroxide and/or hydrochloric acid may be added to adjust pH.

 

ACTIONS
It has been demonstrated that selenium and tocopherol exert physiological effects and that these effects are intertwined with sulfur metabolism. Additionally, tocopherol appears to have a significant role in the oxidation process, thus suggesting an interrelationship between selenium and tocopherol in overcoming sulfur-induced depletion and restoring normal metabolism. Although oral ingestion of adequate amounts of selenium and tocopherol would seemingly restore normal metabolism, it is apparent that the presence of sulfur and, perhaps other factors interfere during the digestive process with the proper utilization of selenium and tocopherol. When selenium and tocopherol are injected, they bypass the digestive process and exert their full metabolic effects promptly on cell metabolism. Anti-inflammatory action has been demonstrated by selenium-tocopherol in the Selye Pouch Technique and experimentally induced polyarthritis study in rats.


INDICATIONS
MU-SE (selenium, vitamin E) is recommended for the prevention and treatment of STD syndrome in weanling calves and breeding beef cattle. Clinical signs are: Stiffness and lameness; chronic, persistent diarrhea; unthriftiness, abortions and/or weak premature calves.

 

CONTRAINDICATION
Do not use in adult dairy cattle. Premature births and abortions have been reported in dairy cattle injected with this product during the third trimester of pregnancy.


WARNINGS
Anaphylactoid reactions, some of which have been fatal, have been reported in cattle administered the MU-SE product. Signs include excitement, sweating, trembling, ataxia, respiratory distress, and cardiac dysfunction.


Use only as directed in weanling calves and breeding beef cows. Discontinue use 30 days before the treated cattle are slaughtered for human consumption.

 

DOSAGE AND ADMINISTRATION
Inject subcutaneously or intramuscularly. Weanling calves: 1 mL per 200 pounds of body weight. Breeding beef cows: 1 mL per 200 pounds of body weight during the middle third of pregnancy, and 30 days before calving.


CAUTION
Selenium is toxic if administered in excess. A fixed dose schedule is therefore important (read package insert for each selenium-tocopherol product carefully before using).

 

PRECAUTIONS Selenium-Tocopherol Deficiency (STD) syndrome produces a variety and complexity of symptoms often interfering with a proper diagnosis. Even in selenium deficient areas there are other disease conditions which produce similar clinical signs. It is imperative that all these conditions be carefully considered prior to the treatment of STD syndrome. Selenium levels, elevated SGOT, and creatine serum levels may serve as aids in arriving at a diagnosis of STD, when associated with other indices.


Important
Use only the selenium-tocopherol product recommended for each species. Each formulation is designed for the species indicated to produce the maximum efficacy and safety.

 

HOW SUPPLIED 100 mL sterile, multiple dose vial.

 

STORAGE
Store between 2° and 30°C (36° and 86°F).

Protect from freezing.

 

NADA # 30-314, Approved by FDA

 

October 1998

Copyright © 1985, 1996, 1998, Schering-Plough Animal Health Corp., Union, NJ 07083. All rights reserved.

Made in Germany.

Net Contents

NDC

22233203 Rev. 10/98
US 1492 USA006576LA

100 mL

0061-0950-04

 


NAC No.:
10471311