Pneumomune-Re (Rhodococcus Equi Antibody)This page contains information on Pneumomune-Re (Rhodococcus Equi Antibody) for veterinary use.
The information provided typically includes the following:
- Pneumomune-Re (Rhodococcus Equi Antibody) Indications
- Warnings and cautions for Pneumomune-Re (Rhodococcus Equi Antibody)
- Direction and dosage information for Pneumomune-Re (Rhodococcus Equi Antibody)
Pneumomune-Re (Rhodococcus Equi Antibody)This treatment applies to the following species:
Rhodococcus Equi Antibody
For Veterinary Use, Not Intended for Humans
300 ml, 500 ml, 1000 ml
For intravenous use in the prevention or reduction in severity of Rhodococcus equi pneumonia in the equine neonate in the equine neonate by prophylactic treatment. The average 100lb. foal should receive 1 liter within the first 24 hours of life. A second 1 liter dose should be administered approximately three weeks later. In endemic areas an additional dose may be necessary for foals up to 16 weeks of age.
KEEP FROZEN AT ≤-15C UNTIL USE. Thaw quickly in warm water not exceeding 110F. DO NOT MICROWAVE. Administer as soon as possible after thawing to body temperature by filtered intravenous infusion at a maximum rate of 20ml/kg (shock bolus) over a period of 15-20 minutes. Do not mix with other products, except as specified on the label.
In case of a reaction, marked most often by tenesmus and hyperventilation, slow the speed of administration. If this does not abate the signs, stop administration until signs abate and continue at a slower rate. If signs persist, suspend administration and treat with histamine blockers and anti-inflammatory agents. Discard any unused portion.
Each single dose bag contains plasma as a source of Rhodococcus equi antibodies with sodium citrate as an anticoagulant derived from healthy horses with Aa and Ca r.b.c. antigens and no r.b.c antibodies. All donor horses are negative for EIA, EVA, Dourine, Brucellosis, Piroplasmosis and Glanders. There is no preservative added.
CAUTION: Anaphylaxis may occur. This product has not been processed by heating or treating with ionizing radiation and may be capable of spreading disease. The use of equine serum and plasma products has been associated with hepatitis (Theiler’s Disease). This product has not been tested in pregnant animals. In case of human exposure contact a physician.
US Vet. Lic. No. 318, Product Code 3750.00
LAKE IMMUNOGENICS, INC. ONTARIO, NY 14519
348 BERG ROAD, ONTARIO, NY, 14519
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