Země: Kanada
Jazyk: francouzština
Zdroj: Health Canada
Ivermectine
BOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.
Sans
10MG
Solution
Ivermectine 10MG
Sous-cutanée
15G/50G
En vente libre
Bétails; Bétails; Bétails; Porcs; Mouton
objet
Numéro de groupe d'ingrédients actifs (GIA) :0124785002
APPROUVÉ
1998-10-02
INDICATIONS For the treatment of infections and infestations due to internal and external parasites in cattle and swine, and parasitic infections due to internal parasites in sheep. See package insert for complete list of parasites. DOSAGE AND ADMINISTRATION Cattle and Sheep: 1 mL of Ivomec® (10 mg of ivermectin) per 50 kg of body weight by subcutaneous injection only (maximum of 10 mL per site). Swine: 1 mL of Ivomec® (10 mg of ivermectin) per 33 kg of body weight by subcutaneous injection in the neck only. See package insert for complete use directions. CAUTION 1. Do not administer intravenously or intramuscularly. 2. A transitory discomfort has been observed in some animals following subcutaneous administration. A low incidence of soft tissue swelling at the injection site has been observed. These reactions have disappeared without treatment. Divide doses greater than 10 mL between injection sites to reduce occasional discomfort or site reaction. Different sites should be used for other parenteral products. 3. Sheep: Following subcutaneous injections activity suggesting pain, sometimes intense but usually transient, has been seen in some sheep. Adequate vaccination against clostridial infections in sheep is recommended. Consult your veterinarian for advice on a vaccination program. 4. Cattle: To prevent potential secondary reactions when treating infections with cattle grubs, consult your veterinarian on the correct timing of treatment. STORAGE Store bottle in carton to protect from light. 1. Les bovins et les moutons traités ne doivent pas être abattus à des fins alimentaires dans un délai d’au moins trente-cinq (35) jours après le dernier traitement avec ce médicament; les porcs traités ne doivent pas être abattus à des fins alimentaires dans un délai d’au moins vingt-huit (28) jours après le dernier traitement avec ce médicament. 2. Les vaches laitières taries ne doivent pas être traitées avec ce médicament durant les deux (2) mois qui précèdent le vêlage. 3. Ne pas administrer aux Přečtěte si celý dokument