Tolfine Injectable Solution 50 Ml

In cattle:
- Reduction of inflammation associated with musculoskeletal and respiratory infections.

CONTRAINDICATIONS

The use of this veterinary medicine is not recommended in the case of heart, liver or kidney failure.
Tolfenamic acid is contraindicated in the case of ulcerations or digestive bleeding.

Do not use in case of hypersensitivity to the active substances or to any of the excipients.

ADVERSE REACTIONS

The frequency of adverse reactions is defined using the following convention: very common (more than 1 in 10 animals treated displaying adverse reaction(s))

-common (more than 1 but less than 10 animals in 100 animals treated)
-uncommon (more than 1 but less than 10 animals in 1,000 animals treated)

- rare (more than 1 but less than 10 animal in 10,000 animals treated)
-very rare (less than 1 animal in 10.000 animals treated, including isolated) reports).

A transient inflammation and tumefaction may appear at the injection site.
If you notice any serious effects or other effects not mentioned in this package leaflet, please inform your veterinary surgeon.

TARGET SPECIES: Cattle.

DOSAGE, ROUTE AND METHOD OF ADMINISTRATION

2 mg per kg bodyweight, i.e. 1 ml per 20 kg bodyweight, by intramuscular injection, to be repeated every 48 hours.

2 mg per kg bodyweight, i.e. 1 ml per 20 kg bodyweight, by intravenous injection, to be repeated every 24 hours, or to be relayed 24 hours later with intramuscular injections.

Do not exceed 5 consecutive injections.

ADVICE ON CORRECT ADMINISTRATION: None known

WITHDRAWAL PERIOD

Intramuscular route:

Meat and offal: 12 days. Milk: zero day.


Intravenous route:

Meat and offal: 4 days. Milk: 12 hours .