Tilimax
Tilimax merges the potency of Tilmicosin, derived from Tylosin, with the anti-inflammatory prowess of Meloxicam. Ideal for infections in cattle such as pneumonia, keratoconjunctivitis, and foot rot, Tilmicosin targets pathogens like Pasteurella and Mycoplasma. Meloxicam complements the treatment by reducing inflammation and alleviating pain, ensuring comprehensive relief for your animals.
Tilimax stands as a precise solution for a spectrum of infections in livestock. Tilmicosin's enhanced antibacterial activity covers various germs including Pasteurella and Actinobacillus spp, while Meloxicam provides quick relief from inflammation and pain. Choose Tilimax for rapid and effective intervention, promoting your cattle's well-being.
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Description
Description
Each 1 ml contains :
Tilmicosin (as phosphate) 300 mg
Meloxicam 20 mg
- Infections caused by agents sensitive to Tilmicosin specifically Pneumonia , Keratoconjuntivitis and Foot Rot in Cattle.
- Among other germs sensitive to Tilmicosin, we can mention the following ones as important for veterinary medicine : Actinobacillus spp, Pasteurella spp, Bacteroides nodosus , Bacteroides melaninogenicus , Haemophilus spp , Moraxella bovis , Fusobacterium necrophorum , Mycoplasma.
- Meloxicam reduces inflammation symptoms and relieves pain .
Cattle.
Administered by subcutaneous injection only.
Pneumonia : 1 ml Tilimax / 30 kg bodyweight.
Keratoconjuntivitis and Foot Rot : 1 ml Tilimax / 30-60 kg bodyweight.
Administer one dose by subcutaneous .
- Do not administer by intravenous route since it may be fatal in Cattle .
- Do not administer to other animal species. Only administer to Cattle .
- Tilmicosin has been shown to be fatal in Swine , Non-human Primates and potentially fatal in Horses .Do not administer to Swine , Horses , Dairy Cattle in milk or pregnant cows.
- Do not administer simultaneously with other Steroid/Anti-inflammatories or Anti-coagulants .
- Do not administer to animals with alteration of Hepatic ,Cardiac or Renal function .
- Do not administer to animals with haemorrhagic disorder or if there is evidence of gastrointestinal ulcerogenic injuries or individual hypersensitivity to the product .
- Avoid the use in animals with sign of severe dehydration , hypovolaemia , hypotention , since a potential risk of an increase in renal toxicity may be produced .
- In case of secondary effects interrupt treatment .
- Do not slaughter treated animals for human consumption within 28 days from last treatment.
- Do not administer to Female Dairy Cattle 20 months of age or older .
- Do not administer to Calves younger than 1 month of age or fed only with milk
Store at a temperature below 30°C
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