Florfenicol Injection 30% for Veterianry Use Only

• Customization: Available
• Varieties: General Disease Prevention Medicine
• Component: Chemical Synthetic Drugs
• Model NO.: 30%
• Pharmacodynamic Influential Factors: Animal Species
• Storage Method: Moisture Proof
• GMP: Yes
• OEM: Yes
• Transport Package: Carton
• Specification: 10ML, 50ML, 100ML, 250ML, 500ML
• Trademark: GETION
• Origin: China
• HS Code: 3004909099
• Production Capacity: 40000/Day

Product Description

• Composition
• Contains per ml:
• Florfenicol
  300 mg.
• Excipients ad
  1 ml.

Description

Florfenicol is a synthetic broad-spectrum antibiotic effective against most Gram-positive and Gram-negative bacteria isolated from domestic animals. Florfenicol acts by inhibiting protein synthesis at the ribosomal level and
is bacteriostatic. Laboratory tests have shown that florfenicol is active against the most commonly isolated bacterial pathogens involved in bovine respiratory disease which include Mannheimia haemolytica, Pasteurella multocida,
Histophilus somni and Arcanobacterium pyogenes, and against the bacterial pathogens most commonly isolated in respiratory diseases in pigs, including Actinobacillus pleuropneumoniae and Pasteurella multocida.

Contra indications

Not for use in cattle producing milk for human consumption.
Not to be used in adult bulls or boars intended for breeding purposes.
Do not administer in cases of previous allergic reactions to florfenicol.

Side effects

In cattle, a decrease in food consumption and transient softening of the faeces may occur during the treatment period. The treated animals recover quickly and completely upon termination of treatment. Administration of the product by the intramuscular and subcutaneous routes may cause inflammatory lesions at injection site which persist for 14 days.

In swine, commonly observed adverse effects are transient diarrhoea and/or peri-anal and rectal erythema/oedema which may affect 50% of the animals. These effects can be observed for one week. Transient swelling lasting up to 5 days may be observed at the site of injection. Inflammatory lesions at the injection site may be seen up to 28 days.

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