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Trimidox (Canada)

This page contains information on Trimidox for veterinary use.
The information provided typically includes the following:
  • Trimidox Indications
  • Warnings and cautions for Trimidox
  • Direction and dosage information for Trimidox

Trimidox

This treatment applies to the following species:
Company: Vetoquinol

(Trimethoprim-Sulfadoxine)

Sterile Injectable Solution

DIN 02184559

Veterinary Use Only

Description

A clear, yellow aqueous solution for parenteral administration.

The active ingredients of TRIMIDOX are a combination of trimethoprim and sulfadoxine which has been established in a ratio of 1:5.

(Dosage Form): TRIMIDOX is a solution containing 4% W/V trimethoprim and 20% W/V sulfadoxine in an organic solvent.

Each mL contains 40 mg of trimethoprim and 200 mg of sulfadoxine.

Chlorocresol is used as a preservative at a concentration of 1mg/mL (0.1% W/V).

Pharmacology

(Action) TRIMIDOX contains trimethoprim, a synthetic antibacterial and sulfadoxine, a sulphonamide. The two components of TRIMIDOX produce a sequential double blockade of bacterial metabolism, giving a level of activity many times greater than that obtained by either drug alone.

TRIMIDOX provides effective antibacterial activity against a wide range of infections caused by Gram-positive and Gram-negative bacteria.

TRIMIDOX has shown activity in vitro against the following organisms.

VERY SENSITIVE ORGANISMS:

Escherichia coli, Bacillus anthracis, Clostridium spp., Pasteurella spp., Shigella spp., Haemophilus influenzae, Salmonella spp., Streptococcus zooepidemicus, Proteus mirabilis, Vibrio spp.

SENSITIVE ORGANISMS:

Streptococcus viridans, Klebsiella spp., Brucella spp., Proteus spp., Enterocci spp., Actinomyces, Staphylococcus aureus (including penicillinase-producing organisms), Corynebacterium spp., Bordetella spp., Neisseria spp.

MODERATELY SENSITIVE ORGANISMS:

Enterobacter aereogenes, Nocardia spp.

NON-SENSITIVE ORGANISMS:

Pseudomonas aeruginosa*, Leptospira spp., Mycobacterium tuberculosis, Erysipelothrix rhusiopathiae.

*usually non-sensitive.

Trimidox Indications

TRIMIDOX may be used in cattle and swine where potent systemic antibacterial action against a wide range of sensitive organisms is required.

TRIMIDOX is indicated in CATTLE for the treatment of:

RESPIRATORY TRACT INFECTIONS: Bacterial pneumonias including bovine pneumonia pasteurellosis (shipping fever).

ALIMENTARY TRACT INFECTIONS: Primarily enteric and septicaemic colibacillosis and salmonellosis.

OTHER INFECTIONS: Infectious pododermatitis (foot rot, foul in the foot) and septicaemias.

TRIMIDOX is indicated in SWINE for the treatment of:

RESPIRATORY TRACT INFECTIONS: Bacterial pneumonias.

ALIMENTARY TRACT INFECTIONS: Colibacillosis and post-weaning scours.

OTHER INFECTIONS: Mastitis-metritis-agalactia syndrome of sows (MMA) and bacterial arthritis.

Dosage and Administration

TRIMIDOX should be administered at a dose rate of 1 mL per 15 kg body weight daily. In piglets weighing less than 4.5 kg do not exceed a dose of 0.5 mL.

Intramuscular injection is recommended for cattle and swine, but if a particularly rapid response is required in acute infections TRIMIDOX can be administered by slow intravenous injection.

Treatment should continue for 2 - 3 days after symptoms have subsided. The usual course of treatment is no longer than 5 consecutive days.

Contraindications

TRIMIDOX should not be used in cattle or swine showing marked liver parenchymal damage or blood dyscrasias, nor in those with history of sulphonamide sensitivity.

CAUTIONS:

With intravenous therapy generally, and sulphonamides in particular, hypersensitivity reactions can occur and should be appropriately treated with corticosteroids or epinephrine.

Temporary local irritation and swelling are encountered occasionally after intramuscular injection of TRIMIDOX.

Injections should not be given by routes other than those recommended.

Warnings

Milk taken from treated animals during treatment and within 96 hours after the latest treatment must not be used as food. Treated animals must not be slaughtered for use in food for at least 10 days after the latest treatment with this drug.

Side Effects

(Adverse Reactions): No significant adverse reactions have been reported.

STORAGE CONDITIONS:

Store between 15°C and 25°C. Protect from light.

PRESENTATION:

Available in 100 mL (code 25737), 250 mL (code 25738) and 500 mL (code 25739) vials.

CONTAINS ANTIMICROBIAL

USE RESPONSIBLY

Vetoquinol N.-A. Inc., 2000, ch. Georges, Lavaltrie, QC, Canada J5T 3S5

Net

Code

 

100 mL

25737

216551C05

331491I01

026491L08

250 mL

25738

216552C05

331491I01

027491L08

500 mL

25739

216553C05

029491I11

028491L08

CPN: 1234149.7

VETOQUINOL N.-A. INC.
Commercial Division

2000, CHEMIN GEORGES, LAVALTRIE, QC, J5T 3S5
Telephone:   450-586-2252
Order Desk:   800-363-1700
Fax:   450-586-4649
Website:   www.vetoquinol.ca
Email:   info@vetoquinol.ca
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