John Martin Argentina

Meloxivet Inyectable

Non-steroidal anti-inflammatory drug

Meloxicam exerts potent, selective inhibitory activity on Cyclooxygenase-2 (COX-2), both in vivo and in vitro, within the prostaglandin biosynthetic cascade. This selective and specific COX-2 blockade has demonstrated anti-inflammatory, analgesic, anti-exudative, and antipyretic properties, with minimal gastrolesive or ulcerogenic effects.

Meloxivet inyectable
TARGET SPECIES
Dogs and cats.
DOSAGE FORM
Injectable solution.
HOW SUPPLIED
10 mL vial.
DIFFERENTIATORS

BENEFITS AND COMPETITIVE ADVANTAGES

Useful when oral administration is not possible.
Rapid onset of action

Rapid onset of action

Useful when oral administration is not possible.

Rapid onset of action

TECHNICAL DETAILS

Information

– Meloxicam 5 mg.
– Excipients q.s. to 1 ml.
Administrar por vía SC.
Dogs: 0.2 mg/kg on the first day, then 0.1 mg/kg on subsequent days.
Cats: to prevent postsurgical pain and inflammation, an initial premedication dose of 0.3 mg/kg may be given, followed 24 hours later by 0.1 mg total. Dosage and treatment duration may be adjusted based on the clinical picture, at the discretion of the attending veterinary professional.

Meloxivet Inyectable

TARGET SPECIES
Dogs and cats.
DOSAGE FORM
Injectable solution.
HOW SUPPLIED
10 mL vial.
Non-steroidal anti-inflammatory drug

Meloxicam exerts potent, selective inhibitory activity on Cyclooxygenase-2 (COX-2), both in vivo and in vitro, within the prostaglandin biosynthetic cascade. This selective and specific COX-2 blockade has demonstrated anti-inflammatory, analgesic, anti-exudative, and antipyretic properties, with minimal gastrolesive or ulcerogenic effects.

Useful when oral administration is not possible.
Rapid onset of action

Rapid onset of action

Useful when oral administration is not possible.

Rapid onset of action

TECHNICAL DETAILS

Information

– Meloxicam 5 mg.
– Excipients q.s. to 1 ml.
Administrar por vía SC.
Dogs: 0.2 mg/kg on the first day, then 0.1 mg/kg on subsequent days.
Cats: to prevent postsurgical pain and inflammation, an initial premedication dose of 0.3 mg/kg may be given, followed 24 hours later by 0.1 mg total. Dosage and treatment duration may be adjusted based on the clinical picture, at the discretion of the attending veterinary professional.
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