Flunex

Maintains productivity

Flunixin meglumine

A nonsteroidal anti-inflammatory drug, which increases the efficacy of an antibiotic treatment regimen. It makes the recovery period shorter and maintains the productive qualities of cattle and pigs by relieving inflammation and pain.

Powerful analgesic and anti-inflammatory effect

Rapid recovery of productive qualities

Prolonged effect - 24 hours

Anti-inflammatory effect is 16 hours longer as compared to ketoprofen.

Description
A nonsteroidal anti-inflammatory drug, which increases the efficacy of an antibiotic treatment regimen. It makes the recovery period shorter and maintains the productive qualities of cattle and pigs by relieving inflammation and pain.

Flunex is a clear yellow solution.

Packing: 100 mL glass bottles.
Composition
Composition

1 ml
Flunex

50 mg flunixin
Pharmacological properties
Pharmacological properties

Flunixin is a non-selective inhibitor of cyclooxygenase (COX1 and COX2) activity; it also suppresses the synthesis of E2 prostaglandins, that act as inflammatory mediators, thus ensuring its analgesic, anti-inflammatory, antipyretic, and antitoxic activity. After parenteral administration, flunixin is quickly absorbed from the injection site and distributed among the organs and tissues of an animal. Its peak blood concentration is reached in 5 to 45 minutes. The drug accumulates in the focus of inflammation thus prolonging the therapeutic effect for up to 24 hours
Indications
Indications

Flunex is prescribed for horses, cattle and pigs as an anti-inflammatory, analgesic and antipyretic agent within complex therapy of obstetric-gynecologic, gastrointestinal, and respiratory diseases; for pain syndromes, fever, etc. both alone and together with antibacterial agents; to control inflammatory processes secondary to the diseases of the musculoskeletal system; to relieve pain syndrome (of various etiology) in horses, cattle and pigs.

Due to Flunex applied, the recovery period can be reduced by 36 hours, with positive dynamics observed 18 hours earlier compared with a monotherapy.

Due to Flunex applied, the recovery period in the case of suppurative and catarrhal mastitis can be reduced by 12 hours, with positive dynamics observed 9 hours earlier compared with a monotherapy.

Due to Flunex applied, the intensity of symptoms can be reduced in 7 hours, which is 17 hours less than that occurred when a monotherapy is used. Thus, the condition of the animal is quickly improved and the weight gain is stable.

Due to Flunex applied, the recovery period can be reduced by 24 hours compared to a monotherapy, and the temperature is normalized after 30 minutes
Dosage and route of administration

Dosage and route of administration

Animal species	Indications	Route of administration	Dosage	Frequency of administration	Treatment regimen
Cattle	Respiratory disease Acute mastitis Other diseases	Intramuscularly Intravenously	2 mL/45 kg	Once a day	Maximum 5 days
Horses	Musculoskeletal system disorders	Intravenously	1 mL/45 kg	Once a day	Maximum 5 days
	Relief from pain syndrome at colic		1 mL/45 kg	Once	If required, repeat administration at the same dose in 24 hours
	Endotoxemia, septic shock, and other pathologies associated with circulatory disorders in the digestive tract		0,2 mL/ 45 kg	Every 6 to 8 hours	Maximum 5 injections
Pigs	MMA syndrome Respiratory disease	Intramuscularly	2 mL/45 kg	Once

Restrictions
Restrictions

CONTRAINDICATIONS

Hypersensitivity of an animal to the drug components. Avoid using the drug in animals suffering from renal, liver, heart failure, or hypovolemia (except for endotoxemia or septic shock).

Intra-arterial administration of Flunex to animals is prohibited

Due to the increased risk of a painful reaction, avoid administering more than 5 mL of the solution in large animals and 2.5 mLin small animals to a single injection site.

Avoid using the drug in pregnant females, animals younger than 1.5 months, or in pigs with the body weight of less than 6 kg.

Avoid using Flunex concurrently with other anti-inflammatory drugs or nephrotoxic agents.

RESTRICTIONS

After the treatment with Flunex, cattle can be slaughtered for human consumption at least 8 days after the drug was administered intravenously for the last time and 35 days after the drug was administered intramuscularly; horses - at least 8 days; pigs - at least 24 days after the last administration of the drug.

In the case of forced slaughter of animals before the established deadlines, the meat can be used for feeding fur-bearing animals.

The milk, obtained from the treated milked animals, may be used for human consumption no earlier than 60 hours after the last dose of Flunex was administered. Taken before expiration of the restriction period, the milk can be used for animal feeding after boiling.

SHELF LIFE

3 years from the date of manufacture; after first opening - 28 days.

Description
Composition
Pharmacological properties
Indications
Dosage and route of administration
Restrictions

A nonsteroidal anti-inflammatory drug, which increases the efficacy of an antibiotic treatment regimen. It makes the recovery period shorter and maintains the productive qualities of cattle and pigs by relieving inflammation and pain.

Flunex is a clear yellow solution.

Packing: 100 mL glass bottles.

Composition

1 ml

Flunex

50 mg flunixin

Pharmacological properties

Flunixin is a non-selective inhibitor of cyclooxygenase (COX1 and COX2) activity; it also suppresses the synthesis of E2 prostaglandins, that act as inflammatory mediators, thus ensuring its analgesic, anti-inflammatory, antipyretic, and antitoxic activity. After parenteral administration, flunixin is quickly absorbed from the injection site and distributed among the organs and tissues of an animal. Its peak blood concentration is reached in 5 to 45 minutes. The drug accumulates in the focus of inflammation thus prolonging the therapeutic effect for up to 24 hours

Indications

Flunex is prescribed for horses, cattle and pigs as an anti-inflammatory, analgesic and antipyretic agent within complex therapy of obstetric-gynecologic, gastrointestinal, and respiratory diseases; for pain syndromes, fever, etc. both alone and together with antibacterial agents; to control inflammatory processes secondary to the diseases of the musculoskeletal system; to relieve pain syndrome (of various etiology) in horses, cattle and pigs.

Due to Flunex applied, the recovery period can be reduced by 36 hours, with positive dynamics observed 18 hours earlier compared with a monotherapy.

Due to Flunex applied, the recovery period in the case of suppurative and catarrhal mastitis can be reduced by 12 hours, with positive dynamics observed 9 hours earlier compared with a monotherapy.

Due to Flunex applied, the intensity of symptoms can be reduced in 7 hours, which is 17 hours less than that occurred when a monotherapy is used. Thus, the condition of the animal is quickly improved and the weight gain is stable.

Due to Flunex applied, the recovery period can be reduced by 24 hours compared to a monotherapy, and the temperature is normalized after 30 minutes

Video

Dosage and route of administration

Animal species	Indications	Route of administration	Dosage	Frequency of administration	Treatment regimen
Cattle	Respiratory disease Acute mastitis Other diseases	Intramuscularly Intravenously	2 mL/45 kg	Once a day	Maximum 5 days
Horses	Musculoskeletal system disorders	Intravenously	1 mL/45 kg	Once a day	Maximum 5 days
	Relief from pain syndrome at colic		1 mL/45 kg	Once	If required, repeat administration at the same dose in 24 hours
	Endotoxemia, septic shock, and other pathologies associated with circulatory disorders in the digestive tract		0,2 mL/ 45 kg	Every 6 to 8 hours	Maximum 5 injections
Pigs	MMA syndrome Respiratory disease	Intramuscularly	2 mL/45 kg	Once

Restrictions

CONTRAINDICATIONS

Hypersensitivity of an animal to the drug components. Avoid using the drug in animals suffering from renal, liver, heart failure, or hypovolemia (except for endotoxemia or septic shock).

Intra-arterial administration of Flunex to animals is prohibited

Due to the increased risk of a painful reaction, avoid administering more than 5 mL of the solution in large animals and 2.5 mLin small animals to a single injection site.

Avoid using the drug in pregnant females, animals younger than 1.5 months, or in pigs with the body weight of less than 6 kg.

Avoid using Flunex concurrently with other anti-inflammatory drugs or nephrotoxic agents.

RESTRICTIONS

After the treatment with Flunex, cattle can be slaughtered for human consumption at least 8 days after the drug was administered intravenously for the last time and 35 days after the drug was administered intramuscularly; horses - at least 8 days; pigs - at least 24 days after the last administration of the drug.

In the case of forced slaughter of animals before the established deadlines, the meat can be used for feeding fur-bearing animals.

The milk, obtained from the treated milked animals, may be used for human consumption no earlier than 60 hours after the last dose of Flunex was administered. Taken before expiration of the restriction period, the milk can be used for animal feeding after boiling.

SHELF LIFE

3 years from the date of manufacture; after first opening - 28 days.

Please note: The information given on this page is for an informative purpose only. Product characteristics, packaging, label design and overall appearance may vary in different regions. Contact our representatives for more information.

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