Inj.

Ketovet

Drug Class: Non Steroidal Anti-Inflammatory Drugs (NSAID)

Manufacturer: Techno Drugs Ltd.

Basic information

Generic Drug

Route of Administration

IM/IV

Strength / Concentration

100 mg/ml

Presentation and price

5 ml vial

Taka

10 ml vial

Taka

50 ml vial

Taka

Dose and dosage

Cattle

1ml/33kg body weight once daily for 3 days.

Buffalo

1ml/33kg body weight once daily for 3 days.

Goat

1ml/33kg body weight once daily for 3 days.

Sheep

1ml/33kg body weight once daily for 3 days.

Horse

1ml/33kg body weight once daily for 3 days.

Dog

1ml/33kg body weight once daily for 3 days.

Cat

1ml/33kg body weight once daily for 3 days.


Applications: Arthritis, Laminitis, Musculo skeletal system inflammation, Paresis, Post Surgical Pain, Injury, Inflammation, Ephemeral Fever

Do not administer to animals prone to GI ulcers. Do not administer with other ulcerogenic drugs such as corticosteroids.

Do not use with other NSAID


Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) used in people and animals. Like other NSAIDs, produces analgesic and anti-inflammatory effects by inhibiting the synthesis of prostaglandins. The enzyme inhibited by NSAID is the cyclo-oxygenase (COX) enzyme. The COX enzyme exists in two isoforms: COX-1 and COX-2. COX-1 is primarily responsible for synthesis of prostaglandins important for maintaining a healthy GI tract, renal function, platelet function, and other normal physiologic functions. COX-2 is induced and is responsible for synthesizing prostaglandins that are important mediators of pain, inflammation, and fever. However, it is known that there is some crossover of COX-1 and COX-2 effects in some situations, and COX-2 activity is important for some biological effects. Ketoprofen is a nonselective inhibitor of COX-1 and COX-2. There is weak evidence of its ability to inhibit lipoxygenase.

The following drug interactions have either been reported or are theoretical in humans or animals receiving ketoprofen and may be of significance in veterinary patients:
AMINOGLYCOSIDES (gentamicin, amikacin, etc.): Increased risk for nephrotoxicity
ANTICOAGULANTS (heparin, LMWH, warfarin): Increased risk for bleeding possible
ASPIRIN: When aspirin is used concurrently with ketoprofen, plasma levels of ketoprofen could decrease and an increased likelihood of GI adverse effects (blood loss) could occur. Concomitant administration of aspirin with ketoprofen cannot be recommended.
BISPHOSPHONATES (alendronate, etc.): May increase risk for GI ulceration
CORTICOSTEROIDS: Concomitant administration with NSAIDs may significantly increase the risks for GI adverse effects
CYCLOSPORINE: May increase risk for nephrotoxicity
FLUCONAZOLE: May increase NSAID levels
FUROSEMIDE: Ketoprofen may reduce the saluretic and diuretic effects of furosemide
HIGHLY PROTEIN BOUND DRUGS (e.g., phenytoin, valproic acid, oral anticoagulants, other antiinflammatory agents, salicylates, sulfonamides, and the sulfonylurea antidiabetic agents): Because ketoprofen is highly bound to plasma proteins (99%), it potentially could displace other highly bound drugs; increased serum levels and duration of actions may occur. Although these interactions are usually of little concern clinically, use together with caution.
METHOTREXATE: Serious toxicity has occurred when NSAIDs have been used concomitantly with methotrexate; use together with extreme caution.
PROBENECID: May cause a significant increase in serum levels and halflife of ketoprofen

All NSAIDs share the similar adverse effect of GI injury. The most common side effect is vomiting. GI ulceration is possible in some animals.

Not recommended during pregnancy.