Buparvaquone Injection (box of 1 vial)
Buparvaquone Injection (box of 1 vial)
*Packaging color and/or animals may vary according to distribution region.

Buparvaquone Injection

BuvaCare™
Buparvaquone Injection is an antiparasitic medicine that treats and prevents tick-transmitted theileriosis in cattle. This veterinary injection is manufactured according to the highest production standards by AdvaCare Pharma in one of its GMP/ISO-certified facilities.

Dosage

Packaging

What is Buparvaquone?

Therapeutic Class:
Target Species:

Active Ingredients: Buparvaquone

Buparvaquone Injection is a drug used to treat and prevent tick-transmitted theileriosis in cows. It is indicated for infections caused by the parasite Theileria parva, including east coast fever, corridor disease, and Zimbabwe theileriosis. It is also effective against tropical theileriosis caused by T. annulate.

Buparvaquone is effective during the schizonts and piroplasms stages of the disease. It also can be used during the incubation period.

Buparvaquone is classified as a second-generation hydroxynaphthoquinone. It is an antiprotozoal agent that is related to the drug atovaquone. Though the exact mechanism of action has not been identified, it is thought to work by blocking the respiratory chain within the parasite.

It is important to note that this drug is for veterinary purposes only. It should be prescribed by a veterinary doctor or animal care specialist for an animal.

Buparvaquone Injection is produced by AdvaCare Pharma, a pharmaceutical company specializing in global exportation. This medication is part of our comprehensive catalog of veterinary supplies which are available for distribution. Our manufacturing factories are located in China, India, and the USA.

Why are we a trusted Buparvaquone manufacturer?

Buparvaquone Injection is manufactured and globally distributed by AdvaCare Pharma, a leading manufacturer of veterinary injections in the pharmaceutical industry. We have been committed to distributing high-quality, GMP-certified veterinary medications for the global market for the past 20 years. To ensure that our products meet and surpass our distributors' requirements, we carry out routine internal and third-party facility audits.

Uses

What is Buparvaquone used for?

It's used to treat or prevent tick-transmitted theileriosis caused by Theileria parva or T. annulate, including the diseases:

It is effective against both the schizont and piroplasm stages of the parasite.

What animals can be treated with Buparvaquone Injection?

This medicine is recommended for use in cows.

How is Buparvaquone Injection used?

This medication has been manufactured as a liquid, which is packaged in a vial. It is intended to be administered by intramuscular injection.

How should Buparvaquone Injection be stored?

This medication should be stored in a dark, dry location between 15-25°C. The vial should be sealed tightly when not used.

What are the withdrawal times for Buparvaquone Injection?

The withdrawal period for meat is 42 days. For milk, the withdrawal period is 48 hours.

Dosage

How much Buparvaquone should be given to cattle?

The usual dose is 1ml per 20kg of body weight, given as single dose. Treatment may be repeated 48-72 hours later if necessary. This injection is typically administered into the neck muscles.

Side Effects

As with all pharmaceuticals, some unwanted effects can occur from the use of Buparvaquone Injection.

Localized reactions and pain at the injection site are a common side effect. Serious side effects may include signs of an allergic reaction (skin rash, fever, facial swelling, or difficulty breathing).

For a comprehensive list of all possible side effects of this medication, consult a veterinary physician.

Precautions

Do NOT use Buparvaquone Injection in animals that: • have a known allergy or hypersensitivity to any of the ingredients.

Due to the immunosuppressive effects of this medicine, vaccines should be delayed until after the animal has fully recovered from illness.

Do not administer this injection through the subcutaneous or intravenous routes.

*Regulatory compliance may vary according to production standard, import requirements and/or manufacturing origin.

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