Top best answers to the question «Under what circumstances can a drug be used extra-label in a companion animal»
Extra-label drug use in food animals is permitted only by or under the supervision of a veterinarian, is allowed only for therapeutic purposes (ie, the animal's health is suffering or threatened), is not allowed when the drug is administered in feed, is not permitted if it results in violative food residues or any ...
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The purpose of FDA’s requirements for extra-label drug use in animals is to limit this use to situations where an animal’s health is threatened or where the animal may suffer or die without ...
Q: What situations justify use of an extra label drug? RS: Extra label use is limited to circumstances when the health of an animal is threatened, or suffering or death may result from failure to treat. 2. There are additional conditions: There must be no animal drug already approved for the disease or condition you want to treat.
In 1994, Congress passed a law that allows veterinarians to prescribe approved human and animal drugs for extra-label uses in animals under specified conditions.
Extra-label use is limited to circumstances when the health of an animal is threatened, or suffering or death may result from failure to treat. This means that extra-label use to enhance production is prohibited. Extra-label use of drugs may be considered by food animal veterinarians only when:
A vet or pharmacist may supply POM-V products or products for use under the cascade (a provision in the VMR that allows a vet to prescribe medicines that would not otherwise be permitted) to non ...
Where there is no suitable veterinary medicine authorised in your territory for the specific condition in the animal being treated, to avoid unacceptable suffering, you are permitted to use your ...
Labels of drugs for human use in dosage form include information for a contact person in Canada (e.g. , telephone number, email address, website address, postal address or other information that allows communication) and; A statement that harms associated with the use of the drug can be reported to that person.
on every product label: “Do not use on animals under XX weeks of age.” The minimum age may not be less than 12 weeks unless acceptable companion animal safety and efficacy data are submitted to the PMRA to support the product’s use on younger animals. 2.5 Sick, Aged, Pregnant or Nursing Animals and Animals Under Drug or Pesticide Treatment
These guidelines should be used as a companion document to the official version of the ICD-10-CM as published on the NCHS website. The ICD-10-CM is a morbidity classification published by the United States for classifying diagnoses and reason for visits in all health care settings. The
§483.60(d) Labeling of Drugs and Biologicals Drugs and biologicals used in the facility must be labeled in accordance with currently accepted professional principles, and include the appropriate accessory and cautionary instructions, and the expiration date when applicable. §483.60(e) Storage of Drugs and Biologicals