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Which regulatory agency would initiate a Class II medication recall?

Joe Ford

Which regulatory agency would initiate a Class II medication recall?

PTCB Pratice Test 1

Question Answer
What is C C X L equal to? 240
Mrs. McTarnahan is picking up an order of drug “T” #100 tablets which costs her $122.00. While you’re ringing up her order, she asks “How much does each tablet cost?” $1.22
Which regulatory agency would initiate a Class II recall on a prescription drug? FDA

What is the drug importation Act?

The bill requires the Food and Drug Administration (FDA) to promulgate regulations within 180 days permitting wholesalers, pharmacies, and individuals to import certain prescription drugs from Canada. After two years, The FDA, may permit the importation of prescription drugs from other countries.

What is Class II recall?

Class II Recall: A Class II recall means the use of a violative product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. Examples of Class II recalls include botulinum potential and Norovirus contamination in seafood.

What is a Class II drug recall?

Class II recall: a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Who can administer medication in a care establishment?

If the care home is registered to provide nursing care then it should be the medical practitioner or registered nurse who administers medicines.

  • Appropriate staff members should be suitably trained in the administration of medicines and the homes policy should state how frequently training updates are accessed.

    • Can CRNA write prescriptions?

    Advanced practice nurses include titles such as a certified nurse practitioner (CNP), certified nurse-midwife (CNM), certified registered nurse anesthetist (CRNA), or clinical nurse specialist (CNS). As a rule, a nurse holding one of these credentials can independently prescribe drugs listed as schedule 3 or above.

    Which type of recall is suggested by drug regulatory bodies?

    (b) Statutory recall: These are recalls mandated by drug regulatory bodies at Central or State levels for one of the following reasons: 1. The product violates the law – for example, it is not of standard quality.