Unit 1 Flashcards

1
Q

Define pharmacotherapeutics.

A

Pharmacotherapeutics: the administration of drugs for the purpose of of disease prevention or treatment and the relief of suffering.

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2
Q

Differ between dugs and medications.

A

Drugs: chemical agent capable of producing biological response
Medication: used medically, synthesized in a lab

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3
Q

Define biologics.

A

Biologics: agents that are naturally produced in animal cells (e.g.: hormones, antibodies)

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4
Q

Define natural health products.

A

NHPs: naturally occurring from many sources, used to support health and well-being

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5
Q

What are the advantages of prescription?

A

Qualified health care provider will prescribe drug specific to the client; client will be more informed about drug.

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6
Q

What are the advantages and disadvantages of OTC drugs?

A

Advantages: convenient, cheaper
Disadvantages: less specificity, adverse effects if not used properly

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7
Q

What 5 things must a drug label include?

A

1) Generic drug name
2) DIN #
3) Lot number
4) Expiry date
5) Ingredients

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8
Q

What is the purpose of the preclinical investigation with prescription drug approval?

A

Preclinical investigations predict whether the drug will cause harm to humans by testing on animals and on cells cultured in labs.

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9
Q

Outline the 3 phases of clinical trials.

A

Phase I: tests on healthy volunteers to assess drug absorption, metabolism, and excretion
Phase II: tests on volunteers with target disease to determine proper dosage and side effects
Phase III: double blind study

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10
Q

What is the purpose of post approval surveillance and regulation?

A

Post approval surveillance and regulation monitors for adverse effects not demonstrated in clinical trials.

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11
Q

Differentiate between therapeutic and pharmacological classification.

A

Therapeutic: organizes drugs based on their therapeutic usefulness in treating particular diseases; states what the drug does
Pharmacological: organizes drugs based on how they work at molecular, tissue, and body system level; addresses mechanisms of action

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12
Q

Define bioavailability.

A

Bioavailability: amount of drug that physiologically available to reach its target cells and produce its effect

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