Pharmacology - Quiz#1 Material

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1. What does the term 'Generic Name' refer to in the context of pharmaceuticals?

Explanation

The generic name refers to the common or general name of a drug, which can be used by any manufacturer to produce the medication. It is distinct from the brand name, which is owned and registered by a specific pharmaceutical company. Additionally, the generic name does not indicate the specific chemical composition of the drug, nor does it relate to the company that manufactures it.

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About This Quiz
Pharmacology - Quiz#1 Material - Quiz

Introduction to Pharmacology
QUIZ 1 material
Ch 10, 11, 12, 13, 14

2. What does pharmacokinetics refer to?

Explanation

Pharmacokinetics specifically focuses on how the body processes a drug through absorption, distribution, metabolism, and excretion, rather than drug production, interactions with food, or pricing/marketing strategies.

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3. What field of study focuses on identifying and studying poisons?

Explanation

Toxicology is the science that specifically deals with poisons and their effects on living organisms. Geology focuses on the Earth's physical structure and substance, meteorology studies the atmosphere and weather patterns, and psychology is the study of the mind and behavior.

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4. What is pharmacology?

Explanation

Pharmacology is the science of drugs including their origin, composition, pharmacokinetics, therapeutic use, and toxicology. It involves understanding how drugs interact with living organisms to produce a desired effect.

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5. What is meant by the term 'minimum dose'?

Explanation

The term 'minimum dose' refers to the lowest amount of a medication or substance that is needed to achieve the desired effect, without taking more than necessary. This ensures that the individual is taking the least amount possible while still benefiting from the treatment.

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6. What is meant by the term 'maximum dose'?

Explanation

The maximum dose refers to the highest amount of a substance that can be consumed without causing harmful or toxic effects on the individual. It is essential in determining the safe limits of drug or substance administration.

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7. What is a loading dose?

Explanation

A loading dose is administered initially to rapidly achieve therapeutic levels in the bloodstream before transitioning to a maintenance dose for ongoing therapy.

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8. What is meant by maintenance dose?

Explanation

A maintenance dose is the amount of a drug that is required to keep the desired therapeutic effect over time. It is not the initial dose used to start treatment, the maximum dose allowed, or the dose needed for a cure or to avoid side effects.

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9. What is the definition of a lethal dose?

Explanation

A lethal dose is a dose of a substance that causes death to the organism that receives it. It is a term commonly used in toxicology and pharmacology.

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10. What does the term 'therapeutic dose' refer to?

Explanation

A therapeutic dose refers to the range of dosage that is needed to maintain the desired response safely, ensuring that the benefits of the medication outweigh any potential risks.

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11. What does the FDA (Food and Drug Administration) do?

Explanation

The FDA is responsible for ensuring the safety and quality of food, drugs, and cosmetics through regulations and laws.

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12. What is misbranding?

Explanation

Misbranding refers to the situation where the name on the label of a drug does not match the actual contents of the drug. This can lead to confusion and potential harm to consumers.

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13. What does tolerance refer to in the context of drug use?

Explanation

Tolerance occurs when the body adapts to a drug, causing the individual to need higher doses to achieve the same initial effects.

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14. What are the types of Drug References?

Explanation

Primary drug references consist of medical and professional journals, while secondary drug references provide factual and approved information on drugs (e.g., PDR, USP up to date by 1 year). Tertiary drug references typically include textbooks, although they are not as up to date as primary and secondary references.

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15. What is In Vitro Testing?

Explanation

In Vitro Testing specifically refers to testing conducted in controlled laboratory conditions using test tubes or equipment, rather than on live animals, in a simulated environment, or through computational models.

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16. What is In Vivo Testing?

Explanation

In Vivo Testing refers to experiments or trials that are conducted in living organisms such as animals or humans to observe the effects of substances or treatments. It is different from in vitro testing which is done in controlled laboratory settings without involving living organisms. In Vivo Testing is crucial as it allows researchers to study the biological processes, effects, and potential risks of new compounds or drugs within a living system before they can be used on humans.

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17. What are the stages in testing a new drug?

Explanation

The correct answer is 3 phases - phases one, two, and three - with each phase focusing on a specific aspect of drug testing.

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18. What is the medical term 'Enteral' refer to?

Explanation

Enteral refers to the administration of medication or nutrients via the oral route, while IV, IM, and SQ refer to administration methods involving injection into veins, muscles, and under the skin respectively.

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19. What is the definition of parenteral?

Explanation

Parenteral refers to any route of administration other than oral. This includes injections given intravenously (IV), intramuscularly (IM), or topically.

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20. What are examples of oral drug dosage forms?

Explanation

Oral drug dosage forms are medications that are taken by mouth. Examples include tablets, capsules, and various liquid forms such as suspensions, elixirs, and syrups. In contrast, injections, patches, and creams are not considered oral dosage forms.

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21. What are examples of topical drug dosage forms?

Explanation

Topical drug dosage forms are applied to the skin for localized effects, not taken orally, intravenously, or rectally.

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22. What are examples of parenteral dosage forms?

Explanation

Parenteral dosage forms are administered by injections either directly into a vein using a syringe, or through an IV infusion or drip. Tablets, creams, and suppositories are not considered parenteral dosage forms as they are administered through oral, topical, or rectal routes respectively.

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23. What are Drug Interactions?

Explanation

Drug Interactions can occur when multiple drugs are used simultaneously, or when drugs interact with specific foods or other substances. It is not limited to just one drug, can involve different types of drugs, and is not exclusive to herbal supplements.

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24. What does DEA stand for?

Explanation

DEA stands for Drug Enforcement Agency and is responsible for enforcing the controlled substances laws and regulations in the United States.

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25. What is the purpose of an IND (Investigating New Drugs)?

Explanation

An Investigational New Drug (IND) application is submitted to the FDA by a drug company after preliminary animal studies have been conducted to gather data on the safety and efficacy of a new drug. This application must be approved by the FDA before clinical trials can begin in humans.

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26. What is the length of time for Drug Patents?

Explanation

Drug patents typically last for 20 years from the date of filing, but due to the lengthy approval process from regulatory agencies, the effective patent life is often around 17 years.

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27. How many Schedules of Controlled Substances are there and what is their order of severity?

Explanation

Controlled substances are classified into 5 schedules based on their potential for abuse and dependency. The correct order of severity is CI to CV, with CI having the highest potential for abuse and CV having the lowest.

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28. How does absorption occur in the human body?

Explanation

Absorption primarily occurs at the mucosa, where nutrients pass through the cell membranes and into the bloodstream. Skin absorption is more relevant for topical applications, while the esophagus and stomach are primarily involved in the digestion process.

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What does the term 'Generic Name' refer to in the context of...
What does pharmacokinetics refer to?
What field of study focuses on identifying and studying poisons?
What is pharmacology?
What is meant by the term 'minimum dose'?
What is meant by the term 'maximum dose'?
What is a loading dose?
What is meant by maintenance dose?
What is the definition of a lethal dose?
What does the term 'therapeutic dose' refer to?
What does the FDA (Food and Drug Administration) do?
What is misbranding?
What does tolerance refer to in the context of drug use?
What are the types of Drug References?
What is In Vitro Testing?
What is In Vivo Testing?
What are the stages in testing a new drug?
What is the medical term 'Enteral' refer to?
What is the definition of parenteral?
What are examples of oral drug dosage forms?
What are examples of topical drug dosage forms?
What are examples of parenteral dosage forms?
What are Drug Interactions?
What does DEA stand for?
What is the purpose of an IND (Investigating New Drugs)?
What is the length of time for Drug Patents?
How many Schedules of Controlled Substances are there and what is...
How does absorption occur in the human body?
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