Full Exam Prep for:
Chapter 1: Introduction to Respiratory
Care Pharmacology,
Chapter 2: pharmacology this one,
RAU's Respiratory Care Pharmacology
Chapter 3: Key Terms
** Expert-Verified Explanation
** Questions with Verified Answer
** New Edition | 2026-2027 Updated
** 100% Guaranteed Pass
** 100% Correct Answers | Graded A+
,What is the definition of Drugs? Chemicals that interact with an organism to alter it's function/. medication that
causes a change in the body (pp)
What is the definition of Pharmacology? The study of drugs (chemicals), including their origins, properties, and
interactions with living organisms. (pp)
pharmacognasy identification of drugs plant or animal (pp)
pharmacogenetics interrelationship of genetic differences and drug effects (pp)
What is the definition of Therapeutics? The art of treating disease with drugs. (power point*)
What is the definition of Toxicology? The study of toxic substances and their pharmacologic actions, including
antidotes and poison control.(pp)
A drug has 5 names. What are they? Chemical Name, Code Name, Generic Name, Official Name and Trade Name.
What is the "Chemical Name" of a drug described as? The drugs chemical structure. (PP)
What is the "Code Name" of a drug described as? experimental drug name (pp) /The name assigned by the manufacturer.
What is the "Generic Name"/ non-proprietary name of a Therapeutic name which can be marked (power point*)The name assigned by
drug described as? the USAN Council.
What is the "Official Name" of a drug described as? same name as The generic name. (pp)
What is the "Trade Name" of a drug described as? The brand name./ or proprietary name (power point*) like advil tylenol
What is the standard dose for Albuterol? 2.5 mg.
What is considered the "unbiased" or "official standard United States Pharmacopeia-National Formulary. (this is the end all) (usp) (pp)
according to the FDA" book source on drug information?
What is considered the "biased" source of drug Physician's Desk Reference. (PDR) (pp)
information that is prepared by the manufacturer?
What are the different sources of drugs? Animals, plants, and minerals. And synthesis (pp)
, What is the most common source of drug preparation? Chemical synthesis. (pp)
Synthesis made to focus on the good and last longer save the animals
The process for drug approval in the U.S. is described Lengthy, expensive, and involves multiple phases.
as?
U.S approval process fda 15 years 800 million dollars chemical id, animal study's, investigational approval
human studies new drug application new drug 6 months probation (pp)
patents exclusivity patents are granted by the patent and trade marked office expires 20 years from
the date filled
exclusivity is exclusive marking righs by the fda orphan drug (ODE) New chemical (NCE) prediatric exclusivily (PED) (pp)
chemical pharmaceutial standing classification system name chemical entity, new salt form, new combination, generic drug, new
indication (pp)
therapeutic potential A/AA/B/C
WHAT is the therapeutic potential of/ A SEE MORE significant therapeutic gain
WHAT is the therapeutic potential of/AA significant therapeutic gain BUT FAsT TRACKED FOR THINGS LIKE ADIS
WHAT is the therapeutic potential of/ B MODEST therapeutic gain
WHAT is the therapeutic potential of/ C LITTLE or NO therapeutic gain
The chemical process of drug approval in the U.S. does Isolates and identifies.
what with the chemicals?
The drug process in the U.S. in done on what species? Animal testing.
How many phases are involved in the Investigational 3.
New Drug approval?
Phase 1 of the Investigational New Drug approval is A small number of healthy subjects.
done on?
Chapter 1: Introduction to Respiratory
Care Pharmacology,
Chapter 2: pharmacology this one,
RAU's Respiratory Care Pharmacology
Chapter 3: Key Terms
** Expert-Verified Explanation
** Questions with Verified Answer
** New Edition | 2026-2027 Updated
** 100% Guaranteed Pass
** 100% Correct Answers | Graded A+
,What is the definition of Drugs? Chemicals that interact with an organism to alter it's function/. medication that
causes a change in the body (pp)
What is the definition of Pharmacology? The study of drugs (chemicals), including their origins, properties, and
interactions with living organisms. (pp)
pharmacognasy identification of drugs plant or animal (pp)
pharmacogenetics interrelationship of genetic differences and drug effects (pp)
What is the definition of Therapeutics? The art of treating disease with drugs. (power point*)
What is the definition of Toxicology? The study of toxic substances and their pharmacologic actions, including
antidotes and poison control.(pp)
A drug has 5 names. What are they? Chemical Name, Code Name, Generic Name, Official Name and Trade Name.
What is the "Chemical Name" of a drug described as? The drugs chemical structure. (PP)
What is the "Code Name" of a drug described as? experimental drug name (pp) /The name assigned by the manufacturer.
What is the "Generic Name"/ non-proprietary name of a Therapeutic name which can be marked (power point*)The name assigned by
drug described as? the USAN Council.
What is the "Official Name" of a drug described as? same name as The generic name. (pp)
What is the "Trade Name" of a drug described as? The brand name./ or proprietary name (power point*) like advil tylenol
What is the standard dose for Albuterol? 2.5 mg.
What is considered the "unbiased" or "official standard United States Pharmacopeia-National Formulary. (this is the end all) (usp) (pp)
according to the FDA" book source on drug information?
What is considered the "biased" source of drug Physician's Desk Reference. (PDR) (pp)
information that is prepared by the manufacturer?
What are the different sources of drugs? Animals, plants, and minerals. And synthesis (pp)
, What is the most common source of drug preparation? Chemical synthesis. (pp)
Synthesis made to focus on the good and last longer save the animals
The process for drug approval in the U.S. is described Lengthy, expensive, and involves multiple phases.
as?
U.S approval process fda 15 years 800 million dollars chemical id, animal study's, investigational approval
human studies new drug application new drug 6 months probation (pp)
patents exclusivity patents are granted by the patent and trade marked office expires 20 years from
the date filled
exclusivity is exclusive marking righs by the fda orphan drug (ODE) New chemical (NCE) prediatric exclusivily (PED) (pp)
chemical pharmaceutial standing classification system name chemical entity, new salt form, new combination, generic drug, new
indication (pp)
therapeutic potential A/AA/B/C
WHAT is the therapeutic potential of/ A SEE MORE significant therapeutic gain
WHAT is the therapeutic potential of/AA significant therapeutic gain BUT FAsT TRACKED FOR THINGS LIKE ADIS
WHAT is the therapeutic potential of/ B MODEST therapeutic gain
WHAT is the therapeutic potential of/ C LITTLE or NO therapeutic gain
The chemical process of drug approval in the U.S. does Isolates and identifies.
what with the chemicals?
The drug process in the U.S. in done on what species? Animal testing.
How many phases are involved in the Investigational 3.
New Drug approval?
Phase 1 of the Investigational New Drug approval is A small number of healthy subjects.
done on?
