What percentage of prescription medications are spent in these settings? Match the items. – a. b. c. d. Hospitals a. 58.3%

What percentage of prescription medications are spent in these settings? Match the items.

– a. b. c. d. Hospitals
a. 58.3%
– a. b. c. d. Physician and clinical service
b. 26.3%
– a. b. c. d. Nursing homes
c. 3.9%
– a. b. c. d. Home health
d. 11.5%
Choose the states with the largest percentage of population over age 65.
a. Massachusetts
b. West Virginia
c. South Carolina
d. California
e. Vermont
f. Ohio
g. North Carolina
h. Montana
In the U.S., the states have authority to regulate for the protection of public health and to provide health services is based on____________.
a. police power
b. constitutional amendment power
c. false, they do not have the authority to tell the public what to do
d. legislated power
Section 351 of the Public Health Service (PHS) Act as amended by the Biologics Price Competition and Innovation Act of 2009 (otherwise known as the BPCI Act) defines a biological product as________________________________________.
a. any prescription medication used to treat disease or illness in human beings.
b. a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, or analogous product, … applicable to the prevention, treatment, or cure of a disease or condition of human beings.
c. any plant-based medical treatment capable of producing cellular genetic variations leading to a healthful balance of the oxidative phosphorylation cycle.
d. any mRNA based delivery system for communicable disease that functions as a vaccination
Which authority is responsible for each healthcare need?
– a. b. Medicaid
a. State Control

– a. b. Mental Health

b. Federal Government Control

– a. b. Welfare/Food Stamps/Other income-based assistance

– a. b. Public Health (local)

– a. b. Medicare
– a. b. Environmental Protection Agency (EPA)
– a. b. Department of Defense (DOD)
– a. b. Centers for Disease Control (CDC)
Section 351 of the Public Health Service (PHS) Act as amended by the Biologics Price Competition and Innovation Act of 2009 (otherwise known as the BPCI Act) defines a biological product as________________________________________.
a. any prescription medication used to treat disease or illness in human beings.
b. a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, or analogous product, … applicable to the prevention, treatment, or cure of a disease or condition of human beings.
c. any plant-based medical treatment capable of producing cellular genetic variations leading to a healthful balance of the oxidative phosphorylation cycle.
d. any mRNA based delivery system for communicable disease that functions as a vaccination
Medical supplies differ from medical equipment in that supplies are one-time use and equipment can be used multiple times.
True
False
Testing for new pharmaceuticals is a very rigorous process and is strictly controlled by the FDA. Place each of the 7 required steps in order.
– 1. 2. 3. 4. 5. 6. 7.
Within 60 days FDA to decide/If the FDA files the NDA, an FDA review team for drug’s safety and effectiveness

– 1. 2. 3. 4. 5. 6. 7.
The pre-NDA period, FDA/drug sponsors meet/Submission of an NDA

– 1. 2. 3. 4. 5. 6. 7.
Phase 1 studies (typically involve 20-80 people)

– 1. 2. 3. 4. 5. 6. 7.
The FDA reviews labeling and manufacturing facilities and approve the application letter

– 1. 2. 3. 4. 5. 6. 7.
Preclinical (animal) testing/An investigational NDA (IND)

– 1. 2. 3. 4. 5. 6. 7.
Phase 3 studies (typically involve several hundred to about 3,000 people)

– 1. 2. 3. 4. 5. 6. 7.
Phase 2 studies (typically involve a few dozen to about 300 people)
this quizze, there is no reference