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NU578 Unit 1 Exam Questions and Answers All Correct CA$17.96   Add to cart

Exam (elaborations)

NU578 Unit 1 Exam Questions and Answers All Correct

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NU578 Unit 1 Exam Questions and Answers All Correct Factors affecting absorption - Answer- rate of dissolution surface area blood flow lipid solubility pH partitioning Barriers to PO absorption - Answer- Epithelial cells Capillary walls Sometimes p-glycoprotein Factors affecting P...

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  • September 25, 2024
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NU578 Unit 1 Exam Questions and
Answers All Correct

Factors affecting absorption - Answer- rate of dissolution
surface area
blood flow
lipid solubility
pH partitioning

Barriers to PO absorption - Answer- Epithelial cells
Capillary walls

Sometimes p-glycoprotein

Factors affecting PO absorption - Answer- Solubility & stability
Gastric.intestinal pH
Gastric emptying time
Food in the gut
Coadministration of other drugs
Coatings on the drug

Abscesses & tumors - Answer- Low regional blood flow affects therapy

(Lack of blood flow inhibits drug delivery to the site.
Abscess - Pus-filled pockets don't have internal blood vessels
Solid tumors - have a limited blood supply)

Idiosyncratic effect - Answer- an uncommon drug response resulting from a genetic
predisposition

ex: G6PD deficiency

Paradoxical effect - Answer- a response to a medication that is the opposite of what is
expected

iatrogenic disease - Answer- disease produced by drugs

physical dependence - Answer- a state in which the body has adapted to drug exposure
in such a way that an abstinence syndrome will result if drug use is discontinued

,carcinogenic effect - Answer- the ability of certain medications and environmental
chemicals to cause cancers

teratogenic effect - Answer- causal relationship between the drug use of a mother and
congenital abnormalities (congenital defect)

Hepatotoxic drugs - Answer- as some drugs undergo metabolism by the liver, they are
converted to toxic products that can injure liver cells

LFTs to assess liver function and hepatotoxicity - Answer- AST & ALT

QT Interval Drugs - Answer- the ability of some medications to prolong the QT interval
on the electrocardiogram, thereby creating a risk of serious dysrhythmias

Patient at risk for adverse effects of QT drugs - Answer- - Older adults
- Patients with dysrhythmias
- Low K and Mag
- Women
- Current use of other QT drugs

pharmacodynamic tolerance - Answer- adaptive changes in systems affected by the
drug so that the response to a given concentration of drug is reduced

Schedule I - Answer- Drugs in this schedule have no accepted medical use in the
United States and have a high abuse potential.

Examples are heroin, marijuana, LSD, peyote, etc.

Schedule II - Answer- Drugs in this schedule have a high abuse potential with severe
psychic or physical dependence liability. Included are certain narcotic analgesics,
stimulants, and depressant drugs.

Examples are opium, morphine, codeine, hydromorphone, methadone, meperidine,
oxycodone, anileridine, cocaine, amphetamine, methamphetamine, phenmetrazine,
methylphenidate, amobarbital, pentobarbital, secobarbital, methaqualone, and
phencyclidine.

Schedule III - Answer- Drugs in this schedule have an abuse potential less than those in
Schedules I and II and include compounds containing limited quantities of certain
narcotic analgesic drugs, and other drugs such as barbiturates, glutethimide,
methyprylon, and chlorphentemine.

Any suppository dosage form containing amobarbital, secobarbital, or pentobarbital is in
this schedule.

, Schedule IV - Answer- Drugs in this schedule have an abuse potential less than those
listed in Schedule III and include such drugs as barbital, phenobarbital, chloral hydrate,
ethchlorvynol, meprobabmate, chlordizepoxide, diazepam, oxazepam, chloroazepate,
flurazepam, etc.

Schedule V - Answer- Drugs in this schedule have an abuse potential less than those
listed in Schedule IV and consist primarily of preparations containing limited quantities
of certain narcotic analgesic drugs used for antitussive and antidiarrheal purposes.

Absorption - Answer- Process of drug movement from its site of administration into the
blood

Most common mechanism for drug absorption - Answer- passive diffusion

First-pass effect
(presystemic metabolism) - Answer- Rapid hepatic inactivation of certain oral drugs

drug is metabolized (chemically altered) as it passes through either 1) gut wall, and 2)
liver.

Distribution - Answer- drug movement from the blood to the interstitial space of tissues
and from there into cells

Barriers to distribution - Answer- - Blood brain barrier
- Placenta

Physiologic Factors Affecting Distribution - Answer- - Perfusion
- Binding of drug to plasma protein
- Specialized Distribution Barriers

Albumin - Answer- Binds acidic drugs

Protein (albumin) binding - Answer- Prevents bound drug molecules from leaving the
bloodstream

Prolongs the distribution phase (Increases half-life)

alpha-1 acid glycoprotein - Answer- Binds basic drugs

Reservoir effect - Answer-

Blood-Brain Barrier (BBB) - Answer- no intercellular pores between brain capillary
endothelial membranes due to the presence of tight junctions between cells

To gain access to the brain from the capillaries, drugs must - Answer- 1) diffuse across
cells (lipid-soluble,

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