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PHARMACOLOGY (TAKE DOWN NOTES) TO REVIEW!

 Pharmaceutics – break down of the capsule 1. Medications to prevent heat, cure –


* Pinocytosis – passive, active pharmacotherapy
 Kinetics – absorption, distribution, 2. Effects of the body on the drugs –
metabolism, excretion pharmacokinetics
 Pharmacodynamics – action of drug on the 3. Known as undesirable effects – toxicology
body 4. Losartan, lowers bp – pharmacokinetics
 Passive – diffusion (has high and low 5. Receptor – pharmacodynamics
concentration) 6. Stomach ulcer, otc mefenamic acid –
*blood cloth – example of diffusion, pharmacokinetics
high concentration 7. Oral has higher drugs – false
 Active – need enzymes, proteins 8. Infants drug metabolism does not happen
 Kinocytosis – inside the cell, cells carry the due to immature liver function – false
drug into membrane 9. Actions of the drug on the body –
 Distribution – the drugs become available pharmacodynamics
to body fluid 10. Physical nature of drugs –
*when blood decrease, the distribution pharmacokinetics
of blood will be delayed 11. Enantiomers – disarrange
 Metabolism – the body inactivates or 12. Response is too small for clinical benefits –
biotransform the drugs ; 12 hrs/ 6 hrs (half minimum effect concentration
life) until it eliminates 13. Drug with material design to dissolve in the
 Elimination – 4.5 – 8 normal urine PH intestine – enteric coated preparation
14. Sublingual need – 30 mins, then re-assess
 Creatinine clearance – before giving toxic
15. 3 existing vascular – placental, blood-brain
drugs
barriers,
Normal GFR – 90 above; increased
16. Consideration – age, sex, nutritional status
creatinine level in blood and urine
17. Highest drug concentration – peak level
 Pharmacodynamics – study of the drugs
18. Withdraws blood sample – half life
Drug response:
19. Withdraw before next administration –
 Primary – desirable effect on
through
the patient
20. Adverse reaction – unexpected
 Secondary effect – can be
21. Drug interaction – drug-drug, drug-
desirable or not
food/beverage, drug-condition interaction
 Chemical – composition of molecular
22. The greater the agent, the lower the
 Generic – lower case letters on drugs
concentration – false
packaging
23. Some drugs are eliminated without
 Trade name – capslock/ bold letter
undergoing metabolism – false
24. A drug maybe eliminated without
NATURE OF DRUGS
undergoing metabolism – false
 Sterile – disarranged molecule
25. Herbal produced are safer than medical
 Enantiomers – mirror life/image drugs – false
 Onset – minimum effect of drug 26. After taking long lasting insulin, the
 Peak – maximum patient’s blood pressure lowers after 20
 Duration of action – after observing onset mins – pharmacodynamics
effect until least 27. Partial agonist have lower maximal – true
 Half life (peak concentration) – withdraw 28. Drugs with zero order eliminations have
blood during peak time before constant half life – false
administering next dose 29. Pharmacognosy is the study of drug made
 1st dose – withdraw from natural substances/sources – true
 Through – withdraw before 2nd dose (?) 30. When a drug is distributed in the body, it
 Enteric – coated (dissolves at intestine, means that it has reached the tissues and
should not crush the drug) cells – true
 Sustained – release 31. About 12% - pharmacokinetics
 Distribution of drugs – delayed 32. Drugs can turned on the body’s
 Absorption – delayed if the patient is too physiological functions – true
young or too old because of gastric
contents QUIZ 2
 Dose adjustment – in pain Enumeration: component required on all labels

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