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Review-Guide-in-Pharmacology-Prelim-Exam 2
Review-Guide-in-Pharmacology-Prelim-Exam 2
DRUG NAMES
1.Generic or Nonproprietary Name - name approved by the Medical or Pharmaceutical
Associations in the original country of manufacture and is adopted by all countries.
e.g. Paracetamol
2. Brand name or trade name - name given by the manufacturer of the drug for selling in the
market.
e.g. Adol or Panadol or Biogesic
3. Chemical name - name that describes the atomic or chemical structure
DRUG CLASSIFICATION
CHEMICAL STRUCTURES: pertains to the molecular arrangement of atoms in a molecule and the
chemical bonds that holds the atom together
MECHANISM OF ACTION (MOA): refers to the specific biochemical interaction through which
a drug substance produces its pharmacological effect such as an enzyme or receptor
MODE OF ACTION (MoA): describes a functional or anatomical change, resulting from the
exposure of a living organism to a substance
DRUG ACTIONS
Excipients - substances that will allow drug to take on particular size and shape and to enhance
drug dissolution.
Therapeutic effect - also referred as the DESIRED EFFECT (primary effect intended)
Side effect - also referred as the SECONDARY EFFECT (unintended effect) – Hold the
medications and inform the doctor.
ADVERSE EFFECT (severe side effects) - Hold the medications and inform the doctor.
Drug Toxicity - Deleterious effects of a drug resulting from over dosage, ingestion of external
use drug, and accumulation on the blood stream
Drug Allergy - immunologic reaction to drug
Drug Tolerance - exists in person with unusually low physiologic response to a drug compared
to other individuals. A person was given a maximum dose of a drug but experienced low
physiologic response/effect.
Repeated administration of the same drug decreases the effectiveness of that drug –
(increasing the dose)
PRINCIPLES OF DRUG ADMINISTRATION
PRACTICE GUIDELINES
If the RN is uncertain about the calculation, ask another nurse to double check
What you prepare, you administer
Correct Identification of patient – check ID band, ask the patient his name, compare in
the patients chart and ID band.
Observe 10 rights in giving medication
Right Medication – check at least 3 times
Right dose – correct drug computation
Right time -
Right route-
Right client - Asking patients name and compare it with ID band.
Right client education - education about the medication and why it has been
prescribed, evaluation of the patient’s response, laboratory monitoring of
baseline values and possible side effects.
Right documentation
Right to refuse – nurse first action is to educate the patient on the importance of
medication.
Right assessment
Right evaluation
Discard the first centimeter of ointment when opening the tube for the first time.
Instructing the patient to close eyes for 1-2 minutes and roll the eyeball in all directions
UNIT 2 – PHARMACOKINETICS
¡ PHARMACEUTIC – first phase of drug action for ORAL medications. Oral drugs will
undergo this process before absorption.
¡ PHARMACOKINETICS – how the body moves and process the drugs
¡ Drug Absorption – drug enters the bloodstream from its site of administration.
¡ Factors affecting drug absorption:
¡ Solid preparations are slower to absorb than liquid preparation, it needs to
be dissolved first into a liquid form
¡ Drugs are readily absorbed in acidic than in alkaline environment.
¡ Drug solubility to cross membranes: when the drug is in stomach acid, it
will pass through the stomach walls best if it is an acidic drug.
¡ Lipid soluble drugs are readily absorbed than Non-lipid soluble drugs –
biggest factor determining the concentration of a drug that penetrates the
brain.
¡ Elderly have less gastric acidity that might affect absorption (slower)
¡ Presence of food in the stomach do not always interfere with the
absorption of a drug, some drugs absorbed faster with the presence of
food, other drugs need to ingested in an empty stomach for faster
absorption.
¡ Drug instability in gastric acid - factor associated with drug absorption
that can result in incomplete absorption
¡ Drug Distribution – when drug is in the bloodstream
¡ Drug Metabolism – liver – inactivate drug
¡ First Pass Metabolism – for oral meds – may decrease drug
bioavailability.
¡ First Pass effect - The medication is extensively metabolized in the
patient's liver when it passes through the intestine via the portal vein.
¡ The medication is extensively metabolized in the patient's liver
when it passes through the intestine via the portal vein.
¡ Drug Excretion - kidney
¡ EXCIPIENTS - Allow drug to take on particular size and shape and to enhance drug
dissolution.
¡ DRUG HALF-LIFE is the time it takes for the amount of drug in the body to be reduced by
half. It will help determine the frequency of drugs or dosing.
¡ For example: Ibuprofen 500 mg half - life is 2 hours. So after 2 hours 250 mg will
be excreted out of the body.
¡ Depends on drug metabolism, concentration of drug in plasma and rate of drug
elimination
¡ Half-life determines the dosage interval.
UNIT 3 – PHARMACODYNAMICS
¡ It is the study of the effect of drugs on the body
¡ DRUG AFFINITY - how avidly a drug binds its receptor or how the chemical forces that
cause a substance to bind its receptor.
¡ DRUG EFFICACY - refers to the drug's ability to activate the receptor once it has bound
to it.
¡ MAXIMAL EFFICACY - the point at which increasing a drugs dosage no longer increases
the desired therapeutic response.
¡ MAXIMUM EFFECTIVE CONCENTRATION - The concentration of drug in plasma that above
these, toxic effects are precipitated.
¡ POTENCY – refers to the amount of drug needed to elicit a specific physiologic response
to a drug
¡ Both Drug A and Drug B achieve the same maximum effect, i.e. they have equal efficacy.
¡ However, drug A achieves this effect at a lower dose.
¡ Thus, Drug A has higher potency than Drug B.
¡ Drug A is more POTENT than Drug B
¡ Therapeutic Index - describes the relationship between the therapeutic dose of a drug
(ED50) and the toxic dose of a drug (TD50).
¡ The higher the therapeutic index – the drug is more safe to give.
¡ Drug with lower therapeutic window need to be monitored closely for adverse effects.
¡ TI = TD50/ED50
¡ Example: TD50 is 500 mg and ED50 is 250 mg = 500 / 250 = 2
¡ If a drug Therapeutic index is small, the drug is a narrow therapeutic index drug.
¡ If a drug Therapeutic Index is big, the drug is a wide therapeutic index drug.
Example: The doctor ordered to infused PNSS 1L to run for 16 hours (drop factor 15gtts/cc).
15.625
Clark’s Rule: 𝑐ℎ𝑖𝑙𝑑𝑠 𝑑𝑜𝑠𝑒 = 𝑎𝑑𝑢𝑙𝑡 𝑑𝑜𝑠𝑒 × 𝑤𝑒𝑖𝑔ℎ𝑡 𝑖𝑛 𝑝𝑜𝑢𝑛𝑑𝑠 divided by 150
7 kg = 15.4 pounds
Young’s Rule: 𝑐ℎ𝑖𝑙𝑑 𝑑𝑜𝑠𝑒 = 𝑎𝑑𝑢𝑙𝑡 𝑑𝑜𝑠𝑒 × 𝑎𝑔𝑒 𝑖𝑛 𝑦𝑒𝑎𝑟𝑠 divided by 𝑎𝑔𝑒 𝑖𝑛 𝑦𝑒𝑎𝑟𝑠 + 12
The average adult dose of Amoxicillin is 500 mg every 8 hrs. The child weighs 26 lbs. and is 18
months old.
56 mg = child dose
Fried’s Rule: 𝑐ℎ𝑖𝑙𝑑 𝑑𝑜𝑠𝑒 = 𝑎𝑑𝑢𝑙𝑡 𝑑𝑜𝑠𝑒 × 𝑎𝑔𝑒 𝑖𝑛 𝑚𝑜𝑛𝑡ℎ𝑠 divided by 150
The doctor orders an adult dose of Ibuprofen 600 mg PO PRN. The child’s age is 24 months old.
600 mg x 24 / 150
96 mg