principles pf drug classification I Flashcards
nurses should always with meds
understand before administration
know usual dose
know route
side effects and adverse reactions
major med interactions
and apply nursing process at all times
side effect vs adverse effect
SE: expected
AR: unexpected
nursing process example
pain
assess: pain, RR, HR
plan: for meds
Diagnosis: pain
implement: pain meds
evaluate: pain scale
rights to meds
right:
drug
dose
time
route
patient
caveat to the rights to meds
use clinical reasoning to determine if the med should or not be administered
generic name verse trade name
generic: all lower case
acetaminophen
trade: upper case first letter
Tylenol
Advil
HCPs should always use the generic name when writing prescriptions
precription or legend drug
requires a prescription in order to get
non-prescription or over the counter (OTC) drug
dont need prescription
usually at lower dose than prescription drugs
(200 tylenol vs 800mg prescription tylenol)
see doctor if med dose does not work. do not take more than instructed
4 main sources of drugs
plants (digitalis, colchicine)
animals/humans (insulin from pigs) (epi)
minerals/mineral products (iron, iodine, zinc)
synthetic/ chemical substances (made in lab)
what is similar per class
-class name
-mechanism of action
-SE/AR
-contraindications
-precautions
-significant med interactions
-specific nursing action to be taken before, during, and after administration
resources for drug info
us pharmacopia: highlightd info to reduce drug risks
PDR physicians desk reference: drug inserts/pics does snot contain nursing info
nursing drug books: condensed PDR toward nursing
Apps: get updated
on going education
-should always continue to learn for .edu or .org
-empolyer must give updated med info
-nurse is responsible for being up to date
-ignorance to new info will not help in court
-use multiple sources
what are nurses responisble for with their education
staying current in all areas of practice
liable for their actions and omissions of their duties and duties delegated to others
history of meds
prior to 1906 meds were not regulated
1906 the pure food and drug act
passed to protect from mislabeled drugs
designated us pharmacopeia and the national formulary as official standards of publications
1914 harrison narcotic act
first federal law aimed at curbing drug addiction
established the word narcotics
1938 federal food, drug, and cosmetic act
Prevented new drugs from being marketed before being tested for safety
1952 durham-humphrey amendment
Specified how legend, or prescription, drugs and refills could be ordered and dispensed
Also recognized OTC meds
1962 kefauver-harris amendment
Required proof of both safety and efficacy of a new drug before it could be approved
1971 controlled substance act
Increase research, prvent abuse, provide rehabilitation
Improved handling of controlled substances
Classifies meds according to their potential for addiction
1973 The drug enforcement administration (DEA)
dea became sole legal drug enforement agency in the us
federal offense to give someone your prescription
1983 Orphan Drug Act
authorized the FDA to provide grant money to encourage research for rare chronic diseases