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chapter 1
intro to pharmacology
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any substance that is taken to prevent, cure, or reduce symptoms of a medical condition
drug
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when someone is dehydrated, water (saline) solution may be infused into patient to treat a condition
water (saline) is considered a drug
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when someone with a vit c deficiency may be administered to cure scurvy
vit C is considered a drug
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study of medicine
Pharmacology
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application of drugs for prevention of disease and treatment of suffering
pharmacotherapy
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expansive subject from understanding how drugs are administered, where they traveled in the body and the actual response they produce
pharmacology
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begins when the patient experience signs and symptoms that cause dissatisfaction in health status
pharmacotherapy
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nurse's role in pharmacology
- -administer drugs to pt.
- -monitor and document the effects of drug administered
- -design interventions that meet pt. health goals
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drugs may elicit different responses depending on pt. factors:
age, gender, race, body mass, health status and genetics
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goal of pharmacotherapy
select the perfect or ideal drug for the pt
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classification of drug
- -therapeutic
- -pharmacologic
- -mixed categories
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-drugs that offer treatment of disease
-what is being treated by the drug
-uses prefixe anti-
therapeutic classification
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Pneumonia - use of antibiotic
therapeutic
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-describe how the drug acts
-drug mechanism of action
-uses drug's chemical name
Pharmacologic
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underactive thyroid gland - supplement with synthetic thyroid
pharmacologic
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drugs that overlap into different or both therapeutic and/or pharmacologic classifications
mixed categories
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HTN meds beta blockers
-lowers bp (P)
-therapeutically use to treat migrain (T)
mixed categories
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compare all drugs in a classification to one particular drug
-ex: others kinds of hormone secretion meds are developed and compared to Prozac which makes it the prototype
drug prototype
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-related to chemical and molecular structure
-uses standard nomenclature
ex. Acetylsalicylic Acid
chemical name
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-derived from chemical name
-less complicated and easy to remember
-only one generic name for each drug
ex: Aspirin
generic name
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-proprietary name given by manufacturer
-"brand name"
ex. Ecotrin (aspirin)
trade name
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competing companies are not allowed to market generic versions of product
exclusivity
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drug with more thatn one active generic ingredient
combination drugs
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-rate of extent to which active ingredient is absorbed from a drug product and becomes available at site of drug action to produce its effect
-measure how long a drug takes to exert its effect
-compre brand name drugs and their generic equivalents
Bioavailability
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nurse's responsibilities:
- -nurses should know what drug is ordered (name and drug classification)
- -indications and contraindications
- -adverse rxn or side effects
- -administration (does and route)
- -nursing considerations (growth and dev'tmental factors
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chapter 2
drug regulations
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-inform the public and protect them from unsafe and ineffective products
-protect the public so they can receive safe meds
drug legislations
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-ability to legally make or sell a drug
-contained a clearly indentified brand name
-often harmless (ineffective) containing coloring, flavoring or aromatic subs
-cocaine heroin and morphine were distributed to these meds
Patent Medications
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-keep records of dispensed narcotic drugs
-ILLEGAL to possess narcotics WITHOUT prescription
-precribe narcotics only for treatment. not to addicts
1914 - Harrison Narcotic Act
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prevent the sale of drugs that has not been thoroughly tested for safety before marketing
1938 - the Food Drug and Cosmetic Act
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difference between safer drugs, which may be sold OTC or require prescriptions
1951 - Durham Humphrey Amendments
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-development of drugs to treat rare or unusual disorders
-legislation and drug manufacturers offered dev't grants and expenses to approved orphan drugs
1983 - Orphan Drug Act
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clear labelling of dietary supplements and remove supplements that cause a significant public risk
1994 - the Dietary Supplement Health and Education Act
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provide seniors and those with disabilities a prescription drug benefit under medicare
2003 - Medicare Prescription Drug Improvement and Modernization Act
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Drug Standards:
- -US Pharmacopeia - National Formulary
- -FDA
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medical reference summarizing standards of drug purity, strength and directions for synthesis
Pharmacopeia
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every pill in a bottle has the same ingredient as th other pill
USP-NA
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-protect the public health by assuring efficacy, safety and security
-speed innovations that make medicines and foods more effective, safer and affordable
-get accurate science-based info
usFDA
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drug approval process
all drugs must be approved by the FDA before they can be sold in the US
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1st stage, extensive lab testing
-perform testingon human and animals to examine drug effectiveness
-goal is to determine drug action and predict whether drug will cause harm to human
-FDA does not regulate this testing
Preclinical Research
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pharmaceutical company sumbits an application to FDA that contains animal and cell testing data
Investigational New Drug
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2nd stage, longest part of drug approval
includes 3 different stages
clinical phase trials
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focuses on safety/ 20-80 health volunteers
Phase 1
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-focuses on effectiveness and safety, several hundred pt.
-effectiveness compared to Placebo
Phase 2
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drug-drug interactions
large # of pt with diseases are given the drug to determines pt variability
Phase 3
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signals pharmaceutical company that the drug is ready to sell
NDA - new drug application
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stage 4 of drug approval process
survey for harmful drug effects in larger population
Postmarketing Surveillance
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predominantly used in drug research
Caucasian males
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excluded due to hoemonal changes and pregnancy
women
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in order to obtain a prescrption drug:
health care provider must provide a written authorization with proper amount and frequency
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do not require an order from a health care provider. may treat themselves if instructions are followed properly
OTC
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why pt. prefer OTC than Prescription drugs?
Otc drugs may be obtained easily w/o making an appt, saves time and money
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former RX drugs that are now OTC
Zyrtec, Claritin, pepcid, Prilosec
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drugs that have significant potential for abuse, 5 categories of schedules
-regulated according to their potential for abuse
-locked in cabinet
Scheduled drugs
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highest addictive, not accepted for medical use/treatment in US, not allowed to prescribe
ex: Heorin, LSD, Peyote
Schedule I
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-highest addictive, drug has accepted to be used for treatments in US with severe restrictions
-ex: must use special order form, written and sign by provider to obtain the drug; telephone orders are not permitted
Ex: opioids (morphine), demerol, dilaudid
schedule II
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less potential for addiction, currently accepted in medical use treatment in US
-ex: codaine, hydrocodone, immediate-acting barbituates
schedule III
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lower potential for addiction, accepted medical use for treatment in US
Ex: Benzodiazipines, long-acting barbituates
schedule IV
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lowest potential for addiction, currently accepted medical use in US
Ex: cough medicines with codaine, lomotil
schedule V
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