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Pharmacology
the study of chemicals-drugs-on living
tissues and how those chemicals help diagnose, treat,
cure, and prevent disease or correct the pathophysiology
of living tissues.
pharmakon
greek word for drugs
logos
greek word for science
what are the sources of drugs
plants, minerals, animals
animals
they contain hormones that can be reclaimed and given to patients who need increased hormonal levels to maintain homeostasis
PLANTS
have medicinal qualities and have been used for
centuries as natural remedies for injuries and illnesses.
minerals
are inorganic crystal substances that are found naturally on earth.
give the 3 names of drug
chemical name, generic name, brand name
chemical name
identifies chemical elements and compounds that
are found in the drug.
generic name
it is the universally accepted name and considered the
official proprietary name for the drug.
generic name
name appears on all drug labels and is the official name listed in official sources such as the Physicians Desk Reference (PDR)
brand/trade name
This restricts the use of this name to that particular company.
Many brand names may exist for the same chemical compound.
Digitalis
Drug obtained from the leaves of the foxglove plant; used to treat congestive heart failure and cardiac arrhythmias and to strengthen heart contractions.
premarin
Drug containing estrogen recovered from mare urine; used as hormonal therapy for menopausal symptoms.
Insulin as an Animal/Human Source Drug
is a hormonal drug used to regulate blood sugar in patients with diabetes mellitus and can be recovered from humans using DNA technology.
iron
Mineral used in supplements for iron deficiency; iron is part of hemoglobin, which carries oxygen throughout the body.
Synthetic/Chemical Derivatives
Man-made drugs produced through chemical synthesis by rearranging chemical derivatives to create a new compound.
sulfonamides
Synthetic drugs used to treat infections such as bronchitis, pneumonia, and meningitis by preventing bacterial growth.
herbals
Non-woody plants with medicinal qualities; some are classified as dietary supplements rather than drugs.
herbal regulation
Unlike drugs regulated by the FDA, dietary supplements are not tested and regulated in the same way; purity and strength may vary.
herbal manufacturing
Lack of control over manufacturing can result in inconsistent strength and possible contamination.
herbal claims
Distributors cannot claim that an herbal product cures a disease; they may only describe its effect on the body.
herbal side effects
Herbals can cause unwanted side effects and may interact with prescription drugs.
herbal medication history
Healthcare providers should encourage patients to report all herbal preparations they use.
Prescription/Legend Drug
Drug that can only be obtained with a prescription from a licensed practitioner.
Durham-Humphrey Amendment
1952 amendment requiring certain drugs to be accessible only by prescription.
Drugs Commonly Requiring Prescription
Injectable drugs, hypnotics, narcotics, habit-forming drugs, drugs unsafe without professional supervision, and certain new drugs still being investigated.
hypnotic drug
Drugs that depress the nervous system.
nacrotics
Drugs that relieve pain, dull the senses, and induce sleep.
habit forming drugs
Drugs that can lead to dependence or habit formation.
OTC drugs
drugs available without prescription
Therapeutic Effect
Intended physiological effect or reason a drug is given.
Antibiotic Therapeutic Effect
Destruction of bacteria is an example of a therapeutic effect.
side effects
Physiological effect that is not the intended action of the drug.
Antihistamine Side Effect
Drowsiness is an example of a side effect.
adverse effect
Unwanted effect that can be harmful to the patient.
drug safety
Drugs undergo rigorous testing before being approved for human use.
acute toxicity
Dose that is lethal to 50% of laboratory animals tested.
Subchronic Toxicity Study
Usually involves daily drug administration for up to 90 days in at least two animal species
Chronic Toxicity Study
Usually lasts for the lifetime of the animal, depending on the intended duration of drug use in humans.
therapeutic index
Ratio between the median lethal dose and the median effective dose.
digoxin
Example of a drug with a narrow margin of safety that requires frequent plasma-level monitoring.
vitro studies
Laboratory test-tube studies used to determine drug metabolism and other effects in humans.
Phase I: Initial Pharmacological Evaluation
Drug is given to a small number of healthy volunteers to determine safe dosage levels, toxicity, tolerated dose, and pharmacokinetics.
Phase II: Limited Controlled Evaluation
Drug is tested in people with the targeted disease to evaluate effectiveness, side effects, and optimal dose-response range.
Phase III: Extended Clinical Evaluation
Involves many physicians and large groups of participants to gather enough information to justify continued use.
Phase IV: Post-Marketing Follow-Up
Studies conducted after FDA approval to continue monitoring the drug.
Category A
Adequate and well-controlled studies show no risk to the fetus during the first trimester or later.
category b
Animal reproduction studies show no fetal risk, but adequate controlled studies in pregnant women are unavailable.
category c
Animal reproduction studies have reported adverse effects on the fetus, however there are no well-controlled studies in humans but potential benefits may indi cate use of the drug in pregnant women despite potential risks
category d
Positive human fetal risk has been reported from investigational or
marketing experience, or human studies. Considering potential benefit
versus risk may, in selected cases, warrant the use of these drugs in
pregnant women.
category x
Fetal abnormalities reported and positive evidence of fetal risk in humans is available from animal and/or human studies. The risks involved clearly outweigh the potential benefits. These drugs should not be used in pregnant women
drug order
Instruction from a healthcare provider to give medication to a patient.