module 1 Flashcards
- the study of drug action.
- It involves looking at the interaction of chemical substances with the systems in our bodies, as well as identifying ways in which our
biological systems affect drugs. - the INTERACTION of drugs and
living organisms.
PHARMACOLOGY
means Drugs /medicine
PHARMAKON
means to study
LOGOS (LOGY)
a chemical substance, [other than food and water] derived from either natural, synthetic, microbial, and other source, presented in different dosage forms used in prevention, diagnosis, relief or alleviate, as supplement [to enhance physical or mental well-being] and treatment or cure of diseases.
DRUG (MEDICINE)
drug treatment of parasitic or neoplastic disease in which the drug has a selective effect on the invading cells or organisms.
CHEMOTHERAPY
every drug is given a __ which is a precise description of its chemical constituents and indicates the arrangement and position of atoms or atomic groups.
- These are long and too cumbersome to remember.
CHEMICAL NAME
drugs are also known by generic, non- proprietary. This is the name given to a drug after it might have been found to be of therapeutic use. It is the name with which the drug is described in official books of reference like pharmacopeias.
GENERIC NAME
It is also the name that is authoritatively accepted by a scientific body.
- easier to read and pronounce than the drug’s chemical name.
GENERIC NAME
- (also known as proprietary or trade name) is the name given to a drug by its manufacturer. A drug may have several brand names, depending on the number of manufacturers.
- Unlike chemical and generic names,
these are easy to remember, short, catchy and most often suggestive of the drug component.
BRAND NAME
name listed in official books or Pharmacopoeia
- It is the same as the generic name.
OFFICIAL NAME
The books containing the standards of drugs and related substances are known as
PHARMACOPOEIAS
collectively these books are known as
DRUG COMPENDIA
The word pharmacopoeia is derived from two Greek words: __
PHARMAKON AND POIEO
USP and NF meaning
UNITED STATES PHARMACOPOEIA
NATIONAL FORMULARY
drug classification: grouping
according to chemical structure.
CHEMICAL CLASSIFICATION
drug classification: grouping according to therapeutic indication.
THERAPEUTIC CLASSIFICATION
Drug that relieves pain.
ANALGESIC
A drug that causes loss of sensation.
ANESTHETIC
drug used in controlling or preventing allergic symptoms.
ANTI ALLERGY
drug that helps
prevent the symptoms of asthma.
ANTI-ASTHMA
drugs that reduce or block histamines, so they stop allergy symptoms.
ANTIHISTAMINES
a medicine (such as penicillin or its derivatives) that inhibits the growth of or destroys microorganisms.
ANTIBIOTIC
a drug used to prevent or reduce or lower an elevated body temperature or fever.
ANTIPYRETIC
are medicines that suppress coughing, also known as cough suppressants.
ANTITUSSIVE
drug to dissolve mucus or phlegm.
MUCOLYTIC
a drug that helps loosen mucus so you can cough it up.
- It does this by increasing the water content of the mucus, thinning it out, and making your cough more productive.
EXPECTORANT
drug classification: grouping according to mechanism of action.
PHARMACOLOGIC CLASSIFICATION
drugs not approved for medical use. High potential for abuse.
Examples: hallucinogens, heroin, marijuana
CI OR CSI
drugs having medicinal use. High potential for abuse.
Examples: Barbiturates, CNS Stimulants, Hypnotics, Narcotic Analgesics, Sedatives
CII OR CSII
drugs less potential for abuse than CII; Potential for dependence.
Examples: Male sex hormones, Other CNS Stimulants
CIII OR CSIII
drugs less potential for abuse than CIII; Limited potential for Dependence.
CIV OR CSIV
drugs containing small amount of controlled substances; limited
potential for abuse.
Examples: Antitussives like DM; Antidiarrheal like loperamide.
CV OR CSV
FDA pregnancy category: controlled studies show no risk: adequate, well-controlled studies in pregnant women have failed to demonstrate risk to the fetus
CATEGORY A
FDA pregnancy category: no evidence of risk in humans: either animal findings show risk, but human findings do not; or, if no adequate human studies have been done, animal findings are negative
CATEGORY B
FDA pregnancy category: risk cannot be ruled out: human studies are lacking, and animal studies are either positive for fetal risk or lacking as well. however, potential benefits may justify potential risk
CATEGORY C
FDA pregnancy category: positive evidence of risk: Investigational or postmarketing data show risk to the fetus. Nevertheless, potential benefits may outweigh risks.
CATEGORY D
FDA Pregnancy category: Contraindicated in pregnancy: Studies in animals or humans, or investigational or postmarketing reports, have shown fetal risk that clearly outweighs any possible benefit to the patient.
CATEGORY X
Pure drugs must contain only one chemical agent; but this is rarely attainable, because there shall always be additives or called excipients.
PURITY
is the drug’s strength which depends on the concentration of active drug or ingredient.
POTENCY
the measure of the rate and extent of drug transfer from site of administration to systemic circulation.
BIOAVAILABILITY
Drugs safety is measured by the incidence and severity of adverse reactions.
Note: Complete safety of drug cannot be determined regardless of testing before release of a drug.
SAFETY