test 1 Flashcards
(40 cards)
Chemical name
– chemical structure of drug
Generic name
– nonproprietary name
Trade/Brand name
– name owned and marketed by a pharmaceutical company
Contraindications
Contains warnings as to particular patients or situations in which the drug should not be used
Drug Interactions
- Modification of the effect of a drug when given with another drug
- Results in either a decrease or increase in the action of the drug
- Beneficial (Drug combination therapy)
- Harmful (Adverse side effects)
Three Types of Drug Interactions
- Additive interactions
- Synergistic interactions
- Potentiation interactions
Additive Drug Interactions
-sum of the effects of two drugs given together is equal to each of them given separately but at the same time
Synergistic Drug Interactions
-summation of each individual drug’s activity exceeds the sum of the two individual drugs
Potentiation Drug Interactions
-One drug (which has no direct effect) increases the response of the other drug, which normally has a lesser effect
Adverse Drug Reactions (ADR)
•Unintended side effects from a drug
•At least 5% of hospitalizations are the result of an adverse drug reaction
– tremors, bronchospasms, headaches, vomiting, photosensitivity etc.
•Not all ADRs are allergies
Drug Allergy
- Drug allergies are immune-mediated and induce a hypersensitivity reaction (Mild-hives, Severe-anaphylactic shock)
- Drug allergies are only one example of an ADR
Pharmacokinetics
- what the body does to a drug
- Absorption, distribution, metabolism, and elimination
Pharmacodynamics
-what the drug does to
the body
Absorption
How a drug moves from its site(s) of administration into plasma
absorption of the drug is based on
- size of the drug (smaller the easier)
- ionization of the drug (non-ionized pass through membrane easier)
- lipid solubility (lipophilic easier to pass through than hydrophilic)
Distribution (pharmacokinetics)
-The dissemination of a drug throughout the body, such as plasma, tissues, or organs
•Bloodstream is the major vehicle for distribution
Distribution Influenced by
- Blood flow
- Fat or water solubility
- Protein binding
Metabolism (pharmacokinetics)
-The biotransformation of a drug into other secondary components called metabolites
•Preparing drug for elimination
•Drug becomes more water soluble to enhance elimination
Elimination (pharmacokinetics)
- The processes that remove a drug from the body in urine, bile, or feces
- Drugs can also be excreted via the pulmonary system, skin, hair, saliva, and expired air
routes of administration determined by
- Determined by property of drug (Water or lipid soluble, Ionization)
- Desirability of a rapid onset
- Need for long-term treatment
- Restriction of delivery to a local site
Enteral (through digestive tract) Administration
- Administering drug by mouth (Swallowed, Under tongue (sublingual), Between gums and cheek (buccal))
- Most common
- Most convenient
- Most economical
- Safest
Oral Administration
•Easily self administered •Toxicities/overdoses may be overcome with antidotes •Low gastric pH inactivates some drugs •MOST COMPLICATED DRUG ABSORPTION ROUTE
Oral Preparations: Enteric coated
- Chemical coating that protects drug from stomach acid
- Drug dissolves in the intestine (less acidic)
- Useful for drugs that are acid unstable
Extended-Release Preparations
- Drugs contain special coatings or ingredients that control drug release
- Allows slow absorption
- Prolonged duration of action
- Can be dosed less frequently
- Improves patient compliance
- Useful for drugs with short half-lives