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Pharmacology
The science of the study of drugs including their compositions uses and effects
Drugs
Any chemical substance that has an effect on the physiological processes of an organism
Clinical Pharmacology
The science that focuses on the effects of drugs in the human body which includes both patients and well individuals
Therapeutics
A branch of medicine that deals specifically in the treatment of diseases
Oral
swallowed by mouth as a pill liquid tablet capsule or lozenge
Rectal
suppository inserted into the rectum
Intravenous
injection into vein with syringe or into intravenous (IV) line
Infusion
injected into vein with an IV line and slowly dripped in over time
Intramuscular
Injected into muscles through skin with a syringe
Subcutaneous
Injected into the subcutaneous area under the skin
Intradermal
Injected into the dermal layer of the skin just below the epidermis
Topical
Applied to skin (superficial level) such as lotions, moisturizers, creams, and ointments
Enteric
Delivery directly into the stomach with a G-tube or J-tube
Parenteral
All kinds of injection
Nasal
Sprays or pumps that deliver drug into the nose
Inhaled
Inhaled through a tube or mask (e.g. lung medications)
Otic
drops into the ear
Ophthalmic
Drops gel or ointment for the eyes
Sublingual
Dissolved under the tongue
Buccal
Held inside the cheek
Transdermal
A patch on the epidermal layer where the medication is being absorbed by the skin
Dosage
Refers to the amount of medication administered
Route
Refers to the route of medication administration
Timing
Refers to the frequency, intervals or timing of drug administration
Pharmaceutic Phase
The first phase for orally-administered drugs
Necessary for it to take effect
Oral medications are needed to be converted to a soluble liquid form to pass the semipermeable layer
Disintegration
Manual breakdown of tablets into smaller pieces
Dissolution
The process of dissolving smaller particles in the GIT before absorption
Excipients
Fillers and inert substances that take a particular size and shape which enhances the dissolution phase
Enteric Coated Medication
Medications that are intended to be dissolved in the small intestine (an area that is less acidic compared to the stomach)
Pharmacokinetic Phase
The second phase which determines what the body does to the drug
Determines how much of the administered dose gets to its site of action
Absorption
Movement of drug from the site of administration to the bloodstream
Passive Absorption
Drug movement across the membrane that does not require energy (e.g. diffusion)
Active Absorption
Drug movement that requires effort or a carrier (e.g. enzymes and different protein carriers) to move the drug against a concentration gradient
Bioavailability
A subcategory of absorption described as the percentage of the administered drug dose that reaches the systemic circulation (the proportion of the drug that reaches its site of action)
Distribution
The transport of a drug in the body by the bloodstream to its site of action for it to take effect
Process where drug becomes available to body fluids and body tissue
Metabolism
Process which involves the biologic transformation of a drug into an inactive metabolite in order for it to not be toxic (body inactivates or biotransforms drugs)
Half-Life
The time it takes for half of the drug concentration to be eliminated
This will determine the frequency of drug administration for you will be able to determine or compute the time it takes to reach a steady state serum concentration of the drug
Prodrugs
Compounds that are pharmacologically inactive when administered (no therapeutic effect), however, it undergoes conversion to its active form (increased therapeutic effect) via metabolism
Excretion
Process of removal of drug components in the body
Pharmacodynamic Phase
Science dealing with interactions between the chemical components of living systems and the foreign chemicals, including drugs that enter those systems
Study of biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced
Onset of Action
Time it takes to achieve the minimum effective concentration
Peak of Action
Time it takes for the drug concentration to reach its highest blood or plasma concentration
Minimum Toxic (Maximum Therapeutic Concentration)
Highest possible serum level of a medication that yields a therapeutic effect
Duration of Action
Length of time of the pharmacologic response
Therapeutic Range
Range of drug levels in the blood of a patient in which the drug has desired effects upon the body
Area between minimum effective concentration and maximum therapeutic/minimum toxic concentration
Therapeutic Index
A quantitative measurement on the relative safety of the drug being administered
Dose Response
Relationship between the minimal versus the maximal amount of drug dose needed to produce the desired drug response
Loading Dose
A large or significantly higher initial dose of the drug given to achieve a rapid minimum effective concentration (onset of action) in the serum concentration
Maximal Efficiency
Maximum response achievable from an applied or dosed agent
Primary/Desired Effect
When the therapeutic goal of the medication is achieved (the drug does what it is supposed to do)
Side/Secondary Effect
Any effect caused by the drug other than the intended therapeutic (primary) effect, which can either be beneficial or not
Adverse Effects
Pertains to more severe symptoms or problems that arise related to medication administration
Idiosyncratic Responses
Unexpected responses
Hypersensitivity/Allergic Reactions
An antibody-antigen reaction brought about by drug administration
Several reactions may manifest such as hives, rashes, pruritus or skin
Anaphylactic Shock
Unresolved allergic responses that are usually life threatening and may usually result to cardiac arrest or respiratory collapse
Addictive Effect
Two drugs with similar action are taken for a double effect
Synergistic Effect
Combined effect of the two drugs is greater than the sum effect if given alone
Antagonistic Effect
One drug contradicts/interferes with the effect of the other
Displacement
Displacement of one drug from the protein binding sites
A highly-protein bound drug, in the presence of a drug with a higher percentage of protein binding effects, is bumped off from the protein it is initially bound to
Interference
The first drug inhibits the metabolism of the other drug
Vital for penicillin-derivative antibiotics
Incompatibility
Deterioration on the drug potency if both drugs are given at the same time (both drugs will destroy each other)
Toxicology
The study of poisonous effects of drugs and the symptoms, mechanism, treatment, and detection of poisoning
Pharmacognosy
The study of physical and chemical properties of substance from natural sources or synthetic sources in order to develop drugs.