| Question |
Answer |
| A drug that effects conduction velocity (CV) is referred to as | Dromotropic |
| A drug that effects Heart rate (HR) is referred to as | Chronotropic |
| A drug that effects Force of contraction (FOC) is referred to as | Inotropic |
| Atoms that are the same but have right and left hand arrangements are called | Stereoisomers |
| The analysis of the drug itself to evaluate its potency | Assay |
| If a patient experiences a completely unique response that is specific to that person, it is called | Idiosyncrasy |
| Blocking a receptor site from being stimulated from other chemical mediators and inhibit the normal response, is called | Antagonist |
| Name the study of the metabolisim and the action of medications within the body, with particular emphysis on the time required for absorption, duration of action, distribution in the body, and excretion. | Pharmacokinetics |
| What nerves carry messages from the brain to the muscles and all other oragons of the body | efferent nerves |
| A patient developes a tolerance to a medication, because of a prolonged administration of a seperate medication | Cross-tolorance |
| What kind of effect occurs after the drug is absorbed by any route and distributed by the blood stream. | Systemic effects |
| The way in which a medication produces the response we intended | Pharmacodynamics |
| What kind of effects result from the direct application of a drug to a tissue | Local effects |
| A medication that stimulates a response in a receptor site is called | Agonist |
| What nerves carry sensory impulses from all parts of the body to the brain | Afferent nerves |
| What class hass the lowest abuse potential, although they may lead to limited dependence | schedule V |
| What class has a low abuse potential and limited dependence potential | Schedual IV |
| The attraction between a medication and it's receptors is referred to as | Affinity |
| A procedure for determining the concentration, purity, and/or biological activity of a substance by measureing it's effect on an organism, tissue, cell, or enzyme | bioassay |
| The drugs that can be administered through the ET tube or navel. Name all 5 | Naloxone, Atropine, vasopressin, epinephrine, lidocaine |
| Drugs that may lead to low or moderate physical dependence or high psychologic dependence fall under what calss | Schedule III |
| For a drug to carry the USP label the amount of active ingredients must be within | + - 5% |
| Name the route of administration that is between the cheeks and Gums | Buccal route |
| What drugs have a very high abuse potential and may lead to a sevfere addiction, but have a lower propensity for addiction then schedule I | Schedule II |
| WHat schedule drugs have the highest abuse potential and a propensity for severe dependence. None of them are accepted in medical practice. | Schedule I |
| What was the name of the first federal legislation in the us aimed at protecting the public, and when did it come? | The pure food act in 1906 |
| The study of medications and their effects or actions on the body | Pharmacology |
| Name the medications 6R's | Right Patient, dose, route, time, medication, PCR documentaion. |
HHS Shrek
