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143 Cards in this Set

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Pharmacokinetics
the study of drug movement through the body. The effect of the body on the drug.
Absorption
the movement of a drug from its administration site into the circulation
Rate of Absorption
how soon the effects of a drug will begin
Amount of Absorption
intensity of the drugs effects
Factors affecting absorption
rate of dissolution, surface area, blood flow, lipid solubility, pH partitioning,
Rate of dissolution
drugs in formulations that have rapid dissolution have a faster onset than drugs with slower rate of dissolution
Surface Area
the larger the surface area the faster the absorption. Small intestine has fastest absorption of oral administered drugs
Blood Flow
the more vascular a site the quicker the absorption. Works on concentration gradient, blood containing newly absorbed drug will be replaced rapidly by drug free blood.
Lipid Solubility
Highly lipid soluble drugs absorb more rapidly.
pH partitioning
drug absorption and elimination ca be affected by acid/base concepts. Also works on concentration gradient. Acid drugs are drawn toward alkaline and vice versa. Important in treatment of overdoses.
Routes of administration
enteral and parenteral and less commonly topical etc.
Enteral Administration
via the gastrointestinal tract
Parenteral Administration
drugs given by penetration of the skin and entry into the underlying tissue
IV
rapid effect maximal degree of control over circulating drug. Usually aqueous. Not reversible.
Drawbacks of IV
Infection, repeat dosage requires patent iv line.
IM
May be used for drugs that are aqueous and non-aqueous. Deltoid and Vastus lateralis quicker than dorso-gluteal or ventro-gluteal admin. Related to blood flow to tissue
Subcutaneous
Dependent on blood flow to the tissue. Slow and constant absorption, non-irritating requires absorption into capillaries.
Oral
most common. Variable in terms of availability. Efficacy may be limited by metabolism. Food in system may affect efficacy/action or delay gastric emptying leading to destruction of drugs.
Distribution
The movement of drugs throughout the body. Dependent upon blood flow to tissues, the availability of the drug to exit the vascular system and to a lesser extent, the ability of the drug to enter the cells.
Speed of Blood flow
Well perfused organs such as brain, heart, kidney and liver receive most of the drug in the first few minutes. Muscle, most viscera, skin and fat are slower to receive drug, from minutes to hours.
Diffusion into Interstitial Compartments
rapid diffusion occurs in most areas because of permeable capillaries. E.g.. Liver capillaries have much of basement membrane exposed by slit junctions which enables rapid diffusion including large plasma proteins.
Blood brain Barrier
no slit junctions in brain so drugs must either pass directly through (lipid soluble) or via active transport.
Biotransformation
Drug metabolism. The most important consequence of metabolism is promotion of renal excretion.
Most important factor in biotransformation
Renal excretion
Factors affecting biotransformation
Induction, first pass effect, extremes of age, nutritional status, competition among drugs.
Induction
Some drugs, acting on the liver, can increase the rate of their own or another drug's metabolism. E.G.. Phenobarbital the classic enzyme inducer
First Pass
rapid inactivation of oral drugs due to liver metabolism.
Metabolism relating to lipophilic drugs
Lipophilic properties that promote a drug's passage through biologic membranes and subsequent access to their sites of action also hinders elimination of the drug.
Usual biotransformation of drugs
usually biotransformed into more polar, inactive metabolites that are easily excreted by body.
Hepatic Metabolism
Metabolites with increased biologic activity or even toxic properties may be created through metabolism E.G.: Tylenol has a hepatotoxic metabolite.
Hepatotoxic definition
chemical-driven liver damage. It is a possible side-effect of certain medications
Excretion
Renal, billiary, fecal, breast milk, lungs, saliva, sweat
Renal Excretion
glomerular filtration, proximal tubule secretion, distal tubular secretion, renal excretion
Plasma Drug Levels
there is a direct relationship between therapeutic and toxic responses and the amount of drug present in plasma
MEC
Minimum effective concentration
MEC definition
the plasma drug level below which therapeutic effects will not occur
Toxic Concentration
the plasma drug level at which toxic effects occur
Therapeutic Window
the range of plama drug levels falling between the MEC and the toxic concentration. Drugs with narrow range of therapeutic window are more apt to cause toxicity. Digoxin is the classic example
Drug Half life
the time required for the amount of drug in the body to decrease(eliminated) by 50%. Drugs with a short half-life but a long dosing interval will lose the MEC
Plateau
when the amount of drug eliminated between doses equals the dose administered. Average drug levels will remain constant and plateau will have been reached.
Techniques for reducing fluctuations in plasma drug levels
Continuous infusion (plasma levels kept constant), constant daily dose reduce size and interval of dosage.
Loading Dose
Large initial dose which achieve plateau rapidly
Maintenance Dose
small doses to maintain plateau
Pharmacodynamics
the study of the biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced. In short, what the drug does to the body.
Dose Response Relationship
Graded relationships. As the dosage increases the response becomes greater
Maximal Efficacy
the largest effect a drug can produce
Potency
the amount of drug that must be given to elicit a response
Drug Receptor
any functional macromolecule in a cell to which a drug binds to produce its effect
Receptor Compatibility
the ability of a drug to bind to it's receptor depends on the size and shape of the drug and it’s receptor, a single receptor can be responsible for regulating several physiologic activities. Drugs mimic or block the actions of the body's own regulatory mechanisms.
Intrinsic Activity
the ability of a drug to activate a receptor following binding and is linked to efficacy.
Agonist
drugs that bind with and activate receptors.
Antagonists
drugs with affinity for receptors but no intrinsic activity
Tachyphylaxis
reduction in responsiveness brought on by repeated doses in short period of time. Rapid tolerance. The MEC is elevated can occur from days to weeks of administration. Metabolic tolerance is caused by the effects of the enzyme induction on drugs. Accelerated metabolism can occur after days or weeks.
Additive Effect
2 drugs with similar properties are taken together.1+1=2 E.G. aspirin and codeine boost analgesic properties if taken together
Synergistic Effect
The response of two drugs taken together is greater than the response of the same drugs taken alone. 1+1=3 E.G. lasix and beta-blockers. Lasix removes fluid and b-blockers block vasoconstriction causing a sharp decrease in bp
Antagonism
One drug inhibits the effect of another. 1+1=0 Vitimin K given to inhibit bleeding from warfarin or Nalazone to antagonize morphine induced respiratory depression
Lipophillic Drug Metabolism
Lipophilic properties that promote a drug's passage through biologic membranes and subsequent access to their sites of action also hinders elimination of the drug.
Penicillin Types
Many Variations Penicillin G: IV or IV only aqueous preparations may be given IV, Penicllin V only Oral.
Penicillin Action
Bactericidal: inhibits synthesis of cell wall, indicated in infections caused by susceptible organizms, treatment for respiratory, genitourinary and gastrointestinal infections
Antibiotic Commonalities
All antibiotics have potential for renal toxicity, diarrhea and hypersensitivity
Bacteriostatic
Inhibits growth but does not kill
Penicillin Contraindications
hypersensitivity, drug interactions, can decrease effectiveness of oral contraceptives
Penicillin: Nursing Implications
Hypersensitivity reactions: risk for injury, Renal impairment: risk for, Knowledge deficit: home care administration
Penicillin Patient Teaching
Do not take any penicillin or derivative (cephalosporin) if allergic, complete full course of drug for greater effectiveness, follow dosing instructions very carefully. Take most PCN on empty stomach, take each dose w/ full glass of water, shake liquids well, report s&s of allergic reactions immediately and do not take w/ fruit juices.
Peak and Trough Values
Determine dose and time drug is to be given based on therapeutic levels
Cultures
Usually taken 30 mins after dose and then 30 mins before next scheduled dose. Help to determine dosage. Temp at which to take cultures varies from facility to facility
Antibiotics-Renal Toxicity
If BUN and creatinine levels are outside of normal range then the kidney ability to excrete wastes may be impaired.
(Lanoxin)Digoxin Classification/Action
Cardiac glycoside. Digitalis is naturally occuring. Increases the force of contractions and decreases hr. Increases CO and blood flow to kidneys and promotes diuresis.
Ionotroph
force of contraction
Chronotroph
heart rate
Lanoxin indications
Heart failure, atrial arrhythmias,
Lanoxin Administration
Oral or IV
Lanoxin Toxicity
rapid loading or digitalization (in order to reach plateau), impaired renal function, age extremes, electrolyte imbalance especially hypokalemia and also hypomagnesemia and hypercalemia
Lanoxin S&S of toxicity
nausea, diarrhea vomiting, visual changes (colored halo), arrhythmias.
Lanoxin related labs
digoxin level, BUN, creatinine, electrolytes.
Digoxin Toxicity
therapeutic range 0.8-2.0 ng/ml.
Digoxin Antagonist
Digibind. Digoxin immune fab.
Digoxin Patient Teaching
Pulse, consult health care provider before taking any other meds, avoid taking missed dose, therapeutic effect is decreased with antacids.
Captopril/Capoten Classification
Antihypertensive/ACE inhibitor
Captopril/Capoten Action
reduces the levels of angiotensin II thereby dilating blood vessels and lowering bp
Captopril/Capoten Indication
For mild to severe hypertension. More effective in young caucasians than in young African Americans (fare better with combo therapy of diruetics and ace inhibitors).
Captopril Side Effects
dry hacking cough (sensitivity in cough center), first dose syncope (bp decreases and fainting after 1st dose or rapid increase in dose), hyperkalemia
Captopril Toxic Effects
Angioedema- swelling of mucosa and submucosa in face, lips, tongue and potentially hands.
Captopril Nursing Implications
Administer 1 hr before meals, monitor bp for first dose syncope, intruct pt to lie down after first dose or after rapid increase in dose, adequate hydration, monitor K levels.
Metoprolol (Lopressor) classification
Beta-Adrenergic blocker. Prevents B-adrenergic receptors from responding to sympathetic nerve impulses. Meta analyst may prevent MI
Metoprolol (Lopressor) Action
Decreses hr, decreases force of contraction, cardiac output, conduction and bp. May cause bronchoconstriction and may decrease glucose metabolism
Metoprolol Indications
Angina, hypertension, arrhythmias, MI
Metoprolol Side Effects
hypoglycemia, severe bradycardia, airway resistance/pulmonary edema, headache, flush dizziness, severe bradycardia, bronchoconstriction, nausea, vomiting diarrhea
CMP
Complete metabolic profile. Blood glucose, BUN, creatinine, lytes.
Metoprolol Nursing Implications
Monitor hr/bp and report significant changes. Instruct pt to report dizziness, fainting, edema, respiratory problems. Take before meals. Diabetic pt can expect insulin changes, Abrupt withdrawal can lead to rebound sympathetic overactivity (rebound htn), monitor labs cbc, cmp.
Furosemide (Lasix) Classification
Loop diuretic
Furosemide (lasix) Action
reduces the body's total water and salt by increasing urinary secretion
Lasix Indications
Fluid volume excess
Lasix Contraindications
electrolyte depletion, allergy (sulfonamide)
Lasix Side Effects
Ototoxicity (ringing), hypokalemia, hypotension, photosensitivity, diarrhea, muscle spasms
Lasix Nursing Implications
Monitor I&O, weight and vitals. Teach pt to report s&s of ototoxicity. Monitor cmp. Sunscreen.
Nitroglycerine Classification
Organic Nitrate, Oral (Iserdil), IV, sublingual, transdermal
Nitroglycerine action
Acts directly on smooth muscle to promote venous dilation, decreases venous return, decreases oxygen demand by decreasing workload
NTG side effects
headache, hypotension, tachycardia (rare), tolerance
NTG Nursing Implications
Observe for relief of acute chest pain, teaching regarding diet, weight, lifestyle factors related to angina, teaching regarding compliance with drug therapy
Heparin Classification
anticoagulant. IV or sub q. First Pass drug. One and 1/2 to 2 times control is usualy considered therapeutic
Heparin Action
disrupts production of fibrin thereby disrupting the coagulation cascade. Inhibits formation of clots but does not bust old ones up. Immediate after IV and w/in 20 minutes of sub-q
Heparin Indications
prevention of DVT, and pulmonary embolism in susceptible pt. Prevention of clotting during cardiac surgery, dialysis.
Heparin Lab
PTT
Heparin Antagonist
protamine sulfate
Heparin Contraindications
bleeding, high risk for bleeding, vitamin k deficiency, severe hypertension, advanced kidney or liver disease.
Warfarin Classification
anticoagulant.
Warfarin Action
acts in liver to prevent synthesis of vitamin K dependent factors. Onset is 3-5 days after administration
Warfarin Antagonist
Aqua-Mephyton (vitamin K)
Warfarin Indications
long term prevention of thromboembolic disorders
Warfarin Contraindications
bleeding, high risk for bleeding, vitamin k deficiency, severe hypertension, advanced kidney or liver disease.
Warfarin Labs
PT and INR (weekly for the first month) dose adjustment highly individual, Range of 2:3 is acceptable
Enoxaparin (Lovenox)
Low molecular weight heparin sq admin.
Lovenox Antagonist
protamine sulfate
Lovenox Lab
Does not require lab monitoring
Anticoagulants Nursing Implications
Monitor I&O, monitor labs, monitor for bleeding, instruct pt to report bleeding
Phenytoin (dilantin) Classification
Anticonvulsant or antiepileptic drug
Dilantin Action
Stabilization of neuronal membranes thereby limiting spread of seizure activity.
Dilantin Indication
Prophylaxis and Rx of grand mal seizures
Dilantin Administration
Oral or IV (can cause hypotension IV), Long half life. Not compatible with anything in IV line only saline. Mixing causes chalky precipitate.
Dilantin Contraindications
Heart block, dilantin slows blood flow/ hr. May increase blood glucose caution in diabetics, concurrent use of antacids may decrease efficacy.
Dilantin Nursing Implications
Adverse effects (GI, CNS) most likely to occur in geriatric population
Dilantin Labs
Dilantin level, hepatic profile (highly metabolized in liver), cbc. Flush IV before admin.
Dilantin Patient Teaching
proper dose, compliance with therapy, if dose is missed do not double up, avoid abrupt discontinuation, avoid alcohol. Take immediately after meals.
Sodium Bicarbonate Special Note
Not compatible with other drugs IV
Zofran (Ondansetron) Classification
Antiemetic
Zofran Action
blocks central serotonin receptors thus blocking the vomiting center.
Zofran Indications
Emetogenic cancer therapy as well as other causes of NV (used pre-op and/or post-op)
Zofran Nursing Indications
Management of possible headache, management of constipation, report cv symptoms
Zofran Side Effects
constipation, headache common, cardiovascular changes
Insulin Classifications
Parenteral antidiabetic agent/ hormone
Insulin Action
promotes the uptake of glucose by cells as well as other functions related to carbohydrate metabolism
Insulin Types (examples)
regular (rapid onset short duration), Lispro (humalog) rapid shorter acting analog of regular, Neutral Protamine Hagedorn (NPH) intermediate acting, Ultralente: long acting, Glargine (Lantus) long acting
Insulin
100 units per ml. Regular only insulin given IV. Rotate sites, monitor blood glucose levels.
Insulin Nursing Implications
Most serious consequence of insulin therapy is overdose manifested by: profuse diaphoresis, confusion, irritability, incoherent speech, hunger, headache, palpitations, tachycardia, blurred vision, convulsions and coma
Insulin Patient Teaching
administration, diet, carry quick form of carbohydrate, Sx hypoglycemia, identification
Albuterol (Ventolin)
Beta 2 Agonist, stimulates the Beta 2 receptors to relax smooth muscle in bronchioles.
Albuterol Adverse
tremors, tachycardia
Prednisone Classification
Glucocorticoid
Prednisone Action
Increases synthesis of glucose, suppresses immune response
Prednisone Indications
RA, asthma
Prednisone Adverse affects
Poor wound healing, hyperglycemia, electrolyte imbalances.
Prednisone Nursing Implications
monitor for hyperglycemia