• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/200

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

200 Cards in this Set

  • Front
  • Back
Requires close monitoring because of a narrow therapeutic range
Coumadin
Requires frequent dose adjustments because of individual dose response
Coumadin
High potential for interactions involving food and drugs
Coumadin
Requirements can lead to ineffective therapy or toxicity
Coumadin
Slow onset, full effect is not seen for a week
Coumadin
Usually given in the evening following careful attention to lab results
Coumadin
PR (1.5 to 2.5 x control)
INR (2.0 to 3.0 OR 3.0 to 4.5)
Coumadin
Therapy duration can range from several months to lifelong
Coumadin
Increased effects seen with chondroitin and garlic
Coumadin
There is an increased bleeding risk seen with cayenne, feverfew garlic, ginger, and Gingko biloba
Coumadin
Decreased effectiveness of the medication is seen with the use of green tea, ginseng, and goldenseal
Coumadin
Foods high in vitamin K should be avoided or used sparingly during therapy
Coumadin
The use of alcohol should be restricted if not avoided to maintain effective drug therapy
Coumadin
Referral to a dietitian is always indicated
Coumadin
Bleeding is the major adverse effect and is usually seen at higher dosage levels
Coumadin
Monitor for GI side effects
Coumadin
If client experiences adverse effects or toxicity, withhold dose
Coumadin
Antidote is phytonadione (Vitamin K)
Coumadin
Can be administered IV or sub cut
Heparin
Activated partial thromboplastin time (APTT)
Heparin
Infusion pump
Heparin, Meds for hypertensive emergencies
It should be infused through a dedicated IV line b/c of its incompatibility profile
Heparin
Antidote: protamine sulfate
Heparin
do not give antidote more than 50 mg in 10 minutes
Heparin
Significant drug interactions: ASA, NSAIDs, and antiplatelet agents can potentiate the effect
Heparin
Allergy to pork products may indicate a potential hypersensitivity
Heparin
Obtain daily weight for client on weight-based protocol
Heparin
normal adult dosage range of 20,000 to 40,000 units/24 hr
Heparin
Rotate injection location
Heparin
Not to be given in children b/c of association with Reye's syndrome
ASA
Use of these should be stopped for at least 7 days prior to a planned surgery
Antiplatelet meds
children, pregnant women, and lactating women should not take these
Antiplatelet meds
used in pregnancy only when benefit to mother outweighs risk to fetus
Antiplatelet meds
lactating women should be informed of risks to infant if this therapy is considered
Antiplatelet meds
Instruct client to wear Medic-alert bracelet
Antiplatelet meds
adequate fluid intake
Antiplatelet meds
can lead to iron deficiency anemia in female clients
ASA
Continuous monitoring of BP, mental status, and response to therapy should be documented
Thrombolytics
report any signs of chest pain, dizziness, headache or evidence of bleeding to health care provider
Thrombolytics
Place client on a cardiac monitor during administration
Thrombolytics
The antidote is aminocaproic acid (Amicar)
Thrombolytics
IM route for medication administration is contraindicated
Thrombolytics
Major side effect: Hemorrhage
Thrombolytics
Monitor client for vs changes, as there may be variations in pulse, BP and temp
Thrombolytics
Watch for signs of shock
Thrombolytics
Maintain adequate IV site for med admin; observe closely for s/s of infiltration
Thrombolytics
If client is found to be bleeding, med should be stopped; plasma or RBCs may be ordered
Thrombolytics
Monitor for dysrhythmias
Thrombolytics
Support client and family during acute-care management period
Thrombolytics
Administered via oral or IV route; close continuous monitoring of the client is required
Systemic hemostatics (aminocaporoic acid and tranexamic acid)
Contraindicated with coagulapathy (DIC), postpartum bleeding, upper urinary tract bleeding, or new burns
Systemic hemostatics (aminocaproic acid)
Food interactions: dietary sources of vitamin K
Systemic hemostatics
Monitor baseline labs r/t renal and liver function
Systemic hemostatics
Monitor PT levels and response to therapy
Systemic hemostatics (vitamin K)
Monitor coagulation profile for hypercoagulation
Systemic hemostatics
Rotate injection sites; assess for signs of local irritation
Systemic hemostatics (vitamin K)
Risk for volume overload
Systemic hemostatics
Use of dietary yogurt or buttermilk can help restore normal intestinal flora
Systemic hemostatics
Report difficulty urinating or reddish-brown urine while taking it
Systemic hemostatics (aminocaproic acid)
Report chest pain, arom or leg pain, or difficulty breathing
Systemic hemostatics
If client develops an allergic reaction to the product or if a reaction is anticipated, an antihistamine such as diphenhydramine (Benadryl) may be given
Local absorbable hemostatic agents
Switching from one material to another may facilitate a better response
Local absorbable hemostatic agents
Proper reconstitution and administration of the medication is required according to protocol
DDAVP
Document baseline vs during first 15 minutes of therapy and then according to protocol to monitor
DDAVP
Clients with defined factor deficiencies and their families will need anticipatory support and guidance during a lifetime of therapy
DDAVP
Clients who have hereditary factor antithrombin III deficiency ... are at risk for thrombosis
DDAVP
genetic transmission issues
DDAVP
Z-track admin required
Iron salts
Administered by straw to avoid discoloration of tooth enamel
Iron salts (with elixir)
Drug interactions: antacids, antibiotics, thyroid drugs
Iron salts
Decreased effect of tetracycline and penicillamine
Iron salts
Vitamin C can increase the absorption of oral med
Iron salts
Foods high in phytates (cereals) can cause decreased absorption
Iron salts
Not to be taken with milk
Iron salts
Lab studies: reticulocyte count
Iron salts
Dark and tarry stools
Iron salts
Give oral med on full stomach to minimize GI upset
Iron salts
Clients with GI surgeries that result in removal or anastomosis of the stomach and end the release of intrinsic factor will require these injections on a lifelong basis
Vitamin B12 (Cyanocobalamin)
Must be administered parenterally in clients who cannot manufacture intrinsic factor
Vitamin B12 (Cyanocobalamin)
Therapeutic level: Schilling test >30%
Vitamin B12 (Cyanocobalamin)
Rotate sites and use Z-track
Vitamin B12 (Cyanocobalamin)
protect from light
Vitamin B12 (Cyanocobalamin)
do not mix, give as separate injection
Vitamin B12 (Cyanocobalamin)
pernicious anemia
Vitamin B12 (Cyanocobalamin)
Food high in this: liver, kidney, fish, milk
Vitamin B12 (Cyanocobalamin)
Alcohol effects absorption
Vitamin B12 (Cyanocobalamin)
signs of deficiency: numbness and tingling in lower extremities, weakness, fatigue, anorexia, loss of taste, diarrhea, memory loss, and mood changes
Vitamin B12 (Cyanocobalamin)
If diarrhea significant, change in drug dosage may be required
Vitamin B12 (Cyanocobalamin)
Deficiency: neural tube defects in fetus
Folic acid
Deficiency: megaloblastic macrocytic anemia
Folic acid
Injections may contain benzyl alcohol
Folic acid
Injections not to be admin'd to neonates
Folic acid
Foods include: green leafy vegetables, yellow fruits and veg's, yeast, meats
Folic acid
Med is refrigerated, let warm to room temp before admin
Epoetin alfa (Epogen, Procrit)
Do not use med that is discolored or contains particulate matter
Epoetin alfa (Epogen, Procrit)
Do not shake, will lead to inactivation
Epoetin alfa (Epogen, Procrit)
no preservative, so must discard unused portion
Epoetin alfa (Epogen, Procrit)
Hematocrit indicates response (usu. 30-36%)
Epoetin alfa (Epogen, Procrit)
possible hypertension and seizures
Epoetin alfa (Epogen, Procrit)
Monitor for risk of thrombotic events
Epoetin alfa (Epogen, Procrit)
Clients on dialysis may requre adjusted dosages
Epoetin alfa (Epogen, Procrit)
Monitor iron stores
Epoetin alfa (Epogen, Procrit)
Premedicate if necessary with analgesics if bone pain is present or client becomes febrile
Epoetin alfa (Epogen, Procrit)
Do not drive or be involved in other hazardous activities during first 90 days of therapy
Epoetin alfa (Epogen, Procrit)
If no response in 3 months, notify prescriber
Fibric acid derivatives
Monitor closely for right upper quadrant (RUQ) pain or vomiting
Fibric acid derivatives
Restrict carb and alcohol intake
Fibric acid derivatives
Notify prescriber if acute appendicitis or gallbladder disease occur
Fibric acid derivatives
Report immediately unexplained bleeding
Fibric acid derivatives
Take early in the day to avoid nocturia
Loop diuretics, Thiazide diuretics, Potassium-sparing diuretics
Administer slowly as hearing loss can occur if injected rapidly
Loop diuretics (furosemide, Lasix IV)
Interaction with aminoglycosides causing ototoxicity
Loop diuretics
Monitor for electrolyte imbalance especially sodium and potassium
Loop diuretics
Monitor vs for s/s hypotension and tachycardia
Loop diuretics
Daily weights
All diuretics
I and O
All diuretics
Restrict Na intake; do not use salt substitutes if taking potassium supplement
Loop diuretics, Thiazide diuretics
Change position slowly to avoid orthostatic hypotension
Loop diuretics, Thiazide diuretics
Report ringing in ears immediately
Loop diuretics
Hypersensitivity to sulfonamide derivatives
Thiazide diuretics
May alter serum electrolytes, esp. lowering potassium
Thiazide diuretics
Electrolyte imbalance, impaired glucose tolerance, jaundice, muscle cramps, photosensitivity, impotence, and hyperuricemia
Thiazide diuretics
Dizziness, vertigo, headache, and weakness
Thiazide diuretics
Dehydration, orthostatic hypotension,nausea and vomiting, abdominal pain, diarrhea, constipation, and freq urination
Thiazide diuretics
Dermatitis and rash
Thiazide diuretics
Assess indicators of dehydration: thirst, poor skin turgor, coated tongue
Thiazide diuretics
Avoid salt substitutes
Potassium-sparing diuretics
Contraindicated with serum levels greater than 5.5 mEq/mL
Potassium-sparing diuretics
Contraindications: anuria, acute and chronic renal insufficiency, diabetic nephropathy, hypersensitivity, and impaired hepatic function
Potassium-sparing diuretics
May potentiate hypotensive effects of antihypertensives
Potassium-sparing diuretics
Increased risk of hyperkalemia with other like meds
Potassium-sparing diuretics
Monitor electrolytes (especially) potassium, creatinine, and BUN
Potassium-sparing diuretics
Adverse effects/toxicity: Hyperkalemia
Potassium-sparing diuretics
Monitor vs and I&O
Potassium-sparing diuretics
Monitor for nausea, diarrhea, abdominal cramps, and tachycardia followed by bradycardia
Potassium-sparing diuretics
Triamterene may turn the urine blue
Potassium-sparing diuretics
Contraindications: narrow angle or acute glaucoma
Diamox
Adverse effect/toxicity: Thrombocytopenia purpura, hemolytic anemia, leukopenia, pancytopenia, and agranulocytosis
Diamox
Do not take aspirin
Diamox
Be aware of and avoid high-sodium foods and beverages; eat food high in potassium instead
Diamox
Used to decrease intracranial or intraocular pressure
Osmotic diuretics
Mannitol crystallizes at low temperatures
Osmotic diuretics
Adverse effects/toxicity: Thrombophlebitis
Osmotic diuretics
Adverse effects/toxicity: CHF
Osmotic diuretics
Report immediately pain in chest or legs, shortness of breath, or apnea
Osmotic diuretics
Tablet form should be taken with full glass of water
Potassium supplements
Powder form should be mixed with 4 ounces of water or other liquid
Potassium supplements
Should be taken with meals to decrease GI irritation
Potassium supplements
Parenterally should be given slowly, even with central line
Potassium supplements
Contraindications: severe renal impairment with oliguria, anuria, or azotemia
Potassium supplements
Use with potassium-sparing diuretics, ACE inhibitors or salt substitutes can cause sever hyperkalemia
Potassium supplements
Food interactions: apple juice, grapefruit, banans, oranges, peaches, pears, raisins, broccoli, peas, tomatoes, eggplant, chicken, liver, turkey, salmon, beef, low-fat yogurt, milk, and chocolate milk
Potassium supplements
Adverse effects/toxicity: dysrhythmias or cardiac arrest
Potassium supplements
Adverse effects/toxicity: Respiratory paralysis
Potassium supplements
Monitor side effects such as weakness, feeling of heaviness in legs, confusion, hypotension
Potassium supplements
Should not be given immediately postoperatively until urine flow is established
Potassium supplements
Report diarrhea or vomiting b/c of increased risk for hypokalemia
Potassium supplements
Monitor stools for evidence of blood
Potassium supplements
May cause syncope within 30 minutes to 1 hour after first dose; effect is transient and may be diminished by giving at bedtime
Alpha and alpha/beta blockers
monitor apical pulse for increased risk of bradycardia; signs of hypoglycemia may be masked
Beta-blockers
Side effects: first dose syncope, headache, drowsiness, hypotension, palpitations, impotence, nasal congestion, n/v, tachycardia
Alpha-blockers
Side effects: fatigue, orthostatic hypotension, dizziness, n/v, diarrhea, bronchospasm, muscle spasm, transient scalp tingling, hyperglycemia, upper respiratory infections, impotence, and arthralgias
Alpha/beta blockers
Side effects: heart failure, agranulocytosis, bronchospasm
Beta blockers
Interactions: potassium-sparing diuretics or potassium supplements (hyperkalemia)
ACE inhibitors
Side effects: n/v, abdominal pain, constipation, persistent dry nonproductive cough, and dyspnea
ACE inhibitors
Adverse effects/toxicity: angioedema, leukopenia, agranulocytosis
ACE inhibitors
Take BP before giving dose and monitor regularly
ACE inhibitors
Report peripheral edema, signs of infection, facial swelling, loss of taste, or difficulty breathing
ACE inhibitors
Do not skip dose or stop taking drug; may cause serious rebound BP
ACE inhibitors
Notify provider if persistent, dry cough occurs
ACE inhibitors
Side effects: hypotension and dizziness, cough, GI upset, insomnia, nasal congestion or pharyngitis, myalgia/arthralgia, flu-like symptoms
Angiotensin II antagonists
Monitor client taking diuretics for additive hypotension
Angiotensin II antagonists
Notify prescriber immediately if pregnancy is suspected
Angiotensin II antagonists
Use nonhormonal birth control methods
Angiotensin II antagonists
Withhold medication if BP less than 90/60
Calcium channel blockers
Do not take with grapefruit, may increase drug level and adverse effects
Calcium channel blockers
Side effects: constipation (esp w/ oral and sustained-release forms)
Calcium channel blockers
Side effects: postural hypotension
Calcium channel blockers
Evaluate BP and ECG before initiation of treatment and monitor them closely during medication adjustment
Calcium channel blockers
Take radial pulse before each dose; report irregular pulse or pulse slower than base level
Calcium channel blockers
Increase renal blood flow directly
Vasodilators
Headache and palpitations may occur 2-4 hours after the first dose and should subside spontaneously
Vasodilators
Monitor BP and apical pulse regularly
Vasodilators
Headache, palpitations, and rapid pulse may occur but should be gone in about 10 days
Vasodilators
Side effects: bradycardia, orthostatic hypotension, aggravation of angina, edema
Anti-adrenergic meds (Other antihypertensives)
Transdermal systems are applied to dry, hairless areas on skin of chest or upper
Anti-adrenergic meds (Other antihypertensives)
[Clonidine]
Restrict sodium if ordered and lost weight as needed; report weight gain of greater than 5 lb per week
Anti-adrenergic meds (Other antihypertensives)
Relieve dry mouth by sipping water or chewing sugarless gum
Anti-adrenergic meds (Other antihypertensives)
Do not drive care or perform hazardous activities if drug causes drowsiness
Anti-adrenergic meds (Other antihypertensives)
Do not administer solutions that have darkened or contain particle matter
Meds for hypertensive emergencies
Intravenous infusion titrated to BP
Meds for hypertensive emergencies
IV is given undiluted by rapid direct IV injection over 10-30 seconds
Meds for hypertensive emergencies
[Diazoxide]
Client should be recumbent while receiving IV and should remain in bed for at least 30 minutes following administration
Meds for hypertensive emergencies
A diuretic should be prescribed to prevent CHF after administering med since it causes sodium and water retention
Meds for hypertensive emergencies
[Diazoxide]
Side effects: dizziness, weakness, headache, malaise, flushing, palpitations, insomnia, paresthesia, arrhythmia, tachycardia, hypotension, angina, diaphoresis
Meds for hypertensive emergencies
Side effects: Sodium and water retention, visual disturbances, GI disturbances, azotemia, decreased urinary output, rash
Meds for hypertensive emergencies
Adverse effects/toxicity: Thrombocytopenia, increased intracranial pressure, thiocyanate toxicity, methemoglobinemia, cyanide toxicity
Meds for hypertensive emergencies
Monitor BP every 5 minutes for 15-30 minutes, then hourly until client is stable
Meds for hypertensive emergencies
Check thiocyanate levels every 72 hours
Meds for hypertensive emergencies
Monitor blood glucose levels, esp diabetic clients
Meds for hypertensive emergencies