Pharma Test 3 Flashcards

1
Q

Anticoagulant Drugs

A
  • Heparin, a naturally occurring anticoagulant, is produced by mast cells located in connective tissue throughout the body.
  • All anticoagulants interfere with the clotting cascade and prolong blood clotting time.
  • The parenteral anticoagulants work by preventing the conversion of fibrinogen to fibrin.
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2
Q

Heparin

A
  • Rapidly promotes the inactivation of factor III, which, in turn, prevents the conversion of prothrombin to thrombin and fibrinogen to fibrin. (Stops clots from forming)
  • ½ life of 90 min. short-acting!
    -SE: Heparin-induced thrombocytopenia, hep is made from pigs and protein produced in body so can develop an allergy to it.
  • NC: Monitor aPTT(1.5-2.5 x 30-40 secs), give loading dose then infuse, has no effect on clots already formed
  • Antidote: protamine sulfate(base anticoagulant)
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3
Q

enoxaparin (Lovenox

A
  • Low Molecular Weight heparin (Half-life: 4.5 hr)
  • no need for serum PTT’s (works on factor X, not thrombin)
  • Black Box Warning for spinal procedures
  • No antidote! Protamine sulfate has been used with limited success
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4
Q

Warfarin (Coumadin)

A
  • Oral Anticoagulant and made from natural chemical= Dicoumarol from rotting clover
  • Used for decades to kill rodents in food warehouses.
  • Work by preventing the synthesis of factors dependent on vitamin K for synthesis.
  • Pts with long term risk for thrombus formation
  • Long-acting and takes a few days to work and get out of your system. (Half life 0.5 - 3 days)
  • Blocks Vitamin K at its sites of action so Pt overloaded with Vitamin K on Warfarin-> blood clots in the legs
  • NC: Dose should be individualized until PT or the INR is in the therapeutic range.INR (International Normalized Ratio) therapeutic range for treatment = 2-3(lower 2= blood to thick, 3= blood to thin), No Vitamin K rich foods
  • Antidote= Vitamin K (phytonadione)
  • When transitioning from heparin to warfarin, the two drugs must be administered concurrently for 2-3 days.
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5
Q

Rivaroxaban (Xarelto)

A
  • DVT/ PE treatment and prophylaxis, Afib/flutter thrombus prophylaxis
  • Inhibits the formation of thrombin by blocking factor Xa
  • Half-life: 5–9 hr
  • No pts with valvular dysfunction or mechanical valve, epidural/spinal puncture
  • NC: Monitor or bleeding, LOC, no antidote, monitor Cr+, must be off for at least 48 hrs prior to surgery, $15/pill, Monitor BUN and Creatinine(Kidney function and clear the drug in a timely manner), DO NOT HAVE TO MONITOR PT, aPPT, OR INR!
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6
Q

Antiplatelet Drugs

A
  • They are used when overactive platelets pose long-term risks for hypercoagulability.
  • Antiplatelet drugs reduce platelet aggregation.
  • Prototype drug: clopidogrel (Plavix).
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7
Q

Clopidogrel

A
  • Used to reduce atherosclerotic events. (post MI or CVA especially)
  • Stop the binding of adenosine diphosphate (ADP) binding to its platelet receptor and the subsequent ADP-mediated activation of the glycoprotein IIb/IIIa complex, thus inhibiting platelet aggregation.
  • Half-life: 6 hr
  • SE: Neutropenia and GI distress, GI bleeding(most serious)
  • Many times put on an H2 blocker preventatively and not a PPI bc PPI decrease therapeutic effect
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8
Q

Thrombolytic drugs

A
  • Break down formed clots
  • Pts who are diagnosed with an evolving, acute MI; a PE; or acute ischemic stroke.
  • May be given to unclog central venous catheters.
  • May be given systemically or directly at the blood clot site.
  • Adverse effects can be life threatening.
  • Prototype drug: alteplase (Activase; Cathflo Activase)
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9
Q

Alteplase Recombinant

A
  • Rapidly cleared from the plasma ½ life 5-10 min
  • Acts the same as tPA and Converts plasminogen to plasmin, leading to breakdown of the clot.
  • Vital signs, evidence of bleeding, and laboratory test results should be assessed throughout therapy
  • NC: Monitor for signs and sx of bleeding (petechia, sudden severe HA, LOC, joint swelling, drop in b/p with increase in HR), Know the ½ life of anticoagulants, Monitor platelets , Hmg/Hct, coagulation studies
  • Aminocaproic acid (Amicar) may be used as an antidote.
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10
Q

Erythropoiesis-stimulating drug

A
  • Epoetin alfa is made through recombinant D N A technology and is functionally identical to human erythropoietin.
  • Prototype Drug: Epoetin Alfa (Epogen, Procrit)
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11
Q

Epoetin Alpha (Epogen, Procrit)

A

-Renal failure(kidneys cant make it anymore), chemotherapy treatments(destroys RBC), blood loss, and anemia
-Stimulates bone marrow to make RBC
-SE:serious cardiovascular and thrombolytic events(clots, strokes, MI) , HTN(increasing volume of blood and osmotic pole of fluids)
-No pts with hypersensitivity to mammalian cell products (rodents; hamsters; mice)
-Interacts with Androgen (hormone) therapy(Increase thrombolic events )

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12
Q

Colony-Stimulating Factors (CFS)

A

-Increase the production of new leukocytes and activate existing white blood cells
-Prototype Drug: Filgrastim (Granix, Neupogen)

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13
Q

Filgrastim (Granix, Neupogen)

A
  • Neutropenia primarily in cancer treatment or after chemotherapy
  • Stimulates hematopoietic cells to produce and activate neutrophils
  • SE:Bone pain(affecting bone marrow), neutropenic fever(KNOW; Common; give unless fever 105F)
  • No pts with hypersensitivity to E. coli proteins because this microbe is used to produce the recombinant drug.
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14
Q

Cyanocobalamin (Nascobal)

A
  • Vitamin B12 for Anemia(Pernicious anemia, megaloblastic anemia)
  • PO if intrinsic factor present to make the B12 active
  • Pts with Dumping Syndrome need the med to administered Nasal or SQ
  • Few SE but will turn urine a bright yellow
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15
Q

Ferrous Sulfate(Feosol)

A
  • Iron deficiency anemia
  • Provides the iron molecule essential to formation of RBCs and hemoglobin.
  • SE: GI upset, constipation and may darken stools(black but not tarry)
  • Antidote= Deferoxamine (Desferal)a parenteral agent that binds iron, which is subsequently removed by the kidneys, turning the urine a reddish-brown color(iron coming out).Primarily used in pediatrics bc flinstone vitamins taste good
  • NC: Don’t shake vial bc may deactivate the drug for CFS. Dont send via tube system and walk it back if you return it. This drug is expensive. Monitor CBC count(Leukocytes greater than 100,000 can cause respiratory failure, intracranial hemorrhage, retinal hemorrhage, and MI)
  • Iron Administration: Use the Z-track method (deep muscle) when giving IM(if not will come oozing out and can stain the skin where it looks like a bruise), Do not crush tablets or empty contents of capsules when administering, Do not give tablets or capsules within 1 hour of bedtime bc can cause GI upset, PO Give on empty stomach or with high acid food to help absorb iron better (Vitamin C= Orange juice, Kiwi), MOnitor for toxicity and local tissue irritation if IV(SOB, seizures, hypotension)

-

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16
Q

Hydrochlorothiazide

A
  • Thiazide Diuretics
  • Used in the treatment of HTN (decrease blood volume) and edema
  • Acts in the distal tubule by ncreasesing excretion of sodium and chloride in the distal convoluted tubule thereby taking water with it (trades it out with potassium). Weaker diuretic(Water goes with it bc water goes with sodium)
  • SE:Hypokalemia, hyponatremia, hypochloremia, and hypercalcemia
  • Wont be on potassium supplements
  • watch electrolytes bc sometime pts wont hold on to their sodium and most of the time they do
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17
Q

Loop Diuretics

A
  • The loop diuretics work in the loop of Henle to inhibit reabsorption of sodium and chloride.
  • Exert a powerful effect on fluid and electrolyte balance.
  • Referred to as high-ceiling(more you give, the more it works) diuretics because the maximum diuretic effect that can be achieved is higher than with other diuretics.
  • Prototype drug: furosemide (Lasix)
  • Bumetide (Bumex)- more potent; Torsemide (Demadex)- longer duration
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18
Q

Furosemide

A
  • Used to treat peripheral & pulmonary edema & HTN.
  • Highly protein-bound drug so If pts are malnourished-> can have toxic effects-> make sure to have albumin on board
  • Inhibits the reabsorption of sodium-, chloride, and water in the ascending loop of Henle.(Trades potassium out for sodium)
  • SE: Electrolyte imbalance (especially K+ and Mg), alterations in glucose
  • NC:Doses over 80 mg IVP can be ototoxic. Pushing too fast can cause subclavian pain and ototoxicity, Damage to the nerve to the inner ear if given too much or too fast, Ear ringing on the side of the IV that ur pushing med in
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19
Q

Potassium-Sparing Diuretics

A
  • Promote sodium and water excretion in the distal tubule.
  • At the same time, potassium is not excreted; rather, it is reabsorbed to make up for the ion exchange.
  • Produces weak diuresis and antihypertensive effects when used alone.
  • Pts taking potassium-sparing diuretics are at risk for developing hyperkalemia.
  • Also aldosterone blocker
  • Prototype drug: Spironolactone (Aldactone)
20
Q

Spironolactone

A
  • Used as an adjunct to manage HF, edema, and hypertension.
  • Inhibiting transport of sodium in the distal tubules back into the blood stream independent of aldosterone.
  • No pts with renal or liver disease
  • SE: Hyperkalemia, nephrotoxicity, thrombocytopenia, elevated liver enzymes,and photosensitivity
    *
21
Q

Albumin (Albuminar)

A
  • Blood product/Colloid volume expander
  • Tx: Shock, hypoproteinemia, “3rd spacing”
  • Large proteins that draw fluid into the vascular space(bloodstream)-> Increasing BP and osmotic pressure
  • NC: Monitor for rapid fluid shift( Pulmonary edema, Lung sounds (crackles), SOB,coughing), and religious prefernces
22
Q

Beta-adrenergic agonists

A
  • Mimic the action of the SNS.
  • Beta-adrenergic agonists are also labeled according to their selectivity.
  • Prototype: (nonspecific) dopamine (Intropin)
23
Q

Dopamine

A
  • Tx: shock, 2nd degree MI, trauma, sepsis, CHF, surgery, renal failure
  • timulates alpha-1 and beta-1 and dopaminergic receptors: increased cardiac output at higher dose- above 5 mcg/kg/min
  • No pts with PVC’s or Pheochromocytoma
  • IV dopamine does not work with parkinsons because it does not cross the BBB
  • Correct any acidosis (dec. effectiveness)-> in order for the dopamine to work properly bc PH not compatible with the way the drug works.
  • SE: hypotension, ectopic beats, N/V
  • Extravasation treatment: phentolamine(adrenergic blocker) if dopamine seeps underneath subcutaneous tissue bc it begins to clamp down circulation to blood vessels, killing tissues.
24
Q

Adrenergic Agonist

A
  • Adrenergic agonists are drugs that mimic the action of the SNS.
  • Classified according to their selectivity.
  • Non-selective adrenergic agonists stimulate both alpha and beta receptors.
  • Prototype drug: nonselective adrenergic agonist epinephrine
25
Q

Epinephrine

A
  • Tx: asthma, shock, CPR, resp. failure, anaphylaxis
  • ICU= parenterally. CPR use if there is no IV access and can give down a endotracheal tube.
  • Stimulates all adrenergic alpha and beta receptors
  • No pts with closed-angle glaucoma or during child labor
  • SE: hypertensive crisis, angina, cerebral hemorrhage, and cardiac arrhythmias.
26
Q

Norepinephrine D (Levophed)

A
  • Tx: shock (especially septic), cardiac arrest
  • Stimulates alpha and to a lesser degree beta1 receptors and causes vasopressor and some inotropic effects. Nonselective vasopressor.
  • Not causing the heart to work as hard as epi and same contraindications as epi
  • SE: hypertensive crisis, angina, cerebral hemorrhage, reflexive bradycardia, and cardiac arrhythmias.
  • Extravasation treatment- phentolamine (adrenergic blocker)
  • NC: Fluid replacement is a priority before vasopressors for shock, Monitor LOC and B/P (preferably with an invasive arterial line), LOC could indicate brain damage, IV infusion should be a central line, Weaning should be done with all adrenergic drugs do not stop abruptly(Paradoxical effect if you dont wean pt-> BP will be lower than before they started on levo.), Increased urine output is indicative that shock treatment is working and good perfusion thru da body
27
Q

Which drugs are best for shock?

A

Sympathetic drugs such as dopamine

28
Q

Posterior pituitary gland dysfunction:

A
  • major disorders are diabetes insipidus (DI) and syndrome of inappropriate antidiuretic hormone (SIADH).
29
Q

Posterior Pituitary Hormone Regulators

A
  • Stores two hormones that are produced in the hypothalamus: vasopressin and oxytocin.
  • Desmopressin and vasopressin are synthetic drugs of the naturally occurring posterior pituitary hormone.
  • Prototype drug: desmopressin (DDVAP
30
Q

Desmopressin

A
  • Manage central DI and nocturnal enuresis (bed wetting), hemophilia A and von Willebrands’ disease(has blood clotting enhancement)
  • Synthetic hormone vasopressin increases clotting factor production, vasconstriction of blood vessells and causes the kidney to retain or reabsorb water back into circulation.
  • SE: Transient headache, nasal problems, Fluid overload, hyponatremia
  • NC: Monitor fluid status(weight, b/p, Na+), watch for water toxicity(dilutes sodium to a dangerous level).
31
Q

Thyroid drugs

A
  • Treat hyperthyroidism or hypothyroidism.
  • Hyperthyroidism= Metabolism in overdrive( Weight loss, tachycardia, sweating, insomnia, high BP)
  • Hypothyroidism= Slowed down( hypotension, cold, weight gain, sluggish, cant think very well.)
  • The only treatment for hypothyroidism is lifelong replacement of thyroid hormones.
  • Prototype drug: levothyroxine (T4; Levothroid, Synthroid); it is synthetic and given in micrograms
32
Q

Armour Thyroid

A
  • Tx hypothyroidusm
  • Natural T3 and T4 hormone from the thyroid of pigs
  • Given in milligrams. Worried about allergies such as pigs.
33
Q

Levothyroxine

A
  • Acts as replacement for natural T4 thyroid hormone in hypothyroidism.
  • No pts with acute MI complicated by hypothyrodism(Will test recent MI pts to see if their thyroid had something to do with MI. Can make the MI and heart worse. )
  • Can be given IV in a crisis
  • SE: Signs of Hyperthyroidism(HTN, tachycardia, headache, heat inltolerance)
  • NC: HR and B/P are essential to monitor, TSH is the lab to evaluate for effectiveness, takes 1-3weeks for full effectiveness. Must be taken on a empty stomach!, Toxicity resembles a thyroid stormand can be life threatening->Can cause HF,
  • TSH is low->hyperthyroidism and vice versa. More thyroid med if TSH is high to stop TSH from stimulating the thyroid.Not giving enough thyroid med which causes the body to continue stimu
  • If pt has a high TSH adjust thyroid medication
34
Q

Antithyroid Compounds (Thionamides)

A
  • Hyperthyroidism is treated with thyroid-hormone antagonist drugs, surgery, or radioactive iodine.
  • The purpose of treatment is to reduce the amount of functional thyroid tissue.
  • Prototype drug: propylthiouracil (PTU
35
Q

Propylthiouracil

A
  • Palliative treatment of hyperthyroidism or adjunct to radiation therapy, or stabilization while awaiting thyroidectomy. Short term use till long lasting tc
  • Inhibits the synthesis of thyroid hormones, prevents oxidation of iodide, and blocks conversion of T4 into T3.
  • No prego pts can cause miscarriage
  • SE: Liver failure, agranulocytosis, altered taste sensation, athralgia, vertigo
36
Q

Adrenal drugs (Corticosteroids)

A
  • The primary endogenous glucocorticoids produced by the adrenal gland are cortisol (hydrocortisone) and cortisone.
  • Our natural cortisol are debleated with prolonged stressors such as chronic illness
  • Supports minerals in blood stream, prolonged stress or traumatic illness -> causes adrenal glands to shrink which reduces the production of steroids. Which leads to a disruption of minerals.
  • Prototype drug: hydrocortisone (Cortef)
37
Q

Hydrocortisone

A
  • Replacement therapy for adrenal insufficiency, inflammation, allergic reactions, and anti-inflammatory for joint injections
  • Replaces the body’s own cortisol and inhibits multiple inflammatory cytokines.
  • No pts with DM, osteoprosis, psychosis, or hypothyrodism
  • SE: Cushingoid syndrome, psychosis, depression, insomnia
  • NC: Will cause hyperglycemia in both DM and Non-DM pt., increases Na+, Ca++, cholesterol. Decreases K+(monitor EKG)
38
Q

Diabetes

A
  • Type 1= autoimmune -> destruction of insulin secreteing beta cells in pancreas
  • Type 2= insulin resistance by tissues
  • Synthetic insulin (exogenous) acts in the same manner as endogenously produced insulin.
  • Sources of synthetic insulin= pork and beef panceas, now its recombinant DNA or gentic energineering to create human like insulin
39
Q

Regular Insulin

A
  • All types of DM
  • Only IV that can be used IV
  • Mimics the effect of human insulin
  • Works by transporting glucose across cell membrane, converts glucose into glycogen, decrease glucose by taking insulin in cell which is done w/ K
  • High K+ pts will get inuslin to decrease potasium
  • Monitor K+ closely in diabetic patients.
  • beta blockers(blocks the symp of hypoglycemia)
40
Q

Non Sulfonylureas

A
  • Comprise three different classes grouped by their chemical structure: biguanides, thiazolidinediones, and alpha-glucosidase inhibitors.
  • Mode of action: Improve insulin action and delay the digestion of carbs
  • Prototype drug: metformin (Fortamet, Glucophage)
41
Q

Metformin

A
  • Adjunct to therapy to lower blood glucose in type 2 diabetes.
  • Decreases hepatic glucose production, decreases intestinal absorption of glucose from food, and improves insulin sensivitivty by increasing peripheral glucose uptake.
  • Works on the intestines and decreasest the aborsption of carbs
  • No pts with Hepatic disease (increased risk of lactic acidosis or metabolic acidosis)
  • SE: flautence, diarrhea and metallic sensation(Delays bowel from doing its job-> bacteria will ferment-> extra gas and discomfort)
  • May react with contrast media used for radiographic procedures, hold for 24-48 hrs(48 hrs ideally) before and after! Causes renal failure(fry kidneys) and lactic acidosis.
  • NC: Inslulin pumps only contain short acting, Point of care BS must be done within 1 hr of administering insulin, Illness, stress, and exercise all change inulin/carb requirements(Exercise helps lower BG. May have more hypoglycemic events),
42
Q

Vaccines

A
  • Artificial exposure to antigens use to stimulate the immune system to produce antibodies to produce immunity
  • Can be live vaccines or attenuated mean (weakened or dead)
  • Creates active immunity to diseases
  • Prototype: Hepatitis B
43
Q

Hepatitis B: Vaccine

A
  • provides active immunity agt blood born disease and in individuals who are at risk for exposure to hepatitis B virus (H B V) such as health care workers, dental ppl, morticians, and paramedics and standard for all infants.
  • 3 IM shots: the second dose is given 1 month after the first, and the third dose 6 months after the first dose.
  • Given to children: at birth, at 1–4 months, and 6–18 months later
  • Attenuated vaccine of hepatitis B antigen (protein) that stimulates the immune system
  • Produced through recombinant D N A technology using yeast cells.
  • Common reaction to vaccine is anaphlyaxis so Epinephrine (1:1,000)
  • No pts with Immunosuppression therapy
44
Q

Immunostimulants

A
  • Interferons (IFNs) and interleukins (ILs)= stimulates immune system to respond to something; warns other cells something is going on and increases activity of WBC
  • Boost patient’s immune system
  • Used to treat certain viral infections, immunodeficiencies, and specific cancers
  • Secreted by lymphocytes and macrophages that have been infected with a virus
  • Slow spread of viral infections and enhance activity of leukocytes
  • Prototype Drug: Interferon alfa-2b
45
Q

Interferon alfa-2b

A
  • Treat Cancers(MM, non hodgkin’s lymphoma, AIDS- related Kaposi sacroma), Viral infections(HPV, Hep B and C)
  • SE:dizzy(expected), hepatotoxicity, neurotoxicity, SI
  • No pts with hepatic issues
  • NC: Monitor and report fevers over 101, instruct pt to rise slowly to prevent dizziness. Injection site may become redden. Causes increased release of cytokines(body feel bad after infection not bc of the medicine)
46
Q

Immunosuppressants

A
  • Inhibit patient’s immune system
  • Toxic to bone marrow (must monitor CBC’s)
  • Increased risk of infections and lymphoma
  • Immunosuppressant classes are Corticosteroids, Antimetabolites, Antibodies, and calcineurin inhibitors
47
Q

Cyclosporine (Gengraf, Neoral)

A
  • Tx: Psoriasis, organ transplant, UC or Crohn’s, RA
  • Bind to calcineurin and disrupt Tc ells
  • Watch out for the antigen(Stops the immune system from reacting to make sure body is not rejecting new organ)
  • Only chemo certified nurses or hcp in immunosupressive thearpy admin this medication
  • SE: Low urine output, gingival hyperplasia, and elevated hepatic enzymes
  • NC: Monitor renal function, CBC, S/S of infection since these can be masked during immunosupression. Typically wont run a fever since immune system is being blocked from reacting.Protect pt and teach pt how to protect from others that are contagious and while in large public gatherings. Avoid crowds and must wash hands