1. Antihypertensives Flashcards

(50 cards)

1
Q

Norvasc™

Pharmacologic Category

A

Amlodipine

Calcium Channel Blocker

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2
Q

Norvasc™

FDA Approved Indications/Uses

A

Amlodipine

  • Coronary Artery Disease (CAD)
  • Hypertension (HTN)
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3
Q

Norvasc™

Adverse Effects

A
  • Abdominal pain
  • Dizziness
  • Fatigue
  • Flushing
  • Headache
  • Nausea
  • Palpitations
  • Peripheral edema
  • Somnolence
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4
Q

Norvasc™

Dosage Forms

A
  • Tablets
    • 2.5mg
    • 5mg
    • 10mg
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5
Q

Norvasc™

Patient Education

A
  • Patient should avoid activities requiring coordination until drug effects are realized, as drug may cause dizziness.
  • Instruct patient to report signs/symptoms of exacerbation of angina or myocardial infarction with initiation and increase in dose.
    • Patients with severe cardiovascular disease have an increased risk.
  • Instruct patient to take a missed dose as soon as possible, but if it has been more than 12 hours since the dose was missed,
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6
Q

Tenormin™

Pharmacologic Category

A

Atenolol

Beta Blocker

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7
Q

Tenormin™

FDA Approved Indications/Uses

A

Atenolol

  • Acute Myocardial Infarction
  • Angina
  • Hypertension (HTN)
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8
Q

Tenormin™

Adverse Effects

A

Atenolol

  • Bradyarrhythmia
  • Cold extremities
  • Depression
  • Dizziness
  • Fatigue
  • Hypotension
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9
Q

Tenormin™

Dosage Forms

A

Atenolol

  • Tablet:
    • 25mg
    • 50mg
    • 100mg
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10
Q

Tenormin™

Patient Education

A

Atenolol

  • Patient should avoid activities requiring mental alertness or coordination until drug effects are realized, as drug may cause dizziness.
  • Advise patient to report signs/symptoms of cardiac failure.
  • Advise patient against sudden discontinuation of drug especially when being treated for angina.
    • Abrupt withdrawal may cause rebound angina.
  • Patient should take drug on an empty stomach
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11
Q

Coreg™

Pharmacologic Category

A

Carvedilol

Alpha-/Beta-Adrenergic Blocker

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12
Q

Coreg™

FDA Approved Indications/Uses

A

Carvedilol

  • Hypertension (HTN)
  • Heart failure
  • Impaired left ventricular fusion—myocardial infarction (MI)
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13
Q

Coreg™

Adverse Effects

A

Carvedilol

  • Bradyarrhythmia
  • Hypotension
  • Peripheral edema
  • Abnormal weight gain
  • Hyperglycemia
  • Diarrhea
  • Dizziness
  • Erectile dysfunction
  • Fatigue
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14
Q

Coreg™

Dosage Forms

A

Carvedilol

  • Tablet
    • 3.125mg
    • 6.25mg
    • 12.5mg
    • 25mg
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15
Q

Coreg™

Patient Education

A

Carvedilol

  • Patient should avoid activities requiring coordination until drug effects are realized, as drug may cause dizziness.
  • This drug may cause diarrhea, nausea, vomiting, arthralgia, back pain, myalgia, headache, vision disorder, erectile dysfunction, reduced libido, or fatigue.
  • Instruct patient to report signs/symptoms of adverse cardiovascular effects such as hypotension (especially in elderly patients), arrhythmias, syncope, palpitations, angina, or edema.
  • Drug may mask symptoms of hypoglycemia. Advise diabetic patients to carefully monitor blood sugar levels.
  • Patient should take drug with food.
  • Advise patient against sudden discontinuation of drug.
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16
Q

Cardizem™

Pharmacologic Category

A

Diltiazem

Calcium Channel Blocker

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17
Q

Cardizem™

FDA Approved Indications/Uses

A

Diltiazem

  • Atrial arrythmia
  • Hypertension
  • Paroxysmal supraventricular tachycardia
  • Stable angina, chronic
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18
Q

Cardizem™

Adverse Effects

A

Diltiazem

  • Bradyarrhythmia
  • Peripheral edema
  • Dizziness
  • Headache
  • Cough
  • Fatigue
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19
Q

Cardizem™

Dosage Forms

A

Diltiazem

  • Tablet
    • 30mg
    • 60mg
    • 90mg
    • 120mg
  • ER Tablets
    • 180mg
    • 240mg
    • 300mg
    • 360mg
    • 420
  • Capsules
  • IV
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20
Q

Cardizem™

Patient Education

A

Diltiazem

  • Patient should avoid activities requiring coordination until drug effects are realized, as drug may cause dizziness.
  • This drug may cause gingival hyperplasia, headache, or dermatologic reactions such as exfoliative dermatitis (reddened skin, skin peeling/flaking) or erythema multiforme (flu-like symptoms, spreading red rash, may progress to more severe form with blistering).
  • Instruct patient to report symptomatic hypotension, bradyarrhythmia, peripheral edema, or syncope.
  • Advise patient against sudden discontinuation of drug.
  • This drug is available in multiple brand names with varying properties by brand. Instruct patient to follow administration instructions specific to the prescribed brand with regards to meals and timing.
  • Patient should avoid concomitant use of beta-blockers or digitalis during drug therapy, unless otherwise directed by healthcare professional.
  • Patient should not drink alcohol while taking this drug.
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21
Q

Lasix™

Pharmacologic Category

A

Furosemide

  • Diuretic
  • Anthranilic Acid Derivative
22
Q

Lasix™

FDA Approved Indications/Uses

A

Furosemide

  • Congestive heart failure – edema
  • Edema
  • Renal failure – edema
  • Hypertension
  • Pulmonary embolism, acute; adjunct
23
Q

Lasix™

Adverse Effects

A

Furosemide

  • Hyperuricemia
  • Hypomagnesemia
  • Loss of appetite
  • Spasm of bladder
24
Q

Lasix™

Dosage Forms

A

Furosemide

  • Tablet
    • 20mg
    • 40mg
    • 80mg
25
Lasix™ Patient Education
Furosemide * Drug causes sun-sensitivity. Advise patient to use sunscreen and avoid tanning beds. * Patient should avoid activities requiring coordination until drug effects are realized, as drug may cause dizziness, vertigo, or blurred vision. * This drug may cause hyperglycemia, hyperuricemia, constipation, diarrhea, loss of appetite, nausea, vomiting, purpuric disorder, cramps, spasticity, asthenia, headache, paresthesia, or scaling eczema. * Instruct patient to report unusual bleeding/bruising or signs/symptoms of hypotension, infection, pancreatitis, or ototoxicity (tinnitus, hearing impairment). * Advise patient to report signs/symptoms of a severe skin reactions (flu-like symptoms, spreading red rash, or skin/mucous membrane blistering) or erythema multiforme. * Instruct patient to eat high-potassium foods during drug therapy, as directed by healthcare professional. * Patient should not drink alcohol while taking this drug.
26
Microzide™ Pharmacologic Category
Hydrochlorothiazide Diuretic
27
Microzide™ FDA Approved Indications/Uses
Hydrochlorothiazide * Edema; adjunct * Hypertension
28
Microzide™ Adverse Effects
Hydrochlorothiazide * Hypotension * Phototoxicity * Vertigo
29
Microzide™ Dosage Forms
Hydrochlorothiazide * Capsule * 12.5mg * Tablet * 12.5mg * 25mg * 50mg
30
Microzide™ Patient Education
Hydrochlorothiazide * Warn patient to avoid activities requiring mental alertness or coordination until drug effects are realized, as drug may cause blurred vision, vertigo, or dizziness. * Drug may cause electrolyte imbalances (hyperuricemia, hyponatremia, hypercalcemia), constipation, diarrhea, nausea, vomiting, paresthesias, muscle spasm, photosensitivity, rash, restlessness, or impotence. * Advise patient to report signs/symptoms of acute transient myopia associated with acute angle-closure glaucoma, including sudden ocular pain or decreased visual acuity. * Counsel diabetic patient to monitor for signs/symptoms of hyperglycemia and to report difficulties with glycemic control. * Tell patient to maintain adequate hydration, especially with exercise, sweating, diarrhea, or vomiting. * Advise patient to report signs/symptoms of hypotension, hypokalemia, or hypomagnesemia. * Instruct patient to avoid alcohol while taking drug as orthostatic hypotension may be aggravated. * Warn patient that there are multiple significant drug-drug interactions for this drug and to consult a healthcare professional prior to new drug use (including over-the-counter and herbal drugs).
31
Prinivil™ Pharmacologic Category
Lisinopril ACE Inhibitor
32
Prinivil™ FDA Approved Indications/Uses
Lisinopril * Acute myocardial infarction * Heart failure; adjunct * Hypertension
33
Prinivil™ Adverse Effects
Lisinopril * Chest pain * Hypotension * Syncope * Dizziness * Headache * Cough
34
Prinivil™ Dosage Forms
Lisinopril * Tablet * 2.5mg * 5mg * 10mg * 20mg * 30mg * 40mg
35
Prinivil™ Patient Education
Lisinopril * This drug may cause nausea, vomiting, dizziness, headache, or angioedema of face, lips, throat, or intestines. * Instruct patient to report signs/symptoms of hypotension, or a persistent cough. * Advise patient against sudden discontinuation of drug.
36
Cozaar™ Pharmacologic Category
Losartan Angiotensin II Receptor Blocker
37
Cozaar™ FDA Approved Indications/Uses
Losartan * Cerebrovascular accident * In hypertensive patients with left ventricular hypertrophy, prophylaxis * Diabetic neuropathy * T2DM * History of hypertension * Hypertension
38
Cozaar™ Adverse Effects
Losartan * Backache * Dizziness * Cough * Nasal congestion * Upper respiratory infection
39
Cozaar™ Dosage Forms
Losartan * Tablet * 25mg * 50mg * 100mg
40
Cozaar™ Patient Education
Losartan * Warn female patient to avoid pregnancy and to report a pregnancy that occurs during therapy. * Side effects may include dizziness, upper respiratory infection, nasal congestion, and back pain. * Warn patient to avoid use of potassium supplements or potassium-containing salt substitutes unless they consult healthcare provider.
41
Lopressor™ Pharmacologic Category
Metoprolol tartrate Beta-Adrenergic Blocker
42
Lopressor™ FDA Approved Indications/Uses
Metoprolol tartrate * Acute myocardial infarction * Angina pectoris * Hypertension
43
Lopressor™ Adverse Effects
Metoprolol tartrate * Bradyarrhythmia * Hypotension * Dizziness
44
Lopressor™ Dosage Forms
Metoprolol tartrate * Tablet * 25mg * 37.5mg * 50mg * 75mg * 100mg * IV * 1mg/ml
45
Lopressor™ Patient Education
Metoprolol tartrate * Patient should avoid activities requiring coordination until drug effects are realized, as drug may cause dizziness. * This drug may cause diarrhea, depression, or fatigue. * Advise patient to report signs/symptoms of cardiac failure. This drug may precipitate or exacerbate cardiac failure in CHF patients. * Tell patient to report signs/symptoms of arrhythmias or hypotension. * Drug may mask symptoms of hypoglycemia. Advise diabetics to report difficulties with glycemic control. * Patient should take extended-release tablet with or immediately following meals. * Advise patient against sudden interruption or discontinuation of drug, as this may exacerbate angina or cause myocardial infarction. Sudden discontinuation by patients with thyrotoxicosis may precipitate thyroid storm. * Instruct patient to take a missed dose as soon as possible, but if next dose is in less than 4 h, skip the missed dose.
46
Aldactone™ Pharmacologic Category
Spironolactone Renal Competitive Aldosterone Antagonist
47
Aldactone™ FDA Approved Indications/Uses
Spironolactone * Cirrhosis of liver—edema * Edema—nephrotic syndrome * Heart failure * NYHA Class III or IV * Hyperaldosteronism * Hypertension; add-on therapy
48
Aldactone™ Adverse Effects
Spironolactone * Gynecomastia * Diarrhea * Nausea * Vomiting * Somnolence * Disorder of menstruation * Erectile dysfunction
49
Aldactone™ Dosage Forms
Spironolactone * Tablet * 25mg * 50mg * 100mg
50
Aldactone™ Patient Education
Spironolactone * Warn patient to report dehydration, hypotension, or symptoms of worsening renal function. * Counsel male patient to report gynecomastia. * Side effects may include diarrhea, nausea, vomiting, abdominal cramping, fever, leg cramps, lethargy, mental confusion, decreased libido, irregular menses, and rash. * Suspension: Tell patient to take drug consistently with respect to food, either before or after a meal. * Advise patient to avoid potassium supplements and foods containing high levels of potassium, including salt substitutes.