2. Cardiac Glycosides
⢠Example: digoxin (Lanoxin)
⢠Drug Effects on Cardiac Action
⢠Positive inotropic: drugs that increase the force of
contraction
⢠Negative inotropic: drugs that decrease the force of con-
traction
⢠Positive chronotropic: drugs that increase heart rate
⢠Negative chronotropic: drugs that decrease heart rate
⢠Positive dromotropic: drugs that increase the rate of
electrical conduction through the myocardium
⢠Negative dromotropic: drugs that decrease the rate of
electrical conduction through the myocardium
3. ⢠Mechanisms of Action
⢠Positive inotropic effect: increases the force of
myocardial contraction
⢠Negative chronotropic effect: decreases the
heart rate
⢠Negative dromotropic: decreases the rate of
electrical conduction through the
atrioventricular node
6. ⢠Nursing Process Elements
⢠Be familiar with clientâs baseline VS, electrolyte
levels, and general health
⢠Assess the following before administering
digoxin:
⢠âCheck serum digoxin, potassium, magnesium,
and calcium levels
⢠âTake apical pulse for one full minute noting
rate, rhythm, and quality.
⢠âAssess for toxicity
7. ⢠Withhold digoxin and notify physician if:
⢠âPulse rate <60
⢠âSigniďŹcant change in pulse rate or rhythm
⢠âS&S of digoxin toxicity
⢠âSerum potassium level is less than 4 mEq/l
⢠âSerum digoxin level > 2 ng/ml (therapeutic range =
⢠0.8â2 ng/ml)
⢠Monitor clientâs ďŹuid intake and urinary output
⢠Monitor clientâs weight, signs of edema, lung, and
heart sounds
8. ⢠Assessment Alert
⢠Take apical pulse for one minute prior to
administering digoxin. Withhold digoxin and
call physician if heart rate is less than 60 bpm.
9. ⢠Nursing Diagnoses
⢠Cardiac output: decreased
⢠Tissue perfusion: ineffective
⢠Knowledge deďŹcit related to medications and
disease
10. ⢠Client teaching for self-care
⢠Instruct how to count pulse
⢠Instruct to call physician if pulse < 60 or > 110
⢠Instruct to call physician if heart rhythm irregular
⢠Review S&S of toxicity and instruct to report
them to physician
⢠Weigh each day and report > 2 lb gain per day
⢠Take digoxin as prescribed at same time each day
12. Mechanisms of Action
⢠Varies depending on the antiarrhythmic class
used
⢠Decreases the automaticity of cardiac tissue
⢠Alters the rate of conduction of electrical
impulses
⢠Alters the refractory period
15. Monitoring Effects of Antiarrhythmics
⢠Nursing Process Elements
⢠Assess heart rate and rhythm and BP prior to
administration and throughout therapy
⢠Monitor ECG
⢠Monitor for adverse effects
17. Client teaching for self-care
⢠Instruct in how to obtain pulse rate, and to
report changes in rate and rhythm to
physician
⢠Instruct to take doses round the clock and
what to do regarding missed doses and over-
the-counter medications
⢠Advise regarding importance of follow-up
appointments with health care provider
22. Forms of Nitrate Vasodilators
⢠Sublingual tablet
⢠âPlace tablet under tongue to dissolve within 5
minutes
⢠Extended-release buccal tablet
⢠âPlace tablet between lip and gum or between cheek
and gum to dissolve over 3â5 hours
⢠Oral sustained-release tablet or capsule
⢠Translingual spray
⢠âDo not shake canister
⢠âSpray under tongue
⢠âDo not inhale spray
23. ďąTransdermal ointment:
⢠âUse dose-determining applicator supplied
with ointment
⢠âNurse should wear gloves
ďąTransdermal Unit (patch)
⢠âNurse should wear gloves
ďąParenteral (IV)
24. Monitoring Effects of Nitroglycerin
ďąNursing Process Elements
⢠Be familiar with clients baseline VS
⢠Obtain BP, heart rate prior to administering medication
⢠Check BP and heart rate after administration
(hypotension may occur)
⢠Assess chest pain using pain scale, and assess for
associated symptoms: dyspnea, shortness of breath,
jaw, arm, neck pain, nausea, and diaphoresis
⢠Assess for blurred vision, headache, and dry mouth
⢠Assess for topical reactions when using the ointment or
transdermal unit
26. Nursing Diagnoses
⢠Pain: acute
⢠Tissue perfusion: ineffective
⢠Knowledge deďŹcit related to medications and
disease
27. Client teaching for self-care
⢠Instruct that sublingual tablets may be taken
prophylactically 5â10 minutes prior to exercise or other
stimulus known to trigger angina.
⢠Remind them to keep record of number of angina attacks,
amount of medication taken, and precipitating factors.
⢠Instruct that contact with water (bathing, swimming) does
not affect transdermal unit.
⢠Inform that the sublingual form can be taken while trans-
dermal unit or ointment is in place.
⢠When chest pain occurs, take one nitroglycerine tablet as
prescribed; if chest discomfort is not relieved in 3 minutes,
call 911.
28. ⢠Remind to report blurred vision, dry mouth,
faintness, dizziness, ďŹushing, or increase in
frequency or severity of pain to physician.
⢠Explain to change positions slowly and avoid
prolonged standing (postural hypotension)
⢠Inform that SL tablets should be kept in their
original container and tablets need to be
replaced every 6 months to assure potency.
29. ⢠Advise to take medication as directed, avoid
alcohol, and not to take over-the-counter
medications without approval of physician.
⢠Encourage to keep follow-up appointments
with health care provider.
31. Diuretics
⢠Mechanisms of Action
ďąThiazide diuretics
⢠Example: hydrochlorothiazide (HCTZ)
⢠âInhibits sodium reabsorption in the distal
tubule, thereby increasing excretion of water
and sodium.
⢠âEnhances excretion of magnesium, chloride,
and potassium.
32. Loop diuretics
⢠Example: furosemide (Lasix)
⢠âInhibits the reabsorption of sodium and
chloride in the ascending loop of Henle
⢠âIncreases risk of hypokalemia
⢠âReduces the ability of the kidneys to
concentrate urine
⢠âMore potent than the thiazides in
promoting sodium and ďŹuid excretion
33. Potassium-sparing diuretics
⢠Example: spironolactone (Aldactone)
⢠âPromotes sodium and chloride excretion
without concomitant loss of potassium
⢠âInhibits the action of the hormone
aldosterone thereby causing diuresis
⢠âLowers BP by unknown mechanism
⢠âIncreases risk of hyperkalemia
36. Monitoring Effects of Diuretics
⢠Nursing Process Elements
⢠Be familiar with clientâs baseline VS
⢠Obtain BP and heart rate prior to administering
medication
⢠Check BP and heart rate before and after
administration
⢠Monitor for signs of hypokalemia
⢠Fatigue
⢠Muscle weakness and cramps
⢠Rapid irregular pulse
⢠Vomiting
37. ⢠Shortness of breath
⢠Monitor ďŹuid intake and urinary output
⢠In hospital, weigh client daily. Monitor for:
⢠âedema
⢠âabnormal lung sounds
⢠âextra heart sounds
⢠Assess for postural hypotension
⢠Monitor serum levels
⢠âPotassium
⢠âSodium
⢠âChloride
⢠Blood urea nitrogen (BUN)
⢠Assess for digoxin toxicity if dehydration or hypokalemia
exists
38. Assessment Alert
⢠Take BP prior to and after administering
diuretics. Always monitor electrolytes prior to
administering diuretics.
39. Nursing Diagnoses
⢠Fluid volume: excess
⢠Knowledge deďŹcit related to medications,
disease, and nutrition
40. Client/family teaching
⢠Instruct regarding weighing at least once per
week
⢠Remind to have BP monitored weekly
⢠Advise to follow dietary guidelines, especially
regarding potassium and sodium
⢠Encourage to change positions slowly to avoid
a decrease in BP (postural hypotension)
41. ⢠Instruct to notify health care provider if
experiencing muscle weakness or cramping,
fatigue, or dizziness
⢠Advise to take medication as directed and to
not take over- the-counter drugs unless
approved by physician
⢠Encourage to keep follow-up appointments
with health care provider
43. Think Smart / Test Smart
⢠The generic names for the beta-blockers end
in âlol,â therefore, you will be able to identify
the beta- blockers from a list of drugs.
44. Mechanisms of Action
⢠Reduction in heart rate
⢠Reduces force of cardiac contraction
⢠Slows electrical conduction
⢠Reduces myocardial irritability
45. ⢠Management of cardiac arrhythmias
⢠Hypertension
⢠Tachyarrhythmias associated with digitalis
toxicity
⢠Angina Pectoris
46. Common Adverse Effects
⢠Weakness: fatigue
⢠Impotence
⢠Concerns for use: Precautions
⢠âIt may cause bronchoconstriction; therefore, its
use may be contraindicated in clients with chronic
pulmonary diseases
⢠âIt may promote congestive heart failure
therefore use cautiously in clients with risk for
heart failure.
47. Monitoring Effects of Beta-Adrenergic
Blocking Agents
⢠Nursing Process Elements
⢠Assess heart rate and rhythm, BP prior to
administration and throughout therapy
⢠Assess location, intensity, and duration of
anginal pain and associated symptoms
⢠Monitor ECG
⢠Monitor for adverse effects
49. Nursing Diagnoses
⢠Cardiac output, decreased
⢠Pain: acute
⢠Tissue perfusion: ineffective
⢠Knowledge deďŹcit related to medication and
disease
50. Client teaching for self-care
⢠Instruct in how to obtain pulse rate, and to report
changes in rate and rhythm to physician
⢠Instruct to take doses round the clock and what
to do regarding missed doses and over-the-
counter medications
⢠Advise to report chest pain to health care
provider immediately
⢠Advise regarding importance of follow-up
appointments with health care provider
51. CALCIUM CHANNEL ANTAGONISTS
⢠Example: nifedipine (Procardia)
ďąMechanisms of Action
⢠Relaxation of vascular smooth muscle and lowered BP
⢠Prevents or reverses spasms of coronary blood vessels
⢠Dilates coronary arteries and arterioles resulting in an
antianginal effect
⢠Reduces myocardial oxygen consumption
⢠Slows electrical impulse conduction (supraventricular
tachycardia)
52. Common Uses
⢠Prevention and treatment of angina pectoris
⢠Hypertension
ďąCommon Adverse Effects
⢠Hypotension
⢠Peripheral edema
⢠Dizziness
⢠Headache
53. Monitoring Effects of Calcium
Channel Antagonists Agents
⢠Nursing Process Elements
⢠Assess heart rate and rhythm, BP prior to
administration and throughout therapy
⢠Assess location, intensity, and duration of
anginal pain
⢠Monitor ECG
⢠Monitor for adverse effects
54. Assessment Alert
⢠Always take the clientâs BP and heart rate
before and after administering calcium
channel antagonists.
56. Think Smart / Test Smart
⢠The generic names of the ACE inhibitors end in
âpril,â therefore, you will be able to identify
them from a list.
57. Mechanism of Action
⢠Dilates peripheral arterioles
⢠Relaxes vascular smooth muscles
⢠Reduces peripheral resistance
⢠Interferes with conversion of angiotensin I to
angiotensin II
⢠Dilates peripheral vessels thereby reducing BP
60. Monitoring Effects of ACE Inhibitors
⢠Nursing Process Elements
⢠Be familiar with clientâs baseline VS
⢠Obtain BP and pulse rate prior to administering
medication
⢠Check BP and pulse rate after administration
⢠Monitor weight, edema, lung, heart sounds, and
I&O
⢠Assess for postural hypotension
⢠Encourage client to rise slowly from lying to
sitting position
61. Assessment Alert
⢠Always take the clientâs BP and heart rate prior
to and after administering ACE inhibitors.
63. Client teaching for self-care
⢠Instruct on monitoring BP weekly
⢠Remind to change positions slowly to prevent
rapid decrease in BP
⢠Encourage to follow dietary restrictions: low
sodium
⢠Instruct regarding reporting weight changes,
edema, and dizziness to physician
⢠Emphasize importance of follow-up
appointments with health care provider
64. ANTIMICROBIAL AGENTS
⢠ClassiďŹcation of Antimicrobial Agents
⢠Bactericidal and bacteriostatic
⢠âBactericidal agents have a killing action on
the bacteria
⢠âBacteriostatic agents inhibit the growth of
bacteria permitting the hostâs immunological
defenses to destroy the organism
65. Site of Action
⢠Agents that inhibit cell wall synthesis
⢠Agents that inhibit protein synthesis
⢠Agents that interfere with the permeability of
the bacterial cell membrane
⢠Agents with antimetabolite action block or
alter steps essential for the normal growth of
the bacteria
66. Narrow or Broad Spectrum of Action
⢠Narrow spectrum
⢠âEffective against a limited number of
organisms
⢠âUse when identity of organism and
susceptibility of the antibiotic is known
⢠âUsually do not disrupt normal bacterial ďŹora
67. ⢠Broad spectrum
⢠âAct on a wide variety of organisms
⢠âUseful in treating infections when the
identity and susceptibility to antimicrobial
treatment of the infecting organism is
unknown
⢠âHowever, they destroy the bodyâs normal
microbes and may permit superinfection and
diarrhea
69. ⢠Organ toxicity
⢠âHigh doses and/or over long periods of time
⢠âCan involve liver, kidneys, central nervous
system, etc
⢠Ototoxicity (detrimental effect on eighth nerve or
organs of hearing)
⢠Hematological disorders
⢠âAnemia
⢠âIncreased bleeding time
70. Major Classes
⢠Penicillins (beta-lactams) Example: ampicillin
(Polycillin)
⢠âBactericidal agents
⢠âInhibit the synthesis of the bacterial cell
wall
⢠âNarrow and broad-spectrum agents
71. Cephalosporins
⢠âChemically and pharmacologically related to
the penicillins
⢠âBactericidal or bacteriostatic effect
⢠âInterferes with bacterial cell wall syntheses
⢠âFour âgenerationsâ of cephalosporins
⢠âUse caution when client has allergy to
penicillins
72. Tetracyclines:
⢠Example: tetracycline (Tetracyn)
⢠âBacteriostatic
⢠âBroad-spectrum agents
⢠âInhibits protein synthesis in the bacterial cell
⢠âMay interfere with normal calciďŹcation of
temporary and permanent teeth and discolor
developing teeth
⢠âMay interfere with bone growth
⢠âClients more susceptible to sunburn
73. Macrolides:
⢠Example: erythromycin (Ery-Tab)
⢠âBacteriostatic
⢠âMay be bactericidal in high concentrations
⢠âInhibits protein synthesis in the bacterial
cell
74. Aminoglycosides:
⢠Example: gentamicin (Garamycin)
⢠âBactericidal or bacteriostatic
⢠âInhibits protein synthesis in the bacterial
cell
⢠âMay produce nephrotoxicity and ototoxicity
75. Monitoring Effects of Antibiotics
⢠Take a careful medication history before
administering antibiotics
⢠Know exactly why your client is receiving
antibiotics
⢠If ordered, obtain specimen for culture and
susceptibility before administering the antibiotic
⢠Know what a therapeutic response to antibiotic
treatment would include for each speciďŹc client
situation
⢠Administer oral doses of antibiotics on empty
stomach or with food as speciďŹed
76. ⢠Be aware of foodâdrug and drugâdrug
interactions, for example, penicillin can
interfere with effectiveness of oral
contraceptives.
⢠Monitor VS and S&S of infection
⢠Monitor WBC count, BUN, creatinine, and
other laboratory values
⢠Observe for adverse effects
⢠Observe for S&S of superinfections
77. Nursing Intervention Alert
⢠If cultures are ordered by the physician,
always obtain the specimen prior to
administering the ďŹrst dose of antibiotic.
79. Client teaching for self-care
⢠Advise to call health care provider if symptoms do
not improve
⢠Remind to take all doses of the medication even if
their symptoms are no longer present, and to
follow instructions regarding taking medication
with or without food
⢠Instruct to inform health care provider if
diarrhea, vomiting occur, black, hairy growth
develops on tongue, and vaginal irritation occurs
⢠Advise to keep all follow-up appointments with
health care provider
80. ANTICOAGULANTS
⢠Mechanism of Action
⢠Parenteral anticoagulants
⢠Example: heparin; enoxaparin (Lovenox)
⢠Exerts direct effect on blood coagulation
(clotting) by blocking the conversion of
prothrombin to thrombin and ďŹbrinogen to
ďŹbrin.
⢠Inhibits formation of new clots
81. Oral anticoagulant
⢠Example: warfarin sodium (Coumadin)
⢠Indirectly interferes with blood clotting by
depressing hepatic synthesis of vitamin K.
⢠Deters further extension of existing thrombi
and prevents new clots from forming.
⢠Has no effect on platelets.
⢠Unlike heparin, action is cumulative and more
prolonged.
82. Common Uses
⢠Heparin and Lovenox
⢠âProphylaxis and treatment of venous
thrombosis and pulmonary embolism (blood
clot to leg or lung)
⢠âPrevent thromboembolic complications
arising from cardiac surgery and vascular
surgery
⢠âDuring acute stages of myocardial infarction
(heart attack)
83. ⢠Coumadin
⢠Prophylaxis and treatment of deep venous
thrombosis and pulmonary embolism (blood clot
in leg or lung)
⢠Treatment of atrial ďŹbrillation.
⢠An adjunct in treatment of coronary occlusion,
cerebral transient ischemic attacks
⢠Prophylactic treatment for clients with prosthetic
cardiac valves
84. Common Adverse Effects
⢠Bleeding
⢠Hematuria
⢠Tarry stools
⢠Excessive vaginal bleeding
⢠Abdominal, ďŹank, or joint pain
⢠Headaches
⢠Changes in neurological status, restlessness
⢠Hematoma or bruising
⢠Vomiting blood
⢠Bleeding from the nose or gums
⢠Weak, rapid pulse rate
⢠Hypotension
85. Monitoring Effects of Heparin
⢠Nursing Process Elements
⢠Before administration check coagulation tests, hemoglobin,
hematocrit, and platelet counts.
⢠In general, the goal is to keep the partial thromboplastin
time (PTT) at 1.5â2.5 times its normal value of 35â45
seconds.
⢠Safely administer heparin via ordered route, i.e.,
subcutaneous injection, continuous intravenous infusion, or
intermittent intravenous infusion.
⢠No intramuscular injections
⢠Observe for S&S of bleeding
⢠Use soft toothbrush and electric razor
87. Monitoring Effects of Coumadin
⢠Before administration check coagulation tests, hemoglobin,
hematocrit, and platelet counts
⢠In general, the goal is to maintain a prothrombin time (PT)
of 1.5â2 times the control or reference value and maintain
the international normalized ratio (INR) at a value of 2â3.
The PT control value is generally 11â15 seconds
⢠The daily oral dose is based on the PT and INR results until
maintenance dosage is established
⢠Observe for S&S of bleeding
⢠No intramuscular injections
⢠No aspirin containing products
⢠Use soft toothbrush and electric razor
92. ⢠Mechanisms of Action
⢠Sulfonylureas
⢠Example: glyburide: (DiaBeta )
⢠Directly stimulates functioning pancreatic beta
cells to secrete insulin
⢠Increases sensitivity of peripheral insulin
receptors resulting in increased insulin binding
93. ⢠Biguanide
⢠Example: metformin (Glucophage)
⢠Increases glucose transport across cell
membrane, with enhanced glucose utilization
in skeletal muscles
⢠Increases the binding of insulin to its receptor
and potentiating insulin action
102. Monitoring Effects of Hypoglycemic
Agents
⢠Nursing Process Elements
⢠Monitor for S&S of hypoglycemia
⢠âFatigue, restlessness
⢠âCool, moist skin
⢠âWeakness and dizziness
⢠âHeadache
⢠âConfusion, slurred speech
⢠Monitor for S&S of hyperglycemia
⢠âFlushed, dry skin
⢠âIncreased urine output
⢠âIncreased thirst
⢠âIncreased appetite
⢠âDrowsiness
⢠Monitor blood glucose results as ordered
103. Assessment Alert
⢠Assess the lower extremities and feet of
clients with diabetes. Provide foot care and
assure that client has shoes to wear while in
the hospital.
109. Monitoring Effects of Bronchodilators
⢠Be familiar with clientâs baseline VS
⢠Monitor clientâs lung sounds, respiratory effort, and
oxygen saturation percentages via pulse oximetry
⢠Monitor for cyanosis of lips, ear lobes, mucous mem-
branes, and nailbeds
⢠Monitor theophylline plasma levels, if ordered.
Therapeutic range is 10â20 Âľg/ml.
⢠Observe client for adverse effects
⢠Ensure that client uses metered dose inhaler correctly
110. ⢠Nursing Diagnoses
⢠Ineffective Breathing pattern:
⢠Ineffective Airway clearance:
⢠Knowledge deďŹcit related to medications and
disease
112. Mechanisms of Action
⢠Laxatives
⢠Stimulant laxative:
⢠Example: bisacodyl (Dulcolax)
⢠Increases motility of gastrointestinal tract by chemical
irritation of the intestinal mucosa
⢠Increases the secretion of water into large and small intes-
tines
⢠Saline laxatives:
⢠Example: magnesium hydroxide (milk of magnesia)
⢠Draws water through the intestinal wall by osmotic action
increasing the ďŹuidity of the stool and stimulates greater
intestinal motility
113. ⢠Bulk-forming laxatives:
⢠Example: psyllium hydrophilic (Metamucil)
⢠Absorbs ďŹuid and the compound swells in the intestine,
stimulating peristaltic action.
⢠Lubricant laxatives:
⢠Example: mineral oil
⢠Act as lubricant to facilitate passage of fecal mass
through the intestines
⢠Stool softeners:
⢠Example: docusate sodium (Colace)
⢠Permits water and fat to penetrate and soften stool
114. ⢠Common Uses for Laxatives
⢠Prevent or treat constipation
⢠Prepare clients for a lower gastrointestinal X-ray
series or surgery
⢠Reduce the strain of defecation in clients with
cardiovascular disease or in postoperative clients
⢠Diagnose and treat parasitic infestations of the
gastrointestinal tract
⢠Help remove unabsorbed poisons from the
gastrointestinal tract
115. Histamine receptor antagonists
⢠Example: famotidine (Pepcid)
⢠Inhibits the action of histamine at the
histamine-sensitive H2 receptor site of the
parietal cells in the stomach
⢠Results in reduction in acid secretion
116. ⢠Proton pump inhibitors
⢠Example: lansoprazole (Prevacid)
⢠Suppresses gastric acid secretion by inhibiting
the gastric acid pump in the parietal cells of
the stomach
117. ⢠Common Uses for Histamine Receptor
Antagonists and Proton Pump Inhibitors
⢠Treatment of duodenal ulcer
⢠Treatment of gastric ulcer
⢠Gastroesophageal reďŹux disease
⢠Gastritis
⢠Erosive esophagitis
118. ⢠Adverse Effects of Histamine Receptor
Antagonists and Proton Pump Inhibitors
⢠Diarrhea
⢠Headache
120. ANALGESIC, ANTIPYRETIC, AND ANTI-
INFLAMMATORY AGENTS
⢠Mechanisms of Action
⢠Opioid analgesics
⢠Example: morphine (Roxanol)
⢠Opioid and opioid-like agents bind onto opioid
receptors found in the central nervous system
and act to inhibit the transmission of pain
impulses and alter pain perception
⢠Suppresses medullary cough centers
⢠Suppresses the motility of the gastrointestinal
tract
121. Assessment Alert
⢠Always assess clientâs respiratory rate prior to
and after administering morphine. Many
institutional policies state that the nurse
should not administer morphine to a client
with a respiratory rate of less than 10 breaths
per minute.
122. Salicylates
⢠Example: aspirin (Ecotrin)
⢠Anti-inďŹammatory action: Inhibits prostaglandin
synthesis
⢠Analgesic action: Acts peripherally to interfere with
action of prostaglandins
⢠Antipyretic action: In addition to inhibiting
prostaglandin synthesis, it lowers body temperature in
fever by causing centrally mediated peripheral
vasodilation and sweating
⢠Antiplatelet action: Aspirin inhibits platelet
aggregation, therefore, aspirin helps prevent strokes
and myocardial infarction (heart attack)
123. Nonnarcotic analgesic and antipyretic
⢠Example: acetaminophen (Tylenol)
⢠Produces analgesia by unknown mechanism,
perhaps by action on peripheral nervous
system
⢠Reduces fever by direct action on
hypothalamus, peripheral vasodilation, and
sweating
124. Nonsalicylates
⢠Example: celecoxib (Celebrex)
⢠Newer NSAIDs inhibit prostaglandin synthesis
by inhibiting COX-2
⢠Provides analgesic and anti-inďŹammatory
effects
⢠Less adverse effects on the gastrointestinal
system and less antiplatelet activity
125. Corticosteroids
⢠Example: prednisone (Pred-Pak)
⢠Synthetic steroid used primarily for its
glucocorticoid effectsâanti-inďŹammatory
agent
⢠Reduces the severity of inďŹammatory
symptoms
126. Opioid analgesics
⢠Moderate to severe pain
⢠Cough suppressant
⢠Suppressing the motility of the
gastrointestinal tract (diarrhea)
131. ⢠Cholinesterase Inhibitors
⢠Example: donepezil (Aricept)
⢠Mechanism of Action
⢠Enhances cholinergic function by increasing levels
of acetylcholine
⢠Common Uses
⢠Mild to moderate dementia associated with
Alzheimerâs disease
143. ANTIDEPRESSANTS
⢠There are two major classes: tricyclic
antidepressants and selective serotonin
reuptake inhibitors (SSRIs)
⢠Examples: nortriptyline (Aventyl), paroxetine
(Paxil)
144. ⢠Mechanisms of Action
⢠Tricyclic antidepressants
⢠Potentiates the effect of norepinephrine and
serotonin
⢠Possesses anticholinergic action
145. ⢠Selective serotonin reuptake inhibitors
⢠Inhibits uptake of serotonin in the CNS
⢠Common Uses
⢠Treatment of depression
146. ⢠Common Adverse Effects
⢠Fatigue
⢠Drowsiness
⢠Blurred vision and dry eyes
⢠Dry mouth and constipation
⢠Hypotension
148. ⢠Example: promethazine (Phenergan)
⢠Mechanisms of Action
⢠Inhibits the chemoreceptor trigger zone in the
medulla
⢠Common Uses
⢠Treatment and prevention of N&V
⢠Allergic conditions
⢠Motion sickness
⢠Sedation
149. ⢠Common Adverse Effects
⢠Sedation
⢠Disorientation
⢠Monitoring Effects of Antiemetic Agents
⢠Nursing Process Elements
⢠Assess for N&V, and abdominal pain
⢠Assess for ďŹuid volume deďŹcit (dry mucous
membranes, poor skin turgor, decreased urine output,
and thirst)
⢠Monitor I&O
⢠Implement safety precautions to prevent falls
150. ANTIFUNGUAL AGENTS
⢠Example: ďŹuconazole (DiďŹucan)
⢠Mechanisms of Action
⢠Inhibits synthesis of fungal sterols
⢠Affects the permeability of the fungal cell
membrane or protein synthesis within the cell
⢠Common Uses
⢠Treatment of fungal infections
⢠Prevention of fungal infections
⢠Common Adverse Effects
⢠abdominal discomfort
151. ANTIHISTAMINE AGENTS
⢠Example: fexofenadine (Allegra)
⢠Mechanisms of Action
⢠Blocks the effects of histamine at peripheral
histamine-1 receptors
⢠Common Uses
⢠Relief of allergic rhinitis
⢠Urticaria
⢠Common Adverse Effects
⢠No common adverse effects
152. Nursing Intervention Alert
⢠Apple, orange, and grapefruit juice will
decrease the absorption of fexofenadine
(Allegra).
153. ANTIPLATELET AGENTS
⢠Mechanisms of Action
⢠Glycoprotein IIb/IIIa inhibitors: eptiďŹbatide (Integrilin)
⢠Platelet Aggregation Inhibitors: dipyridamole (Persantine)
⢠Platelet Adhesion Inhibitors: clopidogrel (Plavix)
⢠Common Uses
⢠Prevention of myocardial infarction or stroke
⢠Treatment of acute coronary syndromes
⢠Common Adverse Effects
⢠Dizziness
⢠Headache
⢠Bruising
154. ⢠Client teaching for self-care
⢠Instruct to take medication as prescribed and to avoid
using over-the-counter medication containing aspirin
or NSAIDs without prior approval from physician
⢠Advise to avoid using alcohol and tobacco products due
to the vasoconstriction action
⢠Instruct to notify physician if signs of bleeding
(bruising, headache, blood in urine, dark stools,
headache, weakness)
⢠Encourage to keep appointments with health care
providers
155. ANTIVIRAL AGENTS
⢠Example: acyclovir (Zovirax)
⢠Mechanisms of Action
⢠Inhibits viral DNA replication
⢠Common Uses
⢠Treatment of herpes zoster (shingles)
⢠Treatment of herpes simplex virus types 1 and 2
⢠Treatment of genital herpes infections
⢠Common Adverse Effects
⢠Headache and dizziness
⢠Nausea, vomiting, and diarrhea
157. ⢠Mechanisms of Action
⢠Reduces total cholesterol, LDL, and triglycerides
and increases HDL
⢠Common Uses
⢠Reduce lipids/cholesterol in order to decrease
risk for myocardial infarction and stroke
⢠Common Adverse Effects
⢠Indigestion, diarrhea, and constipation
⢠Rash