Exam 3 (Drugs 101 - 150) Flashcards

1
Q

Insulin Aspart

A

Novolog

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2
Q

Insulin is the primary hormone responsible for carrying out proper glucose utilization in metabolic processes

A

Insulin Aspart, Insulin Lispro, Insulin Detemir

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3
Q

Hypoglycemic reactions are not uncommon in diabetics and may be caused by excessive insulin dose or when glucose absorption is decreased due to fasting, diarrhea, or vomiting

A

Insulin Aspart, Insulin Lispro, Insulin Detemir

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4
Q

May cause lipodystrophy at the injection site

A

Insulin Aspart, Insulin Lispro, Insulin Detemir

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5
Q

Administer 5 - 10 minutes before eating

A

Insulin Aspart

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6
Q

Estrogens (conjugated)

A

Premarin

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7
Q

A mixture of naturally occurring estrogens derived from pregnant mares’ urine

A

Premarin

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8
Q

CI in patients with known or suspected cancer of the breast except in selected patients being treated for metastatic disease. Do not use in patients with known or suspected estrogen-dependent neoplasia, known or suspected pregnancy, undiagnosed genital bleeding, or in pts with thrombophlebitis, thrombosis, or thromboembolic disorders

A

Premarin, Estradiol (topical)

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9
Q

Estrogens have been reported to increase the risk of endometrial carcinoma and to increase the risk of cardiovascular events including MI, stroke, pulmonary emboli, and DVT in postmenopausal women. Because of these risks, estrogens should be prescribed at the lowest effective dose and for the shortest duration consistent with treatment goals

A

Premarin

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10
Q

AE’s include rash, acne, alopecia, hirsutism, abnormal menstrual BLEEDING, edema, changes in weight, cholestatic JAUNDICE, changes in cervical erosion and cervical secretions, mental depression, pyrexia, insomnia, nausea, and somnolence

A

Premarin

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11
Q

Report any severe side effects to your physician including pains in the legs, coughing blood, abnormal vaginal bleeding, skin yellowing, and abdominal pain

A

Premarin

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12
Q

Read patient information sheet carefully

A

Premarin

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13
Q

Hydroxyzine Pamoate (antianxiety)

A

Vistaril

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14
Q

Antagonizes the H1 receptors in the subcortical region of the CNS. Primary skeletal muscle relaxation, bronchodilator activity, and antihistaminic and analgesic activity have been demonstrated

A

Hydroxyzine Pamoate

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15
Q

May potentiate the effects of opioids and barbiturates, dosage requirements may be necessary

A

Hydroxyzine Pamoate

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16
Q

Sedating drugs may cause confusion and over sedation in the elderly; elderly patients should be started on a lower dose

A

Hydroxyzine Pamoate

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17
Q

The most common AE’s are dry mouth and drowsiness. Drowsiness is usually transitory in nature and may disappear after a few days of treatment

A

Hydroxyzine Pamoate

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18
Q

Tizanidine HCl

A

Zanaflex

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19
Q

Agonist at alpha-2 adrenergic receptor sites and presumably reduces spasticity by increasing presynaptic inhibition of motor neurons. Does not affect skeletal muscle fibers or the neuromuscular junction with minimal effects on monosynaptic spinal reflexes

A

Tizanidine

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20
Q

Structurally similar to clonidine but with much lower effects on blood pressure

A

Tizanidine

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21
Q

Tablet and capsule formulations are bioequivalent when given in the fasted state, but not when given with food. When given with food, the plasma concentrations of the tablet form are increased and the plasma concentration of the capsule form are decreased

A

Tizanidine

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22
Q

Oral contraceptives decrease this drug’s clearance

A

Tizanidine

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23
Q

Occasional cases of liver injury have been reported during therapy. Monitor liver enzymes before and during treatment (baseline, 1, 3, 6 months) and stop therapy if liver function tests > 3x ULN. Animal studies have shown dose-related retinal degeneration & corneal opacities

A

Tizanidine

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24
Q

More frequent AE’s include dry mouth, drowsiness, asthenia, bradycardia, hypotension, and dizziness. Less frequent include constipation, ABNORMAL LIVER FUNCTION TESTS, BLURRED VISION, rhinitis, nervousness, vomiting, speech disorder, and pharyngitis

A

Tizanidine

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25
Q

Methylphenidate HCl

A

Ritalin (SR, LA), Methylin, Metadate

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26
Q

Presumably activates the brain stem arousal system and cortex to produce its stimulant effect

A

Methylphenidate

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27
Q

May produce hypertensive crisis when used with MAOI’s

A

Methylphenidate

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28
Q

CI in patients with anxiety, tension, or agitation, in patients with glaucoma or motor tics, and in patients with a family history or diagnosis of Tourette’s syndrome

A

Methylphenidate

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29
Q

Should not be used in children < 6 yo

A

Methylphenidate

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30
Q

Take last dose early in the evening to avoid insomnia. LA capsules may be swallowed whole or the contents sprinkled over soft food and ingested without chewing

A

Methylphenidate

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31
Q

Ciprofloxacin HCl

A

Cipro (XR)

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32
Q

A fluoroquinolone antibiotic which prevents the synthesis of bacterial DNA by interfering with the enzyme DNA gyrase. Has a wide range of activity against gram-negative and gram-positive bacteria.

A

Ciprofloxacin

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33
Q

Antacids and iron salts decrease bioavailability. Probenecid increases serum levels by decreasing exertion. NSAID’s may lower seizure thresholds and predispose patients to convulsive seizures when taking this drug.

A

Ciprofloxacin

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34
Q

Do not use in children, adolescents, or pregnant women due to permanent lesions in weight-bearing joints. Do not use in patients receiving theophylline. Patients should be well hydrated to avoid crystalluria.

A

Ciprofloxacin

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35
Q

Quinolones have been shown to cause ruptures of the shoulder, hand, and Achilles tendons.

A

Ciprofloxacin

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36
Q

Most common AE’s are nausea, RASH, diarrhea, sun sensitivity, and dizziness

A

Ciprofloxacin

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37
Q

Drink a full glass of water after each dose. May be taken without regards to meals, although it is preferable to take dose two hours following a meal. Do not take antacids during therapy.

A

Ciprofloxacin

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38
Q

Suspension may be stored at room temperature or in the refrigerator and is stable for 14 days after reconstitution. Shake vigorously for 15 seconds before each dose

A

Ciprofloxacin

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39
Q

Do not take antacids or products containing calcium, zinc, or iron at the same time as this drug. This drug can be taken 2 hours before or 6 hours after these products

A

Ciprofloxacin

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40
Q

Lansoprazole

A

Prevacid

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41
Q

Inhibits the H+/K+ ATPase enzyme system at the secretory surface of the gastric parietal cell. This enzyme system is involved in the movement and production of gastric acid.

A

Lansoprazole

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42
Q

Ezetimibe

A

Zetia

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43
Q

Lipid-lowering compound that selectively inhibits the intestinal absorption of cholesterol and is related to phytosterols. Appears to act at the brush border of the small intestine to inhibit cholesterol absorption thereby decreasing the delivery of cholesterol to the liver

A

Ezetimibe

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44
Q

AE’s include myalgia, increased CPK, elevations in liver transaminases, hepatitis, thrombocytopenia, urticaria, arthralgia, and myopathy/rhabdo

A

Ezetimibe

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45
Q

Do not take within 2 hours before or 4 hours after the administration of a bile acid sequestrant (cholestyramine)

A

Ezetimibe

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46
Q

Propranolol HCl

A

Inderal (LA), Innopran XL

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47
Q

Causes non-selective blockage of beta-adrenergic receptors resulting in 1) a decreased HR, 2) a decrease in systolic and diastolic BP, 3) an inhibition of isoproterenol tachycardia, and 4) a decrease of reflex tachycardia

A

Propranolol

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48
Q

Toxic effects may be increased with concurrent use of VERAPAMIL

A

Propranolol

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49
Q

CI in patients with cardiogenic shock, bronchial asthma, sinus bradycardia, greater than 1st degree heart block, and CHF, unless secondary to tachyarrhythmia treatable with propranolol

A

Propranolol

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50
Q

Patients with diabetes need to be aware that this agent can cause masking of hypoglycemic symptoms

A

Propranolol

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51
Q

Fentanyl (transdermal)

A

Duragesic

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52
Q

An opioid analgesic, therefore analgesia is produced centrally via action on the central opiate receptors. Interacts predominantly with the mu-opioid receptor.

A

Fentanyl

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53
Q

Patches should be applied to non-irritated and non-irradiated skin on a flat surface of the upper torso. Do not apply to extremities below the knee or elbow. Hair at the application site should be clipped (not shaved) prior to system application.

A

Fentanyl

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54
Q

Patches should be applied immediately upon removal from the sealed package. The transdermal system should be pressed firmly in place with the palm of the hand for 10 - 20 seconds. Each patch may be worn continuously for 72 hours.

A

Fentanyl

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55
Q

Used systems should be folded so that the adhesive side of the system adheres to itself and then flushed down the toilet immediately upon removal. Do not cut or puncture systems

A

Fentanyl

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56
Q

Nystatin (topical)

A

Nystop

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57
Q

An antimycotic polyene antibiotic obtained from Streptomyces noursei. MOA is that it binds to sterols in the cell membrane of susceptible Candida species, changing the permeability of the cell membrane. Fungicidal and fungistatic against many fungi. It is not absorbed from intact skin or mucous membranes

A

Nystatin

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58
Q

Cream, ointment, and powder preparations are not to be used in ophthalmic, intravaginal, oral or systemic infections

A

Nystatin

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59
Q

Do not use in or around the eyes - not for opthalmic use

A

Nystatin

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60
Q

Doxycycline Hyclate

A

Vibramycin & Vibra-Tabs

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61
Q

Tetracycline antibiotic which prevents bacterial protein synthesis by competitively binding to the 30S ribosomal subunit. Bacteriostatic at normal dosage ranges.

A

Doxycycline

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62
Q

May impair the action of bactericidal antibiotics. May impair the systemic absorption of oral contraceptives. Absorption may be impaired by aluminum, bismuth, calcium, magnesium, zinc, iron salts, and urinary alkalinizers

A

Doxycycline

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63
Q

Use with precaution in children < 8 yo (during tooth development). Cases of C. diff associated diarrhea have occurred during treatment

A

Doxycycline

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64
Q

Preferably taken on an empty stomach - one hour before or two hours after meals - with a full glass of water. Taken at intervals, preferably around the clock. Avoid prolonged exposure to the sunlight.

A

Doxycycline

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65
Q

Insulin Lispro

A

Humalog

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66
Q

Administer 15 minutes before eating

A

Insulin Lispro

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67
Q

Carbidopa with Levodopa

A

Sinemet (CR)

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68
Q

Levodopa crosses the BBB and is converted into dopamine in the basal ganglia. A large portion of levodopa is converted to dopamine in extracerebral tissue. Dopamine does not cross the BBB. Carbidopa inhibits the dopa-decarboxylase in extracerebral tissue, thereby increasing the levels of levodopa available to the CNS and decreases the side effects (nausea) seen from high levels of peripheral dopamine.

A

Carbidopa with levodopa

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69
Q

Hydantoins and pyridoxine (vitamin B6) may decrease effectiveness. Hypertensive crisis may occur if given with MAOI’s.

A

Carbidopa with levodopa

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70
Q

CI in patients with narrow-angle glaucoma, in patients with a suspicious, undiagnosed skin lesion or a history of melanomas, and in patients currently taking MAOI’s

A

Carbidopa with levodopa

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71
Q

D/C levodopa therapy at least 8 hours before initiation of Sinemet therapy

A

Carbidopa with levodopa

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72
Q

AE’s include DYSTONIC or involuntary movements, depression, dementia, and nausea

A

Carbidopa with levodopa

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73
Q

_____ CR may be given whole or in half tablets but should not be crushed or chewed

A

Carbidopa with levodopa

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74
Q

Avoid vitamin B6 (pyridoxine) products

A

Carbidopa with levodopa

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75
Q

Valsartan

A

Diovan

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76
Q

Blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor found in many tissues (ARB)

A

Valsartan

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77
Q

NSAID’s, including COX-2 inhibitors, may decrease effects and increase risk of renal function deterioration

A

Valsartan

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78
Q

Use with caution in volume or salt-depleted patients due to excessive hypotension

A

Valsartan

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79
Q

Famotidine

A

Pepcid

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80
Q

Competitively inhibits histamine at the H2 receptors, including receptors on gastric cells. Inhibits basal, nocturnal, and food stimulated gastric secretion.

A

Famotidine

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81
Q

Shake suspension well and discard unused portion after 30 days

A

Famotidine

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82
Q

Antacids may be given concomitantly to relieve acute pain

A

Famotidine

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83
Q

Sitagliptin Phosphate

A

Januvia

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84
Q

Inhibits the dipeptidyl-peptidase-4 (DPP-4) enzyme - this enzyme is responsible for deactivating the incretin hormones glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)

A

Sitagliptin

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85
Q

The use of this drug with drugs that may cause hypoglycemic reactions (including sulfonylureas & insulin) has not been adequately studied and these combinations should be avoided.

A

Sitagliptin

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86
Q

Most common AE is nasopharyngitis (5%)

A

Sitagliptin

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87
Q

May be taken without regard to meals. Quarterly HbA1c testing should be performed

A

Sitagliptin

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88
Q

Eszopiclone

A

Lunesta

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89
Q

A pyrrolopyrazine of the cyclopyrrolone class (structurally unrelated to benzodiazepines). Thought to act at GABA-receptor complexes at binding sites located near or coupled to BZD receptors

A

Eszopiclone

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90
Q

Additive CNS depressant effect is seen when this drug is given with CNS depressants, including alcohol.

A

Eszopiclone

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91
Q

Sleep disturbances may be a sign of a physical and/or psychiatric disorder. The failure of insomnia to remit after 10 days of treatment may indicate the presence of a primary physical and/or psychiatric illness.

A

Eszopiclone

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92
Q

Most common AE’s (>10%) are drowsiness, HA, and an unpleasant taste sensation. Less common AE’s (< 5%) include dry mouth, anxiety, depression, dysmenorrhea, gynecomastia, and infection

A

Eszopiclone

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93
Q

Preferably taken on an empty stomach. High fat meals delay onset of action. Take immediately before bedtime. A rapid decrease or abrupt D/C of therapy may precipitate withdrawal symptoms

A

Eszopiclone

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94
Q

Temazepam

A

Restoril

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95
Q

Facilitates the inhibitory neurotransmitter action of GABA, which mediates both pre- and post-synaptic inhibition in all regions of the CNS

A

Temazepam

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96
Q

Insomnia may be a sign of an underlying psychiatric disorder. Reevaluate therapy if insomnia fails to remit after 10 days of treatment

A

Temazepam

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97
Q

This medication is not intended to be used for longer than 10 consecutive days

A

Temazepam

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98
Q

Verapamil HCl

A

Isoptin, Calan, Verelen

99
Q

Calcium-channel blocker which inhibits the movement (influx) of calcium ions across specific cellular membranes (slow channels) resulting in 1) dilation of coronary arteries and arterioles resulting in a decreased vascular resistance, 2) coronary spasm inhibition, 3) lowering of arterial BP, 4) slowing of SA and AV conduction, and 5) prolongation of AV node ERP & FRP

A

Verapamil

100
Q

Therapeutic and toxic effects of BETA-BLOCKERS and prazosin may be increased when used with this drug.

A

Verapamil

101
Q

CI in patients with severe left ventricular dysfunction hypotension, cardiogenic shock, sick sinus syndrome, and 2nd or 3rd degree AV block

A

Verapamil

102
Q

AE’s include hypotension, peripheral edema, dizziness, HA, constipation, and nausea

A

Verapamil

103
Q

Take each dose on an empty stomach at least one hour before or two hours after a meal. Do not D/C therapy without first consulting a physician

A

Verapamil

104
Q

Chlorpheniramine with Hydrocodone

A

Tussionex

105
Q

A narcotic which depresses the cough reflex center in the medulla oblongata & an H1 antihistamine receptor antagonist which possesses anticholinergic activity

A

Chlorpheniramine with Hydrocodone

106
Q

Use with extra caution postoperatively and in patients with pulmonary disease, obstructive bowel disease, increased intracranial pressure, or head injury

A

Chlorpheniramine with Hydrocodone

107
Q

Enalapril Maleate

A

Vasotec

108
Q

Undergoes hydrolysis after absorption to form the active metabolite enalaprilat

A

Enalapril

109
Q

Competitively inhibits angiotensin-converting enzyme (ACEI)

A

Enalapril

110
Q

Capsaicin may increase the incidence of coughing. Diuretics (especially potassium-sparing diuretics) and potassium supplements may increase hyperkalemia

A

Enalapril

111
Q

Avoid nonprescription cough, cold, and allergy medications unless otherwise directed

A

Enalapril

112
Q

Solifenacin Succinate

A

Vesicare

113
Q

A competitive muscarinic receptor antagonist

A

Solifenacin

114
Q

CI in patients with urinary retention, gastric retention, or uncontrolled narrow-angle glaucoma and in patients who are at risk for these conditions

A

Solifenacin

115
Q

AE’s are usually mild and transient and include (in order of occurrence): dry mouth, constipation, blurred vision, UTI, dyspepsia, nausea, abdominal pain, dizziness, fatigue, and dry eyes

A

Solifenacin

116
Q

Avoid prolonged exposure to hot weather

A

Solifenacin

117
Q

Estradiol (topical)

A

Vivelle-Dot

118
Q

Estrogens promote growth and development of the vagina, uterus, and fallopian tubes, and enlargement of the breasts. They are also involved in the process of menstruation. Estradiol is the more potent of the estrogens with estrone and estriol being less potent. Transdermal applied estradiol avoids the first-pass metabolism of orally administered estradiol to estrone

A

Estradiol (topical)

119
Q

Irritation of application site, EDEMA, THROMBOEMBOLIC disorders, breast tenderness, disturbances in menstruation, and depression

A

Estradiol (topical)

120
Q

Discuss the uses and dangers of estrogen therapy (package insert)

A

Estradiol (topical)

121
Q

Closely follow the cyclic administration. Water will not affect system. Do not use scissors to remove protective pouch. Avoid application sites that are oily, damaged, irritated, or wet. Do not apply to the waistline, since tight clothing may rub system off.

A

Estradiol (topical)

122
Q

Pramipexole Dihydrochloride (antiparkinson agent)

A

Mirapex

123
Q

A nonergot dopamine receptor agonist with a higher affinity to D3 dopamine receptors than D2 or D1 receptors. Principle site of action for the treatment of Parkinson’s disease appears to be in the striatum and substantial nigra

A

Pramipexole

124
Q

Orthostatic hypotension is common during dose escalations. Careful dose titrations minimize the clinical effect of the orthostatic hypotension. May potentiate the dopaminergic side effects (dyskinesia) of levodopa therefore requiring a lowering of the levodopa dose. Some patients have reported suddenly falling asleep during activities of daily living, even after one year therapy

A

Pramipexole

125
Q

AE’s found in early Parkinson’s disease include dizziness (25%), somnolence (22%), asthenia (14%), etc. AE’s found in advanced Parkinson’s disease include orthostatic hypotension (53%), dyskinesia (47%), insomnia (27%), dizziness (26%), etc.

A

Pramipexole

126
Q

Patients should be informed that hallucinations may occur during therapy. Report any changes in vision. Report any new or increased intense urges (gambling, sexual, other). May cause orthostatic hypotension.

A

Pramipexole

127
Q

Carbamazepine

A

Tegretol (XR), Carbatrol ER, Equetrol ER

128
Q

Appears to act by reducing polysynaptic responses and blocking the post-tetanic potentiation.

A

Carbamazepine

129
Q

CI in patients hypersensitive to tricyclic compounds and in patients with bone marrow suppression. Patients of Asian descent should be tested for HLA-B*1502 bc these patients have a much higher risk of developing serious skin reactions including Stevens-Johnson syndrome and toxic epidermal necrolysis

A

Carbamazepine

130
Q

Rare reports of aplastic anemia, agranulocytosis, and Stevens-Johnson syndrome have been reported. Contact a physician immediately if fever, sore throat, mouth ulcers, bruising, or skin rash occurs.

A

Carbamazepine

131
Q

Taken with food or milk. Drink a full glass of water following administration of chewable tablets

A

Carbamazepine

132
Q

Phenytoin Sodium (extended)

A

Dilantin Kapseals

133
Q

Increases the extrusion of sodium ions from neurons and cardiac myocytes. This produces a stabilization of the excitable membrane to repetitive stimuli. The primary site of action appears to be the motor cortex

A

Phenytoin

134
Q

MANY drug interactions. D/C use if rash develops

A

Phenytoin

135
Q

AE’s include nystagmus, ATAXIA, SLURRED SPEECH, MENTAL CONFUSION, N/V, RASH, hirsutism, gingival hyperplasia, constipation, dizziness, drowsiness

A

Phenytoin

136
Q

Take with food to enhance absorption and to reduce GI upset. Practice good oral hygiene to help prevent gingival hyperplasia. Diabetic patients should monitor blood glucose levels closely. Do not D/C therapy without first consulting a physician.

A

Phenytoin

137
Q

Levalbuterol HCl

A

Xopenex

138
Q

A sympathomimetic which stimulates adenyl cyclase, the enzyme which catalyzes the formation of cAMP from ATP. This formation causes relaxation of bronchial, uterine, and vascular smooth muscle through stimulation of beta-2 adrenergic receptors

A

Levalbuterol

139
Q

Solution for inhalation can produce paradoxical bronchospasm, which can be life-threatening

A

Levalbuterol

140
Q

AE’s listed in approximate order of frequency: dizziness, pharyngitis, and rhinitis

A

Levalbuterol

141
Q

Do not take more frequently than recommended. Vials are distributed in foil pouches in groups of 12. Once a foil pouch is opened, the vials inside should be used within 2 weeks. After opening the foil, keep the vials inside the pouch until ready to use. Solution in the vial should be colorless.

A

Levalbuterol

142
Q

Shake canister well before each inhalation. Prime with 4 sprays before first use and if not used for 3 days. Clean mouthpiece at least once a week by removing the canister, running warm water through it for 30 seconds, and letting it air dry thoroughly.

A

Levalbuterol

143
Q

Cephalexin Monohydrate

A

Keflex

144
Q

A first generation cephalosporin which inhibits bacterial cell wall synthesis via acylation of the transpeptidase enzyme.

A

Cephalexin

145
Q

CI in patients hypersensitive to PCNs/cephalosporins. Estimated incidence of cross-sensitivity is 5 - 16%. Cases of pseudomembranous colitis have occurred during treatment.

A

Cephalexin

146
Q

AE’s include N/V, DIARRHEA, HIVES, ITCHING, and RASH

A

Cephalexin

147
Q

Preferably taken on an empty stomach (one hour before or two hours after meals) with a full glass of water. Take at even intervals, preferably around the clock. Keep suspension refrigerated

A

Cephalexin

148
Q

Desvenlafaxine

A

Pristiq

149
Q

A potent inhibitor of neuronal serotonin and norepinephrine reuptake

A

Desvenlafaxine

150
Q

ANTIDEPRESSANTS INCREASE SUICIDAL THOUGHTS AND ACTIONS IN SOME CHILDREN, ADOLESCENTS, AND YOUNG ADULTS. Should not be used within 14 days of D/C MAOI therapy. Wait at least one week after stopping this drug to initiate an MAOI

A

Desvenlafaxine

151
Q

Use cautiously in patients with a history of seizures. Not indicated for use in pediatric patients.

A

Desvenlafaxine

152
Q

Most common AE’s include nausea, dry mouth, anorexia, constipation, drowsiness, insomnia, dizziness, sweating, erectile dysfunction, and decreased libido

A

Desvenlafaxine

153
Q

Continued therapy of up to 2 weeks may be needed to show noticeable improvement

A

Desvenlafaxine

154
Q

Do not abruptly stop therapy before consulting a physician. Matrix tablet shell may be found intact in the stool.

A

Desvenlafaxine

155
Q

Mometasone Furoate Monohydrate (intranasal)

A

Nasonex

156
Q

Adrenocorticoid that binds to certain receptor proteins found in the cytoplasm of sensitive cells to form a steroid-receptor complex. The steroid-receptor complex enters the nucleus of the cell where it reacts with chromatin, or DNA. The steroid (or possibly the receptor) then uses stored information to stimulate or inhibit the transcription of mRNA.

A

Nasonex, Triamcinolone acetonide (topical), Fluticasone propionate (inhalation)

157
Q

Use with caution in patients with tuberculous infections of the respiratory tract, untreated fungal, bacterial, or systemic viral infections, ocular herpes simplex, or unhealed wounds of the nasal mucosa

A

Nasonex, Triamcinolone acetonide (except for nasal part)

158
Q

AE’s include HA (26%), viral infection (14%), pharyngitis (12%), epistaxis (11%), cough (7%), upper respiratory tract infection (6%), dysmenorrhea, muscle pain, and sinusitis (5%)

A

Nasonex

159
Q

Shake bottle well before each use. Therapeutic effects are not seen at once, benefits are usually seen in a few days but may take as long as three weeks. If no improvement is evident by that time, use should be D/C. Clear nasal passages of secretions prior to use. Oral decongestants may be used if needed.

A

Nasonex

160
Q

Ziprasidone HCl (antipsychotic)

A

Geodon

161
Q

Exact MOA unknown, but thought to act by antagonism of dopamine D2 and serotonin 5-HT2 receptors. Also has been shown to be an antagonist at histamine H1 and alpha-1-adrenergic receptors

A

Ziprasidone

162
Q

Should not be used with other drugs that prolong the QTc interval including dofetilide, sotalol, quinidine, other Class Ia and III antiarrhythmics, FQ’s, etc

A

Ziprasidone

163
Q

CI IN PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS. CI in patients with a known history of QT prolongation, with recent MI, with uncompensated HF, & in pts currently taking a drug which prolongs the QTc interval

A

Ziprasidone

164
Q

Rare cases of Neuroleptic Malignant Syndrome (NMS) have occurred in patients taking antipsychotic medications. Rare cases of leukopenia/neutropenia and agranulocytosis have been reported in patients taking antipsychotic agents

A

Ziprasidone

165
Q

Most common AE’s include: drowsiness, nausea, constipation, dyspepsia, dizziness, akathisia, cold symptoms, EPS, diarrhea, rhinitis, asthenia, dry mouth, dystonia, and non-allergic rash

A

Ziprasidone

166
Q

This drug can cause serious heart arrhythmias. Take with food to help its absorption. Do not D/C abruptly. May take several weeks to see symptom improvement. Use appropriate precautions against heat exposure and dehydration

A

Ziprasidone

167
Q

Niacin (ER)

A

Niaspan

168
Q

AKA nicotinic acid; functions in the body after conversion to nicotinamide adenine dinucleotide (NAD). Lowers cholesterol by a mechanism unrelated to its actions as a vitamin. Increases lipoprotein lipase activity, decreases lipolysis in adipose tissue, and decreases esterification of triglycerides in the liver

A

Niacin

169
Q

Bile acid sequestrants will decrease absorption; a minimum of 4 hours should elapse between administration of these drugs. Rare cases of rhabdomyolysis have occurred in patients taking niacin with HMG-CoA reductase inhibitors.

A

Niacin

170
Q

CI in patients with significant or unexplained hepatic dysfunction, active PUD, or arterial bleeding.

A

Niacin

171
Q

Most frequent AE’s include flushing (88%), pruritis (6%), and rash (5%)

A

Niacin

172
Q

Take at bedtime with a low-fat snack. Taking on an empty stomach is not recommended

A

Niacin

173
Q

Flushing is a common AE and usually subsides after a few weeks of therapy. Aspirin or NSAIDs taken shortly before bedtime may minimize flushing. Avoid alcohol around the same time as this drug to avoid flushing reactions

A

Niacin

174
Q

Fluconazole

A

Diflucan

175
Q

A highly selective inhibitor of fungal cytochrome P450 sterol C-14 alpha-demethylation. Mammalian cell demethylation is much less sensitive to fluconazole inhibition

A

Fluconazole

176
Q

No evidence of cross hypersensitivity between this drug and other azole antifungal agents

A

Fluconazole

177
Q

Nausea, HA, abdominal pain, diarrhea, dizziness, dyspepsia, and taste perversion are common AE’s

A

Fluconazole

178
Q

Gemfibrozil

A

Lopid

179
Q

Decreases serum triglycerides and VLDL-cholesterol and increases HDL-cholesterol. Reduction of triglycerides is due to an inhibition of peripheral lipolysis and reduction of hepatic extraction of free fatty acids.

A

Gemfibrozil

180
Q

Coadministration with LOVASTATIN may cause severe myopathy or rhabdomyolysis

A

Gemfibrozil

181
Q

CI in patients with hepatic or severe renal dysfunction and preexisting gallbladder disease. May cause cholelithiasis

A

Gemfibrozil

182
Q

AE’s include dyspepsia (19.6%), abdominal pain (9.8%), diarrhea (7.2%), nausea (2.5%), and fatigue (3.8%)

A

Gemfibrozil

183
Q

Lithium Carbonate

A

Lithonate, Lithotabs, Lithobid

184
Q

Exact MOA in the treatment of mania is unknown. Mood stabilizing effect may be due to an antagonism of the release of NE and dopamine from nerve terminals or from increasing the reuptake and inactivation of catecholamines. Does NOT inhibit the release of serotonin

A

Lithium carbonate

185
Q

CI in patients with significant renal or CV disease, severe debilitation, dehydration, or sodium depletion. Use with caution in patients taking diuretics or ACEI’s

A

Lithium carbonate

186
Q

Adequate sodium and fluid (2500 - 3500 mL) intake should be maintained. This drug has a narrow therapeutic index

A

Lithium carbonate

187
Q

AE’s include hand tremor, nausea, and mild thirst during initial therapy. Toxicity is manifested by DIARRHEA, VOMITING, DROWSINESS, muscular weakness & lack of coordination followed by BLURRED VISION, TINNITUS, and extreme polyuria

A

Lithium carbonate

188
Q

Effects may not be seen at once - may take 1 - 2 weeks before optimum effect is seen. Maintain your normal diet and have a fluid intake of 2 - 3 quarts a day during therapy. Avoid overexposure to heat and sweating during therapy.

A

Lithium carbonate

189
Q

Triamcinolone Acetonide (topical)

A

Kenalog

190
Q

AE’s include local burning, itching, and skin atrophy. AE’s occur more frequently when an occlusive dressing is used

A

Triamcinolone acetonide

191
Q

Doxazosin Mesylate

A

Cardura (XL)

192
Q

Selective antagonist of postsynaptic alpha-1 adrenergic receptors. This action results in dilation of arterioles and veins which leads to decreased peripheral resistance and decreased BP. Diastolic BP is affected more than systolic BP.

A

Doxazosin

193
Q

Caution should be used when given with other antihypertensive agents to avoid the possibility of significant hypotension

A

Doxazosin

194
Q

To decrease the risk or syncope at the initiation of therapy, all patients should be started with 1 mg tablets given at bedtime

A

Doxazosin

195
Q

Take XL form in the morning with breakfast. The insoluble shell of the XL tablet may be noticed in the stool

A

Doxazosin

196
Q

Take first dose of IR tablets at bedtime to avoid fainting - advise patients to rise slowly from a sitting or lying position

A

Doxazosin

197
Q

Avoid activities that require alertness for 12 hours following initial dose or dosing increases

A

Doxazosin

198
Q

Fluticasone propionate (inhalation)

A

Flovent

199
Q

CI in primary treatment of status asthmaticus. Use caution in patients who are being transferred from systemic corticosteroids to Flovent bc deaths due to adrenal insufficiency have occurred during and after transfer to aerosolized steroids. Not to be regarded as a bronchodilator and should not be given for rapid relief of bronchospasm

A

Fluticasone propionate (inhalation)

200
Q

Not intended to provide immediate relief of bronchospasm. To receive the full benefits of therapy, use on a regular basis. Although benefits can be seen after 2 days of treatment, up to 4 weeks may be needed to observe benefits.

A

Fluticasone propionate (inhalation)

201
Q

Follow instructions for technique: shake inhaler, breathe out fully, breathe medicine in deeply and slowly, hold breath as long as possible, breathe out gently, wait 1 min between puffs and repeat, rinse mouth after use, clean the inhaler at least once a day with warm water.

A

Fluticasone propionate (inhalation)

202
Q

Olmesartan Medoxomil

A

Benicar

203
Q

A prodrug that is hydrolyzed to olmesartan during absorption from the GI tract. Works as an ARB

A

Olmesartan

204
Q

Most common AE seen during therapy is dizziness (3%).

A

Olmesartan

205
Q

Butalbital, APAP, & Caffeine

A

Fioricet

206
Q

APAP produces analgesia by inhibiting prostaglandin synthesis in the CNS and through a peripheral action of blocking pain impulse generation. Butalbital produces sensory cortex depression through inhibition of conduction in the reticular formation at the level of the thalamus. Caffeine produces CNS stimulation by inhibition of phosphodiesterase which increases the accumulation of cAMP.

A

Fioricet

207
Q

CI in patients with porphyria

A

Fioricet

208
Q

Amoxicillin with Clavulanate Potassium

A

Augmentin (XR)

209
Q

Amoxicillin is a bacteriocidal antibiotic which inhibits bacterial cell wall synthesis via acylation of a transpeptidase enzyme. Clavulanic acid binds competitively to the active sites of beta-lactamase enzymes, thereby protecting PCNs and cephalosporins from destruction

A

Augmentin

210
Q

Since both Augmentin 250 and 500 tablets contain 125 mg clavulanic acid, two Augmentin 250 tablets do not equal one 500 tablet.

A

Augmentin

211
Q

Preferably taken at the start of a meal to enhance absorption and decrease GI upset. Take at even intervals, preferably around the clock. Follow chewable tablets with a full glass of water. Keep suspension refrigerated, discard after 10 days.

A

Augmentin

212
Q

APAP with Codeine

A

Tylenol w/codeine, Phenaphen w/codeine

213
Q

APAP produces analgesia by inhibiting prostaglandin synthesis in the CNS and through a peripheral action by blocking pain impulse generation. Codeine phosphate produces analgesia centrally via action on the central opiate receptors

A

APAP with codeine

214
Q

Use with caution in patients with increased ICP, head injury, severe hepatic or renal impairment, Addison’s disease, hypothyroidism, prostatic hypertrophy or urethral stricture, and in the presence of acute abdominal conditions

A

APAP with codeine

215
Q

Insulin Detemir

A

Levemir

216
Q

Unopened vials should be stored in the refrigerator. Do not freeze. Can be kept at room temperature for 42 days

A

Insulin Detemir

217
Q

Valsartan with HCTZ

A

Diovan-HCT

218
Q

Valsartan blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor found in many tissues (ARB). HCTZ inhibits the reabsorption of sodium and chloride at the distal renal tubule

A

Valsartan with HCTZ

219
Q

CI in patients with anuria or who are hypersensitive to sulfonamide-derived drugs.

A

Valsartan with HCTZ, Losartan with HCTZ

220
Q

Oxcarbazepine

A

Trileptal

221
Q

May produce its antiseizure activity by blockade of voltage-sensitive sodium channels, resulting in stabilization of hyper excited neural membranes, inhibition of repetitive neuronal firing, and diminution of propagation of synaptic impulses

A

Oxcarbazepine

222
Q

Approximately 25 - 30% of patients who have hypersensitivity to carbamazepine will have similar reactions to this drug

A

Oxcarbazepine

223
Q

Clinically significant hyponatremia can occur with this drug

A

Oxcarbazepine

224
Q

Most common AE’s are dizziness, somnolence, diplopia, fatigue, N/V, ataxia, abnormal vision, abdominal pain, tremor, dyspepsia, and abnormal gait

A

Oxcarbazepine

225
Q

Ondansetron HCl

A

Zofran

226
Q

A selective 5-HT3 receptor antagonist. Serotonin 5-HT3 receptors can be found peripherally on vagal nerve terminals and centrally in the chemoreceptor trigger zone of the area postrema

A

Ondansetron

227
Q

Not a drug that stimulates gastric or intestinal peristalsis (should not be used instead of nasogastric suction). Chewable tablets contain phenylalanine; use caution in phenylketonurics

A

Ondansetron

228
Q

AE’s include HA (25%), fatigue (10%), and constipation (8%)

A

Ondansetron

229
Q

Do not remove chewable tablets from the blister until just prior to use. Do not try to push the tablet through the foil, peel the blister apart to remove.

A

Ondansetron

230
Q

Ezetimibe with Simvastatin

A

Vytorin

231
Q

A class of lipid-lowering compounds that selectively inhibits the intestinal absorption of cholesterol and related phytosterols.

A

Ezetimibe with Simvastatin

232
Q

CI in patients with active liver disease or unexplained persistent elevations of serum transaminases. May cause optic nerve degeneration

A

Ezetimibe with Simvastatin

233
Q

Avoid grapefruit and grapefruit juice when taking this medication. Avoid overexposure to sunlight due to possibility of photosensitivity

A

Ezetimibe with Simvastatin

234
Q

Losartan Potassium with HCTZ

A

Hyzaar

235
Q

This drug and its principal active metabolite block the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor found in many tissues. The second part of this drug inhibits the reabsorption of sodium and chloride at the distal renal tubule

A

Losartan with HCTZ

236
Q

Most common AE’s are upper respiratory infection, dizziness, cough, and back pain

A

Losartan with HCTZ

237
Q

Budesonide & Formoterol Fumarate Dihydrate

A

Symbicort

238
Q

A LABA and a corticosteroid combination

A

Budesonide/Formoterol

239
Q

Budesonide is a potent anti-inflammatory corticosteroid that shows inhibitory activities against multiple cell types (mast cells, eosinophils, neutrophils, macrophages, lymphocytes) and mediators (histamine, eicosanoids, leukotrienes, cytokines).

Formoterol is a long-acting selective beta-2 adrenergic agonist which acts locally in the lung as a bronchodilator.

A

Symbicort

240
Q

CI in primary treatment of status asthmaticus

A

Symbicort

241
Q

LONG-ACTING BETA-2 AGONISTS INCREASE THE RISK OF ASTHMA-RELATED DEATH

A

Symbicort

242
Q

Secondary fungal infections of the oral cavity may occur and may require antifungal treatment

A

Symbicort

243
Q

Rinse mouth after each use

A

Symbicort

244
Q

To receive full benefits of therapy, use on a regular basis. Although benefits can be seen after 2 days of treatment, up to 4 weeks may be needed to observe benefits.

A

Symbicort