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  • 7/31/2019 Common Medication List - Moser

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Lactulose, Kristalose

    Synthetic disaccharide used

    for constipation. Bacteria in

    the colon degrade lactulose

    into lactic acid and formic

    acid which causes increase in

    osmotic pressure which in

    turn, softens the stool by

    promoting stool water

    content.

    Constipation. Hepatic

    encephalopathy:

    treatment and

    prophylaxis

    Improves GI motility so monitor the

    bowel movements. Monitor serum

    electrolytes (K, Cl, and CO2)

    Low-glucose diet

    requirement

    GI: bloating, diarrhea,

    epigastric pain, flatulence,

    nausea, vomiting

    Muscle: Cramps

    Endrocrine:

    Hypernatremia,

    Hypokalemaia

    Colace

    Docusate

    Draws liquid into the colon

    and thus softening the stool.

    Constipation Care Decrease abd discomfort and pain

    Bowel movement 12-72 hours

    Reassess if rectal bleeding or no

    bowel movement after laxative

    Hypersensitivity to

    docusate products.

    Concomitant use of

    mineral oil.

    Intestinal

    obstruction

    Acute abd pain with

    N/V

    Abnormal taste in the

    mouth (Bitter)

    Nausea

    Muscle cramps

    Polyethylene Glycol 3350

    Miralax

    Is an osmotic agent that

    causes retention of water in

    the stool which increases

    bowel movements. It

    appears to have no effect on

    active absorption or

    secretion of glucose or

    electrolytes

    Constipation Decrease abd pain and discomfort

    Bowel movement 2 to 4 days

    Check electrolyte imbalance after

    prolonged use.

    Hypersensitivity to

    any component such

    as polyethylene

    glycol

    Bowel obstruction

    Diarrhea, Flatulence,

    nausea, stomach cramps,

    swollen abd

    Amoxicillin/ clavulanate

    Augmentin

    Semisynthetic beta-lactam

    antibiotic. Clavulanic acid, a

    beta-lactamase inhibitor,

    protects amoxicillin against

    degradation and extends the

    antibiotic spectrum

    compared to amoxicillin

    alone.

    Acute otitis

    Pneumonia

    Lower resp tract

    infections

    UTI

    Sinusitis

    CBC to monitor pts response

    Culture treatment to ensure

    bacteria are sensitive to PCNs

    Hepatic function, in these patients

    check at regular intervals

    PCN allergies

    Hemodialysis pts

    Severe renal

    impairment

    Skin: diaper rash

    GI: diarrhea, loose stool,

    N/V

    Reproductive: Mycosis

    vaginitis

    Other: Candidiasis

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Trimethoprim-

    sulfamethoxazole

    Bactrim

    Sulfamethoxalzole is an

    antibacterial sulfonamide

    that prevents the formation

    of dihydrofolic acid, blocking

    bacterial synthesis. It

    interferes with the

    production of folic acid.

    Acute infective

    exacerbation of COPD

    HIV Pneumocystis

    pneumonia

    Travelers diarrhea

    UTI

    Shigellosis

    Watch for fever and check the CBC

    counts.

    Monitor Renal function

    Serum K, especially in elderly, HIV

    pts, and is also known to cause

    hyperkalemia

    Allergies to

    sulfonamides

    Infants less than 2

    months

    Hepatic damage

    Pregnant or nursing

    mothers

    Renal dysfunction

    Skin: Rash, Uticaria.

    GI:N/V

    Dermatologic: Erythema

    multiforme (SStevens-

    Johnson syndrome

    Hepatic: Hepatic necrosis

    Flonase/Fluticasone

    Propionate

    Acts as an anti-inflammatory

    as a human glucocorticoid

    receptor agonist

    Allergic rhinitis,

    Asthma, Atopic

    dermatitis, Disorder of

    skin, corticosteroid-

    responsive dermatoses,

    and non-allergic rhinitis

    (off label nasal polyp

    and vitiligo)

    -Resp: Lung sounds, pulmonary

    function tests during and several

    months after change from systemic

    to inhalation corticosteroids

    -Withdrawal symptoms from oral

    corticosteroids: depression, pain in

    joints, fatigue

    -Safety Alert! Adrenal Insufficiency:

    nausea, weakness, fatigue,hypotension, hypoglycemia,

    anorexia; may occur when

    changing from systemic to

    inhalation; may be life threatening;

    adrenal function tests periodically:

    hypothalamic-pituitary-adrenal axis

    suppression in long-term treatment

    -growth rate in children

    Hypersensitivity to

    the drug or to milk

    proteins, and

    primary treatment

    of status

    asthmaticus or

    other forms of

    asthma requiring

    and inhaler.

    Candidiasis of mouth and

    esophagus, headache,

    bronchitis, cough,

    epistaxis, inflammatory

    disorder of upper

    respiratory tract, sinusitis,

    throat irritation, and upper

    respiratory infection are

    the most common. Seriousside effects include

    secondary hypocortisolism,

    anaphylaxis, immune

    hypersensitivity reaction,

    glaucoma, and pneumonia

    Allegra/ Fexofenadine

    Hydrochloride

    Inhibits release of histamine

    from mast cells and

    selectively antagonizes

    peripheral histamine-

    receptor activity.

    Chronic idiopathic

    urticarial and seasonal

    allergic rhinitis. (Off-

    label: hymenoptera

    immunotherapy

    pretreatment and

    perennial allergic

    rhinitis)

    -Allergy: itchy, runny, watery eyes;

    congested nose; before and during

    treatment

    -I&O: be alert for urinary retention,

    frequency, dysuria, esp. geriatric

    pts; product should be

    discontinued if these occur, serum

    creatinine/BUN baseline and

    periodically during treatment

    -Resp: rate, rhythm, increase in

    bronchial secretions, wheezing,

    chest tightness

    Hypersensitivity Indigestion, dizziness,

    headache, somnolence,

    otitis media,

    dysmenorrhea, upper

    respiratory infection,

    fatigue, viral disease, cold,

    and flu

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Zyrtec/ Cetirizine

    Hydrochloride

    An antihistamine that

    selectively inhibits the effect

    of peripheral H1-receptors; a

    human metabolite of

    hydroxyzine

    Perennial and seasonal

    allergic rhinitis, and

    chronic urticaria (off-

    label: adjunct asthma,

    atopic dermatitis, and

    acute urticaria)

    -Allergy symptoms: pruritus,

    urticaria, watering eyes, baseline

    and during treatment

    -Resp: rate, rhythm, increase in

    bronchial secretions, wheezing,

    chest tightness

    -Blood studies: LFTs, BUN,

    creatinine baseline, periodically

    Hypersensitivity to

    cetirizine,

    levocetirizine, or

    hydroxyzine

    Xerostomia, headache,

    somnolence, and fatigue.

    Benadryl/

    Diphenhydramine

    Hydrochloride

    Acts as an antihistamine by

    competing with histamine

    for receptor cites on effector

    cells

    Allergic rhinitis,

    anaphylaxis, common

    cold, insomnia, motion

    sickness, Parkinsons,

    and pruritus of skin

    (off-label:

    chemotherapy,

    extrapyramidal disease,

    hyperemesis

    gravidarum, local

    anesthesia)

    -Be alert for urinary retention,

    frequency, dysuria; product should

    be discontinued

    -CBC during long-term therapy;

    blood dyscrasias may occur

    -Resp: rate, rhythm, increase in

    bronchial secretions, wheezing,

    chest tightness

    Hypersensitivity,

    newborn/premature

    infants, and nursing

    mothers

    Xerostomia, dizziness,

    dyskinesia, sedative

    effects, somnolence, dry

    nasal mucosa, pharyngeal

    dryness, thick sputum, and

    anaphylaxis

    Fentanyl Systemically produces effects

    via agonist actions at the mu

    receptor. May cause

    respiratory depression.

    Increases tone and decreases

    contractions of smooth

    muscle of GI tract.

    Transdermally acts with

    opiod mu-receptors in CNS

    causing analgesia, mood

    alterations, euphoria,

    dysphoria, and drowsiness.

    Constricts the pupils. Alters

    perception of and emotional

    response to pain.

    Moderate to severe

    chronic pain that

    cannot be managed by

    other means in a

    patient who is opioid

    tolerant. (Off-label:

    moderate to severe

    osteoarthritis with an

    inadequate response

    with a weak opioid

    analgesic therapy)

    -VS after parenteral route; note

    muscle rigidity, drug history,

    hepatic and renal function tests

    -CNS: dizziness, drowsiness,

    hallucinations, euphoria, LOC, pupil

    reaction

    -Allergic reaction: rash, urticaria

    -Resp: respiratory depression,

    character, rate, rhythm; notify

    prescriber if respirations < 10/min

    MAY CAUSE

    RESPIRATORY

    DEPRESSION.

    Acute or

    postoperative pain,

    risk of life-

    threatening

    hypoventilation,

    acute or severe

    bronchial asthma.

    Hypersensitivity.

    Mild or intermittent

    pain management.

    Opioid non-tolerant

    patients. Suspected

    or known paralytic

    ileus. Should not be

    used on children.

    Potential for abuse due to

    opioid-like effects.

    Application site reactions,

    pruritus, sweating,

    abdominal pain,

    constipation, diarrhea,

    indigestion, nausea,

    vomiting, xerostomia,

    asthenia, confusion,

    dizziness, nervousness,

    headache, insomnia,

    somnolence, anxiety,

    depression, euphoria,

    hallucinations, urinary

    retention, upper

    respiratory infection, and

    fatigue. Serious side effects

    include bradyarrhythmia,

    cardiac dysrhythmia, chest

    pain, apnea, dyspnea,

    respiratory depression.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Solu Medrol/

    Methylprednisolone

    Anti-Inflammatory Rheumatoid Arhritis

    Psoriatic Arthritis

    Ulcerative Colitis

    Crohns Disease

    Serum Sickness

    Transfusion Rxn

    Stevens-Johnson

    syndrome

    Acute Asthma

    Monitor:

    Electrolyte Balance

    BP

    Weight

    Urinalysis

    Chest X-rays needed if treatment >

    6wks

    Give at smallest dose possible

    Osteoporosis or risk

    of

    Systemic fungal

    infection

    Fluid retention

    Wight Gain

    High BP

    Hirutism

    Headache

    Weakness

    Photosensitivity

    Ulcers

    Convulsions

    Euphoria

    Insomnia

    Albuterol Bronchodilator Asthma

    Exercise induced

    asthma

    Chronic Bronchitis

    Emphysema

    None Recommended PT Hypersensitive to

    drug class

    Ischemic Heart

    Disease

    Hypertension

    ArrhythmiasHyperthyroidism

    Epilepsy

    Nervousness

    Tremors

    Headache

    Palpitations

    High BP

    DizzinessNausea

    Xopenex/ Levalbuterol Bronchodilator Asthma

    Exercise induced

    asthma

    COPD

    None Recommended PT Hypersensitive to

    drug class

    PT on Monoamine

    oxidase inhibitor

    medication

    Nervousness

    Tremors

    Headache

    Palpitations

    High BP

    Dizziness

    Nausea

    Advair/ Combination of

    Flucticasone and Salmerol

    Bronchodilator Asthma Maintenance

    COPD

    Bone Density if Osteoporotic

    Oral Cavity Inspection

    Monitor for Vision Changes, child

    development

    PT Hypersensitive to

    Atropine

    Narrow Angle

    Glaucoma

    Prostatic

    Hypertrophy

    Allergies to Milk

    Proteins

    Headache

    Sore Throat

    Sinus Inflammation

    N/V

    Bronchitis

    Dizziness

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Atrovent/ Ipratropium Bronchodilator

    Prophylactic

    COPD

    Chronic Bronchitis

    Emphysema

    None Recommended PT Hypersensitive to

    Atropine

    Narrow Angle

    Glaucoma

    Prostatic

    Hypertrophy

    Urinary system

    obstruction

    Dizziness

    Nausea

    Heartburn

    Constipation

    Dry mouth

    Back pain

    Difficulty urinating

    Pain when urinating

    frequency

    Aspirin

    Blocks pain impulses in CNS,

    reduces inflammation by

    inhibition of prostaglandin

    synthesis; antipyretic action

    results from vasodilation of

    peripheral vessels; decreases

    platelet aggregation

    Mild to moderate pain

    or fever including RA,

    osteoarthritis, TIA,

    thromboembolic

    disorders, rheumatic

    fever, post MI,

    prophylaxis of MI,

    ischemic stroke,

    angina, acute MI,

    Pain: character, location, intensity;

    ROM-before and 1 hr after

    administration.

    Fever: temperature before and 1 hr

    after administration.

    Hepatic studies: AST, ALT, bilirubin,

    creatinine if pt is on long-term

    therapy.

    Renal Studies: BUN, urine

    creatinine; I&O ratio; decreasing

    output may indicate renal failure.

    Blood studies: CBC, Hct, Hgb, PT if

    patient is on long-term therapy.

    Allergic RXN: rash, urticaria,.

    Ototoxicity: tinnitus, ringing,

    roaring in ears.

    Edema in feet, ankles, legs.

    Pregnancy (D) 3rd

    trimester,

    breastfeeding,

    children

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Lovenox

    Prevents conversion of

    prothrombin to thrombin

    and prevents fibrin from

    further converting to

    thrombin.

    Prevention of DVT, PE

    (inpatient) in hip and

    knee replacement,

    abdominal surgery at

    risk for thrombosis;

    unstable angina/non Q

    wave MI.

    Blood studies: Hct, Hgb, CBC,

    coagulation, platelets, occult blood

    ins tools, anti-factor Xa.

    Renal studies: BUN/creatinine

    baseline and periodically.

    Bleeding: gums, petechiae,

    ecchymosis, black tarry stools,

    hematuria

    Neuro symptoms in patients who

    have received spinal anesthesia.

    Active major

    bleeding;

    thrombocytopenia

    with a positive in

    vitro test for anti-

    platelet antibody in

    the presence of

    enoxaparin sodium;

    known

    hypersensitivity to

    enoxaparin sodium,

    heparin, pork

    products, or benzyl

    alcohol (multi-dose

    formulation only)

    Hemorrhage, hypochromic

    anemia,

    thrombocytopenia,

    bleeding. Fever confusion,

    nausea, ecchymosis,

    hyperkalemia in renal

    failure, edema, peripheral

    edema; allergic reaction:

    hives; difficulty breathing;

    swelling of face, lips,

    tongue, or throat. Bleeding

    that wont stop;

    pale skin, easy bruising,

    unusual weakness;

    swelling, bruising or

    swelling in one or both

    legs.

    Prilosec

    Gastric acid pump inhibitor-

    Suppresses gastric acid (H+

    ion) secretion by blocking

    the hydrogen/potassium ATP

    ase pump (proton pump) of

    the gastric parietal cells

    which secrete H+ directly

    into the gastric lumen.

    Duodenal ulcer, gastric

    ulcer, gastro-

    esophageal reflux

    disease (GERD);

    maintain healing of

    erosive esophagitis;

    long-term treatment of

    pathological

    hypersecretory

    conditions in adults.

    GI system: bowel sounds q8hr,

    abdomen for pain, swelling,

    anorexia, blood in stools.

    Hepatic enzymes: AST, ALT, alkaline

    phosphatase during treatment;

    blood studies: CBC, differential

    during treatment, blood dyscrasias

    may occur.

    Seious skin rxns: toxic epidermal

    necrolysis, Stevens-Johnson

    syndrome, angioedema, exfoliativedermatitis; fever, sore throat,

    fatigue, thin ulcers, lesions in

    mouth, lips.

    Known

    hypersensitivity.

    Pregnancy (C),

    breastfeeding,

    children.

    Heart Failure, hepatic

    failure, proteinuria,

    hematuria, pancytopenia,

    leukocytosis, pneumonia,

    angioedema, exfoliative

    dermatitis, Stevens-

    Johnsons Syndrome, toxic

    epidermal necrolysis.

    Headache, dizziness,

    asthenia, diarrhea,

    abdominal pain, vomiting,nausea, constipation,

    flatulence, acid

    regurgitation, rash, back

    apin, upper respiratory

    infections, cough. Tinnitus,

    taste perversion, chest

    pain, palpitations,

    tachycardia, bradycardia,

    peripheral edema,

    abdominal swelling,

    anorexia, irritable colon,

    dry mouth, UTI, urinary

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Prilosec cont.

    frequency, dry skin,

    urticaria, pruitis, alopecia,

    hypoglycemia, weight gain,

    fever, fatigue, malaise.

    Synthroid/Levothyroxine

    Sodium

    Thyroid replacement

    hormone; mechanism not

    established. Suspected that

    principal effects are exerted

    through control of DNA

    transcription and protein

    synthesis.

    Replacement or

    supplemental therapy

    in congenital or

    acquired

    hypothyroidism during

    recovery phase of

    subacute thyroiditis.

    Treatment or

    prevention of various

    types of euthyroid

    goiters, including

    thyroid nodules,

    subacute or chroniclymphocytic thyroiditis,

    multinodular goiter and

    as an adjunct to

    surgery and radioiodine

    therapy for

    thyrotropin-dependent

    well-differentiated

    thyroid cancer.

    Assess for untreated subclinical or

    overt thyrotoxicosis, acute MI,

    uncorrected adrenal insufficiency,

    age, CAD, CV disorders, nontoxic

    diffuse goiter, nodular thyroid

    disease, DM, hypersensitivity,

    pregnancy/nursing status, and for

    possible drug interactions. In

    patients w/ secondary or tertiary

    hypothyroidism, assess for

    additional hypothalamic/pituitary

    hormone deficiencies. Assess for

    weight and TSH levels. In infantswith congenital hypothyroidism,

    assess for congenital anomalies.

    Untreated

    subclinical

    (suppressed serum

    TSH level with

    normal T3 level and

    T4 levels) or overt

    thyrotoxicosis of any

    etiology, acute MI,

    and uncorrected

    adrenal

    insufficiency.

    Fatigue, increase appetite,

    weight loss, heat

    intolerance, headache,

    hyperactivity, irritability,

    insomnia, palpitations,

    arrhythmias, dyspnea, hair

    loss, menstrual

    irregularities,

    pseudotumor cerebri

    (children), slipped capital

    femoral epiphysis

    (children).

    Plavix/Clopidogrel

    Bisulfate

    Platelet activation and

    aggregation inhibitor;

    irreversibly and selectivelyinhibits the binding of ADP to

    its platelet P2Y12 receptor

    and subsequent ADP-

    mediated activation of the

    glycoprotein GPIIb/IIIa

    complex.

    To decrease the rate of

    combined endpoint of

    CV death, MI, stroke, orrefractory ischemia in

    pts w/ non-ST-segment

    elevation ACS,

    including those who

    are managed medically

    and those w/ coronary

    revascularization. To

    reduce rate of death

    from any cause and the

    rate of combined

    endpoint of death, re-

    infarction, or stroke in

    Assess for presence of active

    pathological bleeding, previous

    hypersensitivity to the drug,reduced CYP2C19 function,

    pregnancy/nursing status, and

    possible drug interactions. Assess

    use in pts at risk for increase

    bleeding (eg, undergoing surgery).

    Active pathological

    bleeding (eg, peptic

    ulcer, intracranialhemorrhage).

    TTP, bleeding, epistaxis,

    hematuria, bruising,

    hematoma, pruritus.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Plavix/Clopidogrel

    Bisulfate

    Cont.

    patients with

    ST_elevation MI. To

    reduce rate of

    combined endpoint of

    new ischemic stroke or

    MI, and other vascular

    deaths in pts with hx of

    recent MI or stroke, or

    established PAD.

    Vancomycin/Vancomycin

    HCl

    Tricyclic glycopeptide

    antibiotic; inhibits cell-wall

    biosynthesis, alters bacterial

    cell membrane permeability

    and RNA synthesis.

    Treatment of serious or

    severe infections

    caused by susceptible

    strains of methicillin-

    resistant staphylococci.

    Indicated for PCN-

    allergic pts who cannot

    receive or have failed

    to respond to other

    drugs, and for

    infections caused by

    vancomycin-susceptible

    organisms that are

    resistant to other

    antimicrobials.

    Assess for renal function,

    underlying hearing loss,

    pregnancy/nursing status and

    possible drug interactions. Perform

    culture and susceptibility testing.

    Contraindicated for

    pts with known

    hypersensitivity to

    this product, renal,

    and auditory

    susceptibility/insuffi

    ciency.

    Infusion-related events,

    hypotension, wheezing,

    pruritus, chest and back

    muscle spasm or pain,

    dyspnea, urticaria,

    nephrotoxicity,

    pseudomembranous

    colitis, ototoxicity,

    neutropenia, phlebitis.

    Maxipime/Cefepime HCl 4th generation

    cephalosporin; bactericidal

    agent that acts by inhibiting

    cell wall synthesis.

    Treatment of

    uncomplicated/complic

    ated UTI including

    pyelonephritis,

    uncomplicated skin and

    skin structure,

    complicated intra-

    abdominal infections,

    and pneumonia caused

    by susceptible strains

    of microorganisms.

    Empiric therapy for

    febrile neutropenia.

    Assess for PCN allergy,

    pregnancy/nursing status, history

    of GI disease, renal/hepatic

    impairment, nutritional status, and

    possible drug interactions.

    Document indications for therapy

    with culture and susceptibility

    testing. (Generic): Assess for allergy

    to corn or corn products.

    Hypersensitivity to

    penicillins or other

    beta-lactam

    antibiotics.

    Local reactions (eg,

    phlebitis), rash, diarrhea,

    (+) Coombs test (without

    hemolysis).

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Zyvox/Linezolid Oxazolidinone antibacterial;

    inhibits bacterial protein

    synthesis; bids to a site on

    the bacteria 23S ribosomal

    RNA of the 50S subunit and

    prevents formation of

    functional 70S initiation

    complex, which is an

    essential component of the

    bacterial translation process.

    Treatment of

    vancomycin-resistant

    Enterococcus faecium

    (VRE) infections

    including cases with

    concurrent bacteremia,

    nosocomial

    pneumonia,

    complicated skin and

    skin structure

    infections (SSSI)

    including diabetic food

    infections without

    concomitant

    osteomyelitis,

    uncomplicated SSSI,

    community-acquired

    pneumonia (CAP)including concurrent

    bacteremia caused by

    susceptible strains of

    designated

    microorganisms.

    Assess for pre-existing

    myelosuppression (including

    anemia, leukopenia, pancytopenia,

    thrombocytopenia), concomitant

    drugs that produce

    myelosuppression, presence of

    chronic infections, previous or

    concomitant antibiotic therapy,

    catheter-related bloodstream

    infections or catheter-site

    infections, pregnancy/nursing

    status, uncontrolled HTN, carcinoid

    syndrome, pheochromocytoma,

    untreated hyperthyroidism,

    phenylketonuria, renal/hepatic

    impairment, and possible drug

    interactions.

    MAOIs A or B (eg

    phenelzine,

    isocarboxazid) or

    within two weeks

    after taking such

    drugs; uncontrolled

    HTN,

    pheochromocytoma

    , thyrotoxicosis,

    and/or taking

    directly and

    indirectly acting

    sympathomimetic

    agents, vasopressive

    agents,

    dopaminergic

    agents; carcinoid

    syndrome and/ortaking SSRIs, TCAs,

    serotonin 5-HT1

    receptor agonists,

    meperidine or

    buspirone.

    Diarrhea, headache, N/V,

    fever, sepsis, anemia,

    thrombocytopenia, upper

    respiratory infection,

    trauma.

    Lisinopril

    Angiotensin-converting

    enzyme (ACE) inhibitor.

    Blocks conversion of

    angiotensin I tovasoconstrictor angiotensin

    II. Prevents degradation of

    bradykinin and other

    vasodilatory prostaglandins.

    Incr plasma renin levels and

    decr aldosterone levels. Net

    result = systemic

    vasodilation.

    Hypertension, heart

    failure, reduce risk of

    dealth or heart failure

    after MI. Lowers BP.

    Monitor BP and pulse frequently,

    esp during initial dose adjustment.

    Monitor freq of Rx refills to

    determine compliance. Assess for

    signs of angioedema (dyspnea,

    facial swelling). To prevent heart

    failure, monitor weight and assess

    pt routinely for resolution of fluid

    overload (peripheral edema,

    rales/crackles, dyspnea, wt gain,

    jugular venous distention). Monitor

    renal function. May cause incr in

    BUN & serum creatinine. May

    cause hyperkalemia. Monitor CBC

    for pts w/ collagen vascular dx &/or

    renal dx. May cause elevated AST,

    Family hx of

    angioedema. Pt hx

    of angioedema w/

    previous ACE

    inhibitors.

    Hypersensitivity.

    Pregnancy Category

    C (1st trimester),

    Category D (2nd/3rd

    trimesters).

    Breastfeeding

    (appears in breast

    milk). Use caution:

    Pts w/ renal

    impairment,

    hypovolemia,

    Angioedema. CNS:

    dizziness, fatigue, HA,

    weakness. Resp: cough.

    CV: hypotension, chest

    pain. GI: abdominal pain,

    N/V, diarrhea. GU: erectile

    dysfunction, impaired

    renal function. Derm:

    rashes. F&E hyperkalemia.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Lisinopril cont.

    ALT, alkaline phosphatase & serum

    bilirubin.

    hyponatremia,

    concurrent diuretic

    therapy. Incr risk of

    angioedema in black

    pts & monotherapy

    less effective in

    black pts (may

    require addl

    therapy).

    Surgery/anesthesia

    (hypotension may

    be exaggerated).

    Safety not

    established-children

    < 6yr. Geriatric:

    initial dosage

    reduction

    recommended.

    Metoprolol

    (Lopressor)

    Beta-Blocker

    Beta-adrenergic antagonist-

    block SNS

    catecholamines..reduced

    renin & aldosterone release

    & fluid balance..vasodilation

    of arterioles to decr

    pulmonary vascular

    resistance and blood

    pressure.

    Antihypertensive ACE

    inhibitor. Hypertension,

    antianginal in long term

    tx of angina.

    Dysrhythmias (to

    suppress sinus and

    atrial tachy-dysrhythmias) Beta1

    (cardioselective)

    metopropol (Lopressor,

    Toprol XL) used for

    angina and

    hypertension

    VS assess BP before & after initial

    dose. Monitor closely if given w/ a

    Calcium channel blocker.

    Report any weakness, dizziness,

    fainting, edema or difficultybreathing. If SBP is below

    90mm/Hg or for bradycardia, notify

    HC provider.

    Pts w/ DM: tachycardia (a symp of

    hypoglycemia) is often masked due

    to beta1 blockade.

    Atrioventricula (AV)

    block,

    bradydysrhythmias.

    Bradycardia,hypotension. May

    interact w/

    hypoglycemic

    agents- use caution

    in pt w/ DM.

    Orthostatic hypotension,

    bradycardia, drowsiness,

    decreased libido.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Metoclopramide

    Hydrochloride (Reglan)

    Suppresses emesis by

    blocking dopamine receptors

    in the chemoreceptor trigger

    aone. Increases tone and

    accelerates intestinal transit

    & gastric emptying by

    enhancing action of ACh.

    Peristaltic stimulant,

    antiemetic

    Monitor renal function, BP and

    heart rate. Assess hydration.

    Monitor for anxiety restlessness,

    extrapyramidal symptoms. Monitor

    bowel response and therapeutic

    response. To prevent nausea,

    admin 30 pre chemotherapy. Also

    30 min before meals and at

    bedtime for gastroparesis.

    GI obstruction or

    perforation, GI

    hemorrhage. Dont

    use concurrently w/

    meds that cause

    extrapyramidal

    reactions (motor

    deficits, loss of

    postural reflexes,

    bradykinesia,

    tremor, rigidity,

    various involuntary

    movements.

    Drowsiness, restlessness,

    fatigue, lethargy, dizziness,

    HA, insomnia, dry mouth,

    extrapyramidal symptoms

    (toxic).

    Promethazine

    (Phenergan)

    Blocks histamine receptors in

    neuronal pathway, from

    vestibular apparatus to

    vomiting center in the

    medulla.

    Antiemetic,

    antihistamine.

    Evaluate pt respiratory status,

    teach pt to avoid tasks requiring

    mental alertness and to report

    tremors or abnormal body

    movements. Long-term therapy-

    check CBC. Watch for drowsiness,

    restlessness, hypotension,

    confusion, urinary retention.

    Severe CNS

    depression, acute

    asthma, glaucoma,

    GI or GU

    obstruction,

    pregnancy, seizures.

    Sedation, drowsiness,disorientation, syncope in

    geriatrics, hypotension, dry

    mouth, urinary retention,

    flushing, epigastric

    distress, visual and hearing

    disturbances.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Ondansetron

    (Zofran)

    (do not confuse with

    Zosyn!)

    Blocks effects of serotonin at

    5-HT3 receptor sites

    (selective antagonist) located

    in vagal nerve terminals &

    the chemoreceptor trigger

    zone in the CNS.

    Antiemetic. Prevent

    N/V associated w

    emetogenic

    chemotherapy or

    radiation therapy.

    Prevent and treat

    postoperative N/V.

    Assess for N/V, abdominal

    distention & bowel sounds prior to

    and following administration.

    Assess for extrapyramidal effects

    (involuntary movements, facial

    grimacing, rigidity, shuffling walk,

    trembling hands). Lab tests: may

    cause incr in serum bilirubin, AST &

    ALT levels.

    Orally disintegrating

    tablets contain

    aspartame and

    should not be given

    to pts w

    phenylketonuria.

    Concurrent use of

    apomorphine.

    Hypersensitivity.

    Use cautiously in:

    hepatic impairment

    (daily dose must be

    < 8mg), abdominal

    surgery (may mask

    ileus), Pregnancy

    (category B),

    lactation, or children

    3 or younger (PO) or

    < 1 mo (parenternal)

    (safety not

    established).

    CNS: HA, dizziness,

    drowsiness, fatigue,

    weakness. GI: constipation,

    diarrhea, abdominal pain,

    dry mouth, incr liver

    enzymes. Neuro:

    extrapyramidal reactions.

    Niravam, Xanax

    Alprazolam

    Depresses subcortical levelsof CNS, including limbic

    system, reticular formation

    Anxiety, panic

    disorders with orwithout agoraphobia,

    anxiety with depressive

    symptoms

    Monitor hepatic, blood studies

    Monitor BP lying, standing; pulse, if

    systolic pressure drops 20 mm Hg,hold product, notify prescriber

    Monitor mental status: anxiety,

    mood, drowsiness, dizziness,

    sleeping pattern, orientation and

    sensorium, especially in geriatric

    patients prior to and during

    treatment

    Monitor physical dependency,

    withdrawal symptoms, agitation,

    Pregnancy

    Breastfeeding

    Hypersensitivity to

    benzodiazepines

    Closed- angle

    glaucoma

    Psychosis

    Addiction

    Skin: Rash, dermatitis,

    itching

    GI: Constipation, dry

    mouth, nausea, vomiting

    anorexia, diarrhea, weight

    gain/ loss, increased

    appetite

    EENT: Blurred vision,

    tinnitus, mydriasis

    CV: Orthostatic

    hypotension, ECG changes,

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Niravam, Xanax

    Alprazolam cont.

    seizures, muscle pain, weakness,

    headache, panic attacks, nausea,

    vomiting

    tachycardia, hypotension

    CNS: Dizziness, drowsiness,

    confusion, headache,

    anxiety, tremors, fatigue,

    depression, insomnia,hallucinations, memory

    impairment, poor

    coordination

    Dilantin

    PhenytoinInhibits spread of seizure

    activity in motor cortex by

    altering ion transport;

    increases AV conduction

    Generalized tonic-

    clonic seizures; status

    epilepticus;

    nonepileptic seizures

    associated with Reyes

    syndrome or after head

    trauma; Bells palsy,

    complex partial

    seizures

    Monitor respiratory depression:

    rate, depth, character

    Monitor blood dyscrasias: fever,

    sore throat, bruising, rash, jaundice

    Monitor mental status: mood,

    sensorium, memory (long, short),

    suicidal thoughts/ behaviors

    Monitor purple glove syndrome

    with IV use

    Monitor skin disorders: rash that

    may lead to Stevens- Johnson

    syndrome or toxic epidermal

    necrolysis; phenytoin should not be

    used again

    Monitor temperature,

    lymphadenopathy; may cause

    hepatotoxicity, renal failure,

    rhabdomyolysis

    Pregnancy

    Hypersensitivity

    Psychiatric condition

    Bradycardia

    AV and SA block

    Stokes- Adams

    syndrome

    Hepatic failure

    CNS: Drowsiness, dizziness,

    insomnia, depression,

    suicidal tendencies,

    paresthesias, aggression,headache, confusion,

    slurred speech, peripheral

    neuropathy

    CV: Hypotension,

    ventricular fibrillation

    EENT: Nystagmus, diplopia,

    blurred vision

    ENDO: Diabetes insipidus

    GI: Nausea, vomiting,

    constipation, anorexia,

    weight loss, hepatitis,

    jaundice, gingival

    hyperplasia

    GU: Nephritis, urine

    discoloration

    Skin: Rash, hirsutism, toxic

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Dilantin

    Phenytoin cont.

    Acute intermittent

    porphyria

    epidermal necrolysis, lupus

    erythematosus, Stevens-

    Johnson syndrome

    SYST: Hypocalcemia,

    purple glove syndrome (IV)

    HEMA: Agranulocytosis,

    leucopenia, aplastic

    anemia, megaloblastic

    anemia thrombocytopenia,

    Topamax

    Topiramate

    May prevent seizure spread

    as opposed to an elevation

    of seizure threshold

    Partial seizures in

    adults and children 2-

    16 yr old; tonic- clonic

    seizures; seizures in

    Lennox- Gastaut

    syndrome, migraineprophylaxis

    Monitor renal and hepatic studies

    Monitor CBC during long- term

    therapy (anemia), metabolicacidosis

    Seizures- location, type, duration

    Migraines- pain location, duration,

    alleviating factor

    Bipolar disorder: mood, behavior

    Mental status: behavioral changes,

    suicidal thoughts/ behaviors,

    sensorium, body weight, evidence

    of cognitive disorder

    Hypersensitivity

    Metabolic acidosis

    CNS: Dizziness, fatigue,

    cognitive disorder,

    insomnia, anxiety,

    depression, paresthesia,memory loss, tremor,

    motor retardation, suicidal

    ideation

    EENT: Diplopia, vision

    abnormality

    GI: Diarrhea, anorexia,

    nausea, dyspepsia,

    abdominal pain,

    constipation, dry mouth,

    pancreatitis

    Skin: Rash

    GU: Breast pain,

    dysmenorrheal, menstrual

    disorder

    RESP: Upper respiratory

    tract infection, pharyngitis,

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Topamax

    Topiramate cont.

    sinusitis

    Misc: Weight loss,

    leukopenia, metabolic

    acidosis, increased body

    temperature, unexplaineddeath (epilepsy)

    Cerebyx, Prodilantin

    Fosphenytoin

    Inhibits spread of seizure

    activity in motor cortex by

    altering ion transport;increases AV conduction,

    prodrug of phenytoin

    Generalized tonic-

    clonic seizures status

    epilepticus, partial

    seizures

    Monitor seizure activity includingtype, location, duration; provide

    seizure precaution

    Monitor mental status: mood,

    memory (long, short), suicidal

    thoughts/ behaviors

    Toxicity: bone marrow depression,

    nausea, vomiting, ataxia, diplopia,

    cardiovascular collapse, slurred

    speech, confusion

    Respiratory depression: rate,

    depth, character of respirations

    Blood dyscrasias: fever, sore throat,

    bruising, rash, jaundice

    Monitor BP and ECG

    Pregnancy

    Hypersensitivity

    Psychiatric

    conditions

    Bradycardia

    SA and AV block

    Stokes- Adams

    syndrome

    CNS: Drowsiness,

    dizziness, insomnia,

    paresthesias, depression,

    suicidal tendencies,

    aggression, headache,

    confusion

    CV: Hypo/ hypertension,

    ventricular fibrillation,

    shock

    EENT: Nystagmus, diplopia,

    blurred vision

    GI: Nausea, vomiting,

    diarrhea, constipation,

    anorexia, weight loss,

    hepatitis, jaundice, gingival

    hyperplasia

    HEMA: Agranulocytosis,

    leukopenia, aplastic

    anemia,

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Cerebyx, Prodilantin

    Fosphenytoin cont.

    Absence seizures

    thrombocytopenia,

    megaloblastic anemia

    Skin: Rash, lupus

    erythematosus, Stevens-

    Johnson syndrome,hirsutism, hypersensitivity,

    pruritus

    SYST: Hyperglycemia,

    hypokalemia

    Nitro- Time, Nitro- Bid,

    Nitro- Stat, Nitro- Mist,Minitran, Nitro-Dur

    Nitroglycerine

    Decreases preload, afterload,

    which is responsible fordecreasing left ventricular

    end diastolic pressure,

    systemic vascular resistance;

    dilates coronary arteries,

    improves blood flow through

    coronary vasculature, dilates

    arterial, venous beds

    systemically

    Chronic stable angina

    pectoris, prophylaxis of

    angina pain, CHF acute

    MI, controlled

    hypotension in surgical

    procedures

    Monitor pain: duration, time

    started, activity being performed,

    character

    Orthostatic BP, pulse prior to and

    after administration

    Headache, light- headedness,

    decreased BP; may indicate a need

    for decreased dosage

    Tolerance if taken over long period

    Hypersensitivity to

    this product or

    nitrites, severeanemia, increased

    intracranial

    pressure, cerebral

    hemorrhage, closed-

    angle glaucoma,

    cardiac temponade,

    cardiomyopathy,

    constrictive

    pericarditis

    CNS: Headache, flushing,

    dizziness

    CV: Postural hypotension,

    tachycardia, collapse,

    syncope, palpitations

    GI: Nausea, vomiting

    Skin: Pallor, sweating, rash

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Morphine

    Brands: Astramorph PF,

    Avinza, Depo Dur,

    Infumorph PF, Kadian,

    M.O.S., MS Contin, MSIR,

    Oramorph SR, PMS-

    Morphine Sulfate, ratio-

    Morphine, ratio-

    Morphine SR

    Depresses pain impulse

    transmission at the spinal

    cord level by interacting with

    opioid receptors

    Moderate to severe

    pain

    Pain: Location, type, character -give before too severe Bowel

    function - constipation I&O - may

    cause urinary retention B/P, Pulse,

    Resp - character, depth, rate CNS -

    dizziness, drowsiness,

    hallucinations, euphoria, LOC, pupil

    rxn Allergic Rxn - rash, urticaria

    Respiratory dysfunction -

    depression, character, rate,

    rhythm, notify prescriber if

    resp

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Hydromorphone

    Brands: Dilaudid,

    Dilaudid HP, Exalgo,

    Hydromorph contin,

    PMS-Hydromorphone

    Inhibits ascending pain

    pathways in CNS, increases

    pain threshold, alters pain

    perception

    Moderate to severe

    pain, nonproductive

    cough

    Respiratory dysfunction

    depression, character, rate,

    rhythm, notify prescriber if resp

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Hydrocodone /

    Acetaminophen

    Brands: Anexsia, Co-

    Gesic, Hycet, Liquicet,

    Lorcet, Lorcet Plus,

    Lortab, Margesic H,

    Maxidone, Norco,

    Polygesic, Stagesic,

    Vanacet, Vicodin, Vicodin

    ES, Vicodin HP, Xodol,

    Zamicet, Zolvit, Zydone

    Acts directly on cough center

    in medulla to suppress

    cough; binds to opiate

    receptors in CNS to reduce

    pain

    Hyperactive and

    nonproductive cough,

    mild to moderate pain

    Pain: intensity, type, location, and

    other characteristics before and 1

    hr after giving product, titrateupward by 25% until pain is

    reduced by 1/2 CNS changes:

    dizziness, drowsiness,

    hallucinations, euphoria, LOC, pupil

    rxn B/P, Pulse, Resp:before and

    periodically, if resp < 10/min, dose

    may need to be reduced,

    oversedation may occur Bond

    Status: constipation, provide fluids,

    fiber in diet, may need stimulative

    laxative Allergic Rxn: rash, urticaria

    Cough and Resp.

    dysfunction:respiratory depression,

    character, rate, rhythm Need for

    pain medication, physical

    dependence, opioid is more

    effective before pain is severe

    Ance

    rosacea/vulgaris,

    Cushing's, measles,

    perioral dermatitis,

    varicella, abrupt

    discontinuation,

    hypersensitivity to

    this product or

    benzyl

    hypersensitivity

    CNS: drowsiness, dizziness,

    light-headedness,

    confusion, H/A, sedation,

    euphoria, dysphoria,

    weakness, hallucinations,

    disorientation, mood

    changes, dependence,

    seizures CV: palpitations,

    tachycardia, bradycardia,

    change in B/P,circulatory

    depression, syncope;

    cardiac arrest (children)

    EENT: tinnitus, blurred

    vision, miosis, diplopia GI:

    nausea, vomiting,

    anorexia, constipation,

    cramps, dry mouth, ulcersGU: Increased urinary

    output, dysuria, urinary

    retention INTEG: rash,

    urticaria, flushing, pruritus

    RESP: resp depression;

    pulmonary edema,

    bronchopneumonia, resp

    arrest (children)

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Hydrocodone Brands:

    Hycodan, Tussigon

    Acts directly on cough center

    in medulla to suppress

    cough; binds to opiate

    receptors in CNS to reduce

    pain

    Hyperactive and

    nonproductive cough,

    mild to moderate pain

    Pain: intensity, type, location, and

    other characteristics before and 1

    hr after giving product, titrate

    upward by 25% until pain is

    reduced by 1/2 CNS changes:

    dizziness, drowsiness,

    hallucinations, euphoria, LOC, pupil

    rxn B/P, Pulse, Resp:before and

    periodically, if resp < 10/min, dose

    may need to be reduced,

    oversedation may occur Bond

    Status: constipation, provide fluids,

    fiber in diet, may need stimulative

    laxative Allergic Rxn: rash, urticaria

    Cough and Resp.dysfunction:respiratory depression,

    character, rate, rhythm Need for

    pain medication, physical

    dependence, opioid is more

    effective before pain is severe

    Ance

    rosacea/vulgaris,

    Cushing's, measles,

    perioral dermatitis,

    varicella, abrupt

    discontinuation,

    hypersensitivity to

    this product or

    benzyl

    hypersensitivity

    CNS: drowsiness, dizziness,

    light-headedness,

    confusion, H/A, sedation,

    euphoria, dysphoria,

    weakness, hallucinations,

    disorientation, moodchanges, dependence,

    seizures CV: palpitations,

    tachycardia, bradycardia,

    change in B/P,circulatory

    depression, syncope;

    cardiac arrest (children)

    EENT: tinnitus, blurred

    vision, miosis, diplopia GI:

    nausea, vomiting,

    anorexia, constipation,

    cramps, dry mouth, ulcers

    GU: Increased urinary

    output, dysuria, urinary

    retention INTEG: rash,

    urticaria, flushing, pruritus

    RESP: resp depression;

    pulmonary edema,

    bronchopneumonia, resp

    arrest (children)

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Hydrocortisone

    Brands: Cortef

    decreases inflammation by

    suppression of migration of

    polymorphonus clear

    leukocytes, fibroblasts,

    reversal of increased

    capillary permeability, and

    lysosomal stabilization

    Severe inflammation,

    septic shock, adrenal

    insufficiency, ulcerative

    colitis, collagen

    disorders

    1. Potassium, blood glucose, urine

    glucose while on long-term

    therapy; hypokalemia and

    hyperglycemia; potassium

    depletion: paresthesias, fatigue,

    nausea, vomiting, depression,polyuria, dysrhythmias, weakness

    2. B/P every 4hr, pulse; notify

    prescriber if chest pain 3. I&O be

    alert for decreasing urinary output,

    increasing edema, weight daily,

    notify prescriber of weekly gain >5

    lbs 4.Adrenal insufficiency

    (Cushingoid symptoms): nausea,

    anorexia, SOB, moon face, fatigue,

    dizziness, weakness, joint pain

    before and during treatment 5.

    Plasma cortisol levels during long

    term therapy (normal level:138-635

    nmol/L SI units when drawn at 8

    am) 6.Infection:increase temp,

    WBC, even after withdrawal of

    medication; product masks

    infection 7. Mental status: affect

    mood, behavioral changes,

    aggression

    Children < 2yrs,

    psychosis,

    hypersensitivity,

    idiopathic

    thrombocytopenia(I

    M), acute

    glomerulonephritis,

    amebiasis, fungal

    infections, non-

    asthmatic bronchial

    disease, AIDS, TB,

    recent MI

    (associated with left

    ventricular rupture)

    CNS: depression, flushing,

    sweating, H/A, mood

    changes CV: hypertension,

    circulatory collapse,

    thrombophlebitis,

    embolism,tachycardia,

    edema EENT: fungal

    infections, increased

    intraocular pressure,

    blurred vision GI: diarrhea,

    nausea, abdominal

    distention, GI hemorrhage,

    increased appetite,

    pancreatitisHEMA:thrombocytopenia INTEG:

    acne, poor wound healing,

    ecchymosis, petechiae MS:

    fractures, osteoporosis,

    weakness

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Tamoxifen

    Citrate/Nolvadex

    Competes with estrogen for

    binding sites in breast and

    other tissues

    Reduces DNA synthesis and

    estrogen response

    Breast Caner in

    postmenoposal

    women, adjunctively

    with surgery in the

    treatment of breast

    carcinoma with positivelymph nodes

    Assess for an increase in bone or

    tumor pain. Confer with health

    care professional regarding

    analgesics. This transient pain

    usually resolves despite continued

    therapyLab Test Considerations

    Monitor CBC, platelets, and

    calcium levels before and during

    therapy. May cause transient

    hypercalcemia in patients with

    metastases to the bone. An

    estrogen receptor assay should be

    assessed before initiation of

    therapy

    Monitor serum cholesterol and

    triglyceride concentrations in

    patients with pre-existinghyperlipidemia. May cause

    concentrations

    Monitor hepatic function tests

    and thyroxine (T4) periodically

    during therapy. May cause

    serum hepatic enzyme and

    thyroxine concentrations

    Gynecologic examinations

    should be performed regularly;

    may cause variations in

    Papanicolaou and vaginal smearsTop

    Anticoagulant

    therapy including

    coumadin;

    preexisting

    endometrial

    hyperplasia; IM if

    platelets 100

    mg/m2/cycle once every 34 wk

    are rarely used. Differentiate daily

    doses from total dose/cycle.

    Symptoms of high cumulativedoses include muscle cramps

    (localized, painful involuntary

    skeletal muscle contractions of

    sudden onset and short duration)

    and are usually associated with

    advanced stages of peripheral

    neuropathy

    Lab Test Considerations

    Monitor CBC with differential

    and platelet count before and

    routinely throughout therapy. Thenadir of leukopenia,

    thrombocytopenia, and anemia

    occurs within 1823 days and

    recovery 39 days after a dose.

    Withhold further doses until WBC

    is >4000/mm3 and platelet count

    is >100,000/mm3

    Monitor BUN, serum creatinine,

    and CCr before initiation of

    therapy and before each course of

    cisplatin to detect nephrotoxicity.

    May cause BUN and creatinine

    and calcium, magnesium,

    phosphate, sodium, and potassium

    levels that usually occur the 2nd

    wk after a dose. Do not administer

    additional doses until BUN is

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Platinol/Cisplatin cont.

    May cause positive Coombs' test

    result

    Methotrexate/MTX

    Interferes with folic acid

    metabolism. Result is

    inhibition of DNA synthesis

    and cell reproduction (cell-

    cycle S-phasespecific Also

    has immunosuppressive

    activity

    Severe psoriasis, severe

    active rheumatoid

    arthritis, breast cancer,

    lung cancer, certain

    cancers of the headand neck, certain types

    of lymphoma, and

    leukemia

    Monitor CBC and differential priorto and frequently during therapy.

    The nadir of leukopenia and

    thrombocytopenia occurs in 714

    days. Leukocyte and thrombocyte

    counts usually recover 7 days after

    the nadirs. Notify health care

    professional of any sudden drop in

    values

    Monitor renal (BUN and

    creatinine) and hepatic function

    (AST, ALT, bilirubin, and LDH) prior

    to and routinely during therapy.

    Urine pH should be monitored

    prior to high-dose methotrexate

    therapy and every 6 hr during

    leucovorin rescue. Urine pH should

    be kept above 7.0 to prevent renal

    damage

    May cause serum uric acid

    concentrations, especially during

    initial treatment of leukemia and

    lymphoma

    Hypersensitivity

    OB: Lactation:

    Pregnancy or

    lactation

    Pedi: Products

    containing benzyl

    alcohol should not

    be used in neonates

    Use Cautiously in:

    Renal impairment

    (CCr must be B60

    mL/min prior totherapy)

    Patients with

    childbearing

    potential

    Active infections

    bone marrow

    reserve

    Geri: May be more

    sensitive to toxicity

    and adverse events

    CNS: arachnoiditis (IT use

    only), dizziness,

    drowsiness, headache,

    malaise.

    EENT: blurred vision,

    dysarthria transient

    blindness.

    Resp: PULMONARY

    FIBROSIS, intestinal

    pneumonitis.

    GI: anorexia,

    hepatotoxicity, nausea,

    stomatitis, vomiting.

    GU: infertility.

    Derm: alopecia, painfulplaque erosions (during

    psoriasis treatment),

    photosensitivity, pruritus,

    rashes, skin ulceration,

    urticaria.

    Hemat: APLASTIC ANEMIA,

    anemia, leukopenia,

    thrombocytopenia.

    Metabolic: hyperuricemia.

    MS: osteonecrosis, stress

    fracture.Misc: nephropathy, chills,

    fever, soft tissue necrosis.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Vincristine

    Binds to proteins of mitotic

    spindle, causing metaphase

    arrest

    Cell replication is stopped as

    a result (cell cyclespecific

    for M phase)

    Has little or no effect on

    bone marrow

    Hodgkin's disease,Leukemias,

    Neuroblastoma,

    Malignant lymphomas,

    Rhabdomyosarcoma,Wi

    lms' tumor, Other

    tumors

    Monitor blood pressure, pulse,

    and respiratory rate during

    therapy. Report significant

    changes

    Monitor neurologic status. Assess

    for paresthesia (numbness,

    tingling, pain), loss of deep tendonreflexes (Achilles reflex is usually

    first involved), weakness (wrist

    drop or footdrop, gait

    disturbances), cranial nerve palsies

    (jaw pain, hoarseness, ptosis,

    visual changes), autonomic

    dysfunction (ileus, difficulty

    voiding, orthostatic hypotension,

    impaired sweating), and CNS

    dysfunction (decreased level of

    consciousness, agitation,hallucinations). Notify physician if

    these symptoms develop, as they

    may persist for months

    Monitor intake and output ratios

    and daily weight; report significant

    discrepancies. Decreased urine

    output with concurrent

    hyponatremia may indicate SIADH,

    which usually responds to fluid

    restriction

    Assess infusion site frequently

    for redness, irritation, or

    inflammation. If extravasation

    occurs, infusion must be stopped

    and restarted elsewhere to avoid

    damage to subcut tissue. Cellulitis

    and discomfort may be minimized

    by infiltration with hyaluronidase

    and application of moderate heat

    or by application of cold

    compresses

    Assess nutritional status. An

    antiemetic may be used to

    Hypersensitivity

    OB: Lactation:

    Pregnancy or

    lactation

    Use Cautiously in:

    Infection

    bone marrow

    reserve

    Hepatic

    impairment (50%

    dose

    recommended if

    serum bilirubin >3

    mg/dL)

    OB: Instruct

    women of

    childbearing

    potential to avoid

    pregnancy duringtreatment

    CNS: agitation, insomnia,

    mental depression, mental

    status changes.

    EENT: cortical blindness,

    diplopia.

    Resp: bronchospasm.

    GI: nausea, vomiting,

    abdominal cramps,

    anorexia, constipation,

    ileus, stomatitis.

    GU: gonadal suppression,nocturia, oliguria, urinary

    retention.

    Derm: alopecia.

    Endo: syndrome of

    inappropriate antidiuretic

    hormone (SIADH).

    Hemat: anemia,

    leukopenia,

    thrombocytopenia (mild

    and brief).

    Local: phlebitis at IV site,

    tissue necrosis (from

    extravasation).

    Metabolic: hyperuricemia.

    Neuro: ascending

    peripheral neuropathy.

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Vincristine cont.

    minimize nausea and vomiting

    Monitor for symptoms of gout

    (increased uric acid, joint pain,

    edema). Encourage patient to

    drink at least 2 liters of fluid per

    day. Allopurinol or alkalinization

    of urine may be used to decreaseuric acid levels

    Lab Test Considerations

    Monitor CBC prior to and

    periodically throughout therapy.

    May cause slight leukopenia 4

    days after therapy, which resolves

    within 7 days. Platelet count may

    or

    Monitor liver function studies

    (AST, ALT, LDH, bilirubin) and renal

    function studies (BUN, creatinine)prior to and periodically

    throughout therapy

    May cause uric acid. Monitor

    periodically during therapy

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Robaxin

    (Methocarbamol)

    Depresses multisynaptic

    pathways in the spinal cord,

    causing skeletal muscle

    relaxation.

    Adjunct for relief of

    spasm and pain in

    musculoskeletal

    conditions, tetanus.

    Pain, spasm: ROM; Blooddyscrasias: CBC, WBC, differential;

    EEG in epileptic patients;

    Allergic rxns: rash, fever,

    respiratory distress; Severe

    weakness, numbness in

    extremities; Tolerance: increased

    need for medication; CNS

    depression: dizziness, drowsiness.

    Hypersensitivity to

    this product;

    hypersensitivity to

    PEG 300 (inj);

    children

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Decadron

    (Dexamethasone)

    Decreases inflammation by

    suppression of migration of

    polymorphonuclear

    leukocytes, fibroblasts,

    reversal of increased

    capillary permeability and

    lysosomal stabilization.

    Inflammation, allergies,

    neoplasms, cerebral

    edema, septic shock,

    collagen disorders.

    Potassium, blood, urine glucosewhile on long-term therapy;

    hypokalemia and hyperglycemia;

    weight daily: notify MD if weekly

    gain>5lb; B/P q4hr, pulse; notify

    MD of chest pain; I&O ratio: be

    alert for decreasing urinary

    output, increasing edema; plasma

    cortisol levels during long-term

    therapy; infection: fever, WBC

    after withdrawal of medicine;

    potassium depletion; edema,

    hypertension, cardiac symptoms;

    mental status.

    Children

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    Medication

    Brand/GenericMechanism of Action Indications Assessment Contraindications Side Effects

    Valium (Diazepam)

    Potentiates the actions of

    GABA, especially in limbicsystem, reticular formation;

    enhances presympathetic

    inhibition, inhibits spinal

    polysynaptic afferent paths.

    Anxiety, acute alcohol

    withdrawal, adjunct in

    seizure disorders;preoperatively as a

    relaxant, skeletal

    muscle relaxation;

    rectally for acute

    repetitive seizures.

    B/P (lying+standing): if systolic

    drops 20mmHg hold product;

    Pulse; Respiratory rate:

    respirations q5-15min if given IV;

    Blood studies: CBC during long-

    term therapy, blood dyscrasias;

    Hepatic studies: AST, ALT,

    bilirubin, creatinine, LDH, alk phos;

    Degree of anxiety; Pain relief; IV

    site for thrombosis or phlebitis;

    Mental status: mood, sensorium,

    affect, suicidal tendencies;

    Physical dependency; Withdrawal

    symptoms: headache, nausea,

    vomiting, muscle pain.

    Pregnancy (D),

    hypersensitivity to

    benzodiazepines,

    closed-angle

    glaucoma, coma,

    myasthenia gravis,

    ethanol intoxication,

    hepatic disease,

    sleep apnea.

    Dizziness, drowsiness,

    confusion, headache,

    anxiety, tremors,

    depression, insomnia,

    hallucinations, fatigue;

    Orthostatic hypotension,

    ECG changes, tachycardia,

    hypotension; Blurred

    vision, tinnitus, mydriasis;

    constipation, dry mouth,

    NV, diarrhea; Neutropenia;

    Rash, dermatitis, itching;

    Respiratory depression.

    Ancef (Cefazolin)

    Inhibits bacterial cell wall

    synthesis, rendering cell wall

    osmotically unstable, leading

    to cell death; lysis mediated

    by cell wall autolytic

    enzymes.

    Gram-negative bacilli:

    Haemophilus

    influenzae, Escherichia

    coli, Proteus mirabilis,

    Klebsiella; Gram-

    positive organisms:

    Staphylococcus aureus;

    Upper and lower

    respiratory tract,

    urinary tract, skin

    infections, bone, joint,biliary, genital

    infections,

    endocarditis, surgical

    prophylaxis,

    septicemia.

    Sensitivity to penicillin and other

    cephalosporins; Nephrotoxicity:

    increased BUN, creatinine; I&O

    daily; Blood studues:AST, ALT,

    CBC, Hct, bilirubin, LDH, alk phos;

    Electrolytes: K, Na, Cl; Bowel

    pattern daily: Urine output;

    Anaphylaxis; Bleeding:

    ecchymosis, bleeding gums,

    hematuria, stool guaiac daily;Overgrowth of infection:perineal

    itching, malaise, redness, pain,

    swelling, diarrhea, change in

    cough, sputum.

    Hypersensitivity to

    cephalosporins;

    infants

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    N3515 Medications

    Bold and Red life-threatening

    Italics - common

    ATC Anatomical Therapeutic Chemical (ATC) Classification System

    B/P blood pressure

    H/A headache

    LOC loss of consciousness

    N/V nausea & vomiting

    Rxn - reactionResp respiratory/respirations

    SOB- Shortness of Breath

    Abbreviations: N/V: nausea/vomiting. HA: headache. Pt: patient. Mo: month. Incr: increase. Decr: decrease. MI: myocardial infarction. Hx: history. Dx: disease. w/ : with. Wt:

    weight. F&E: fluid & electrolytes.

    aPTT=activated partial thromboplastin time

    AST=aspartate aminotransferase

    ALT=alanine aminotransferase

    BUN=Blood Urea Nitrogen

    CBC=Complete Blood Count

    Hct=Hematocrit

    Hgb=Hemoglobin

    PT=Prothrombin Time

    RA=Rheumatoid Arthritis

    TIA=transient ischemic attack

    MI=Myocardial Infarction

    LFT = Liver Function Test

    HYPERSENSITIVITY REACTIONS, chills, fever, infection, pain, allergic reactions, flu-like syndrome.