common medication list - moser
TRANSCRIPT
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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.