Er-Drug Study
Er-Drug Study
Er-Drug Study
Name
Diazepam Valium Antianxiety - Depress the CNS, -Adjunct in the management 10 mg - Monitor BP, PR,RR
agents, probably by of: IM prior to periodically
anticonvulsants, potentiating GABA, 1) Anxiety throughout therapy and
sedative/hyptonics, an inhibitory 2) Preoperative sedation frequently during IV
skeletal muscle neurotransmitter. 3) Conscious sedation therapy.
relaxants (centrally - Produces skeletal - Provides light anesthesia - Assess IV site
acting) muscle relaxation by and anterograde amnesia frequently during
inhibiting spinal - Treatment of status administration,
polysynaptic afferent epilepticus/ uncontrolled diazepam may cause
pathways. seizures phlebitis and venous
- Has anticonvul-sant - Skeletal muscle relaxant thrombosis.
properties due to - Management of the - Prolonged high-dose
enhanced presynaptic symptoms of alcohol therapy may lead to
inhibi- withdrawal psychological or
tion.Therapeutic physical dependence.
effects: Restrict amount of drug
(1) Relief of Anxiety CONTRAINDICATIONS: available to patient.
(2) Sedation - Hypersensitivity Observe depressed
(3) Amnesia - Cross-sensitivity with patients closely for
(4) Skeletal muscle other benzodiazepines may suicidal tendencies.
relaxant occurs - Observe and record
(5) Decreased seizure - Comatose patients intensity, duration and
activity - Pre-existing CNS location of seizure
depression activity. The initial
- Uncontrolled severe dose of diazepam offers
painUse cautiously in: seizure control for 15-
1) Hepatic dysfunction 20 min after
2) Severe renal impairment administration.
3) History of suicide - IM injections are
attempt or drug dependence painful and erratically
absorbed. If IM route is
used, inject deeply into
deltoid muscle for
maximum absorption.
- Caution patient to
avoid taking alcohol or
other CNS depressants
concurrently with this
medication.
- Effectiveness of
therapy can be
demonstrated by
decrease anxiety level;
control of seizures;
decreased
tremulousness.
Generic Name Brand Name Classification Action Indication Dose Nursing
Responsibilities
diphenhydramine Benadryl Antihistamine, Antagonizes the parkinsonism or Tablet: 25, 50 Caution the client that
anticholinergic effect of histamine at drug-induced mg the medication may
antiparkinson H1 receptor sites; extrapyramidal Capsule: 25, 50 cause drowsiness,
agent does not bind or effects, mg creating difficulties or
inactivate histamine, Symptomatic relief Elixir: 12.5 mg/5 hazards or other
Antihistamines of allergies ml activities that require
prevent the Allergic reactions Parenteral: 10, alertness.
physiological actions Anaphylaxis 50 mg/ml vials, • Tell the client to take
of histamine by Acute dystonic prefilled syringe the medication with
preventing reactions Adult: food to decrease GI
histamines from upset.
reaching H1- and The standard • Explain to the client
H2-receptor sites. Contraindications dose of that arising quickly
Antihistamines diphenhydramine form a lying or sitting
provide short-lived Lower respiratory is 25-50 mg, position may cause
benefits and provide diseases such as either IM or IV. orthostatic
only symptomatic astma attacks hypotension.
relief. Antihistamine Patients taking Pediatric: 5 • When taking these
is specific for MAOIs mg/kg/24 hr q 6 medications, the client
conditions in which Hypersensitivity hr PO. 2-5 needs to have blood
histamine excess is Narrow-angle mg/kg IV or IM. cells counts, renal
present (for examle, glaucome function, hepatic
acute urticaria) but is function, and blood
adjunctive therapy in Onset & pressure monitored.
the treatment of Duration • Adverse effects of
anaphylactic shock these drugs occur
because epinephrine Onset: Maximal more commonly in
is more effenctive. effects 1-3 hr elderly clients.
Antihistamines are Duration: 6-12 • Explain to the client
quite specific for hr that use of these drugs
reversing in warm weather may
extrapyramidal increase the likelihood
reactions and are of heatstroke.
probably efficacious
as drying agents in
upper respiratory
and sinus conditions
Generic Name Brand Name Classification Action Indication Dose Nursing Responsibilities
FUROSEMIDE Lasix Rapid-acting potent Treatment of Tablets: • Observe patients
Electrolytic sulfonamide “loop” edema associated 20, 40, receiving parenteral
and water diuretic and with CHF, and drug carefully;
balance antihypertensive with cirrhosis of liver, 80mg. closely monitor BP
agent; pharmacologic effects and kidney Oral and vital signs.
and uses almost disease, including solution: Sudden death from
loop
identical to those of nephrotic 10 cardiac arrest has
diuretic ethacrynic acid. Exact syndrome. May mg/ml, been reported.
mode of action not be used for 40 mg/5 • Monitor BP during
clearly defined; management of ml. periods of diuresis
decreases renal vascular hypertension, Injection: and through period
resistance and may alone or in 10 mg/ml of dosage
increase renal blood combination with adjustment.
flow. other • Observe older adults
antihypertensive closely during period
agents, and for of brisk diuresis.
treatment of Sudden alteration in
hypercalcemia. fluid and electrolyte
Has been used balance may
concomitantly precipitate
with mannitol for significant adverse
treatment of reactions. Report
severe cerebral symptoms to
edema, physician.
particularly in • Lab tests: Obtain
meningitis. frequent blood
count, serum and
urine electrolytes,
CO2, BUN, blood
sugar, and uric acid
values during first
few months of
therapy and
periodically
thereafter.
• Monitor for S&S of
hypokalemia (see
Appendix F).
• Monitor I&O ratio
and pattern. Report
decrease or unusual
increase in output.
Excessive diuresis
can result in
dehydration and
hypovolemia,
circulatory collapse,
and hypotension.
Weigh patient daily
under standard
conditions.
• Monitor urine and
blood glucose &
HbA1C closely in
diabetics and
patients with
decompensated
hepatic cirrhosis.
Drug may cause
hyperglycemia.
• Note: Excessive
dehydration is most
likely to occur in
older adults, those
with chronic cardiac
disease on prolonged
salt restriction, or
those receiving
sympatholytic
agents.
Generic Name Brand Classification Action Indication Dose Nursing
Name Responsibilities
DOPAMINE Dopastat, autonomic nervous Naturally To correct Shock Assessment & Drug
HYDROCHLORIDE Intropin, system agent; occurring hemodynamic Adult/Child: Effects
Revimine alpha- and beta- neurotransmitter imbalance in shock IV 2–5
and immediate syndrome due to MI mcg/kg/min • Monitor blood
adrenergic agonist
precursor of (cardiogenic shock), increased pressure, pulse,
(sympathomimetic norepinephrine. trauma, endotoxic gradually up to peripheral pulses,
) Major septicemia (septic 20–50 and urinary output
cardiovascular shock), open heart mcg/kg/min if at intervals
effects produced surgery, and CHF. necessary prescribed by
by direct action on physician. Precise
alpha- and beta- Contraindication: Renal Failure measurements are
adrenergic Adult: IV 2–5 essential for
receptors and on mcg/kg/min accurate titration
specific Pheochromocytoma of dosage.
dopaminergic ; tachyarrhythmias Dopamine • Report the
receptors in or ventricular Calculation: following
mesenteric and fibrillation. Safe use indicators
renal vascular during pregnancy promptly to
beds. (category C), physician for use
lactation, or Drip Rate= in decreasing or
children is not [(orders) x temporarily
established. (kg) x (drip suspending dose:
set)] / Reduced urine
flow rate in
concentration
absence of
in 1 mL hypotension;
ascending
tachycardia;
Conversion dysrhythmias;
factor: disproportionate
1mg=1000mc rise in diastolic
g pressure (marked
decrease in pulse
1kg=2.2lbs pressure); signs of
peripheral
ischemia (pallor,
cyanosis, mottling,
coldness,
complaints of
tenderness, pain,
numbness, or
burning
sensation).
Monitor
therapeutic
effectiveness. In
addition to
improvement in
vital signs and
urine flow, other
indices of adequate
dosage and
perfusion of vital
organs include loss
of pallor, increase
in toe temperature,
adequacy of nail
bed capillary
filling, and reversal
of confusion or
comatose state.
Advise patient to
report
immediately if
experiencing chest
pa
Generic Brand Classification Action Indication Dose Nursing
Name Name Responsibilities
Mannitol Osmitrol, Diuretic It raises the 1. Acute oliguric renal Adult Assessment – Monitor
Resectisol osmotic failure the following:
pressure of the 2. Toxic overdose Oliguria: 50-100 g as a
plasma 3. Edema 5-25% solution. 1. 1. Vital signs
4. Increased 2. 2. Intake and output
allowing water to intracranial pressure Intracranial/Intraocula 3. 3. Central venous
(ICP) r pressure: 0.25-2 g/kg pressure
be drawn out of
5. Intraocular pressure as 15-25% solution 4. Pulmonary artery
body tissues 6. (IOP) administered for 30-60 pressure
7. Pulmonary minutes. 5. Signs and symptoms
congestion of dehydration (e.g.
Children poor skin turgor, dry
In the oliguric or skin, fever, thirst)
phase of acute oedema; intracranial Oliguria: 0.25-2 g/kg 6. Signs of electrolyte
renal failure, as a 15-20% solution imbalance/deficit
bleeding;
Mannitol for 2-6 hours (e.g. muscular
weakness,
increases CHF; metabolic
Intracranial/Intraocula paresthesia,
osmotic pressure edema with abnormal numbness,
(pressure needed capillary fragility; anuria r pressure: 1-2 g/kg as
a 15-20% solution confusion, tingling
to stop the due to severe renal sensation of
disease; severe administered for 30-60
absorption of minutes. extremity and
dehydration. excessive thirst)
something or
osmosis) of the 7. (for increase ICP)
Neurologic status
glumerular
and intracranial
filtrate, thereby, pressure readings.
promoting 8. (for increase IOP)
diuresis (treating Elevating eye pain
the oliguric phase or decreased visual
of renal failure)
acuity.
and excretes
toxic materials Laboratory Tests
(management for
toxic overdose). 1. Renal function
(BUN and
Creatinine)
It also elevates 2. Serum Electrolyte
blood plasma (Sodium and
osmolality thus, Potassium)
inhibiting the
reabsorption of
Precaution
water and
electrolytes (for
relief of edema) Pregnancy and lactation
and mobilizing (safe use during these
fluids in the conditions is not
cerebral and established)
ocular spaces
(lowers Interventions
intracranial or
intraocular 1. Observe the IV
pressure). site regularly for
infiltration.
2. Administration
rate for oliguria
should be titrated
to produce a urine
output. (about 30-
50 ml/hr in adult
and 2-6 hours in
children)
Generic Brand Name Classification Action Indication Nursing Responsibilities
Name /Dose
Ranitidine Zantac GASTROINTESTIN Completely inhibits •Active Duodenal Ulcer •Instruct patient on
HCL AL AGENT; action of histamine Adults: PO 150mg b.i.d. or proper use of OTC
ANTISECRETORY on the H2 at 300 mg at bedtime. preparation as indicated.
(H2-RECEPTOR receptor sites of Maintenance dose is 150 mg
ANTAGONIST) parietal cells, •Instruct patient on
at bedtime.
decreasing gastric proper use of OTC
IM/IV/Intermittent IV 50 mg preparation as indicated.
acid secretions
every 6 to 8 h.
•Assess patient for
Children 1 mon -16 y/o: PO 2 abdominal pain. Note
to 4 mg/kg twice daily (max, presence of blood in
300 mg/day). emesis, stool, or gastric
aspirate
•Maintenance therapy for
Duodenal and Gastric Ulcers •Ranitidine may be
Adults: 150mg P.O at bedtime added to total parenteral
nutrition solution
Children 1 mon -16 y/o: PO 2
to 4 mg/kg daily up to 150mg •Remind patient to take
once daily prescription
daily
drug at bedtime for best
•Pathologic Hypersecretory results
Conditions •Instruct patient to take
Adults: PO 150 mg twice without regard to meals
daily. Individualize. because absorption isn’t
affected by food
•GERD and Erosive
Esophagitis • Remind patient not to
Adults: PO 150mg b.i.d. confuse ranitidine with
rimantadine: don’t
Children 1 mon -16 y/o: PO 5 confuse Zantac with
to 10 mg/kg daily usually Xanax or Zyrtec
given in 2 divided doses.
•Erosive Esophagitis:
Maintenance dosage is 150mg
P.O. q.i.d.
•Heartburn
Adults and Children 1 mon
-12 y/o and older: 75mg of
Zantac 75 P.O. as symptoms
occur, up to 150mg daily, not
to exceed 2 weeks of
continuous treatment.
CONTRAINDICATION
•Contraindicated in patients
hypersensitive to drug and
those with porphyria
Adverse Reactions:
If Calcium Gluconate
Injections is
administered too
rapidly, nausea,
vomiting, hot
flushes, sweating,
hypotension and
vasomotor collapse,
possibly fatal, may
occur. Soft tissue
calcification due to
extravasation of
calcium solutions
has been reported
Generic Brand Name Classification Action Indication Dose Nursing Responsibilities
Name
Potassium Electrolyte Potassium chloride is Potassium
Chloride used to prevent or to deficiency.
treat low blood levels
of potassium
(hypokalemia). Contraindication:
Potassium levels can Excess of
be low as a result of a potassium ions
disease or from taking produces
certain medicines, or depression of
after a prolonged the heart and
illness with diarrhea may cause
or vomiting. cardiac arrest.
Poisoning may
occur from the
intravenous
injection of even
small doses of
potassium ions
when excretion
is delayed, as in
the presence of
renal
insufficiency.
Adverse
Reactions:
nausea,
vomiting,
diarrhea,
stomach ache,
and flatulence.
hyperphosphatemia
in renal failure:
Adult: suspension
500 mg- 2 2x- 4x a
day
Pharmacodynamics:
Onset: Varies
Peak: Unknown
Duration: 20- 60
minutes (Fasting)
3 hours
( taken 1 hour after
meal)
Generic Name Brand Name Classification Action Indication Dose Nursing Responsibilities
PHENOBARBIT Luminal Sodium central nervous Long-acting barbiturate. Long-term Anticonvulsa Assessment & Drug Effects
AL SODIUM system agent; Sedative and hypnotic management of nt
anticonvulsant; effects of barbiturates tonic-clonic (grand Adult: PO 100–
sedative- appear to be due mal) seizures and 300 mg/d IV/IM • Observe patients
hypnotic; partial seizures; 200–600 mg receiving large doses
barbiturate primarily to interference status epilepticus, closely for at least 30 min to
up to 20
with impulse eclampsia, febrile mg/kg ensure that sedation is not
transmission of cerebral convulsions in Child: PO/IV 3– excessive.
cortex by inhibition of young children. Also 8 mg/kg or • Keep patient under
reticular activating used as a sedative 125 mg/m2/d constant observation when
system. CNS depression in anxiety or tension Neonate: drug is administered IV, and
states; in pediatrics PO/IV 3–4 record vital signs at least
may range from mild
as preoperative and mg/kg/d (max: every hour or more often if
sedation to coma, postoperative 5 mg/kg/d)
depending on dosage, sedation and to indicated.
route of administration, treat pylorospasm Status • Lab tests: Obtain liver
degree of nervous in infants Epilepticus function and hematology
Adult/Child: IV tests and determinations of
system excitability, and
CONTRAINDICATION 15–18 mg/kg serum folate and vitamin D
drug tolerance. Initially, : in single or
barbiturates suppress levels during prolonged
divided doses therapy.
REM sleep, but with Sensitivity to (max: 20
chronic therapy REM barbiturates; mg/kg) • Monitor serum drug
Neonate: IV levels. Serum
sleep returns to normal. manifest hepatic or
15–20 mg/kg concentrations >50 mcg/mL
familial history of may cause coma.
in single or
porphyria; severe Therapeutic serum
divided doses
respiratory or concentrations of 15–40
kidney disease; Sedative mcg/mL produce
history of previous Adult: PO 30– anticonvulsant activity in
120 mg/d IV/IM most patients. These values
addiction to
100–200 mg/d are usually attained after 2
sedative hypnotics; or 3 wk of therapy with a
Child: PO 6
uncontrolled pain; dose of 100–200 mg/d.
mg/kg/d or
pregnancy • Expect barbiturates to
180 mg/m2 in
(particularly early 3 divided produce restlessness when
pregnancy) doses IV/IM given to patients in pain
(category D), 16–100 mg/d because these drugs do not
lactation; sustained (1–3 mg/kg) have analgesic action.
release formulation • Be prepared for
for children <12 y paradoxical responses and
of age. report promptly in older
adult or debilitated patient
and children (i.e., irritability,
marked excitement
[inappropriate tearfulness
and aggression in children],
depression, and confusion).
In conjunction with
local anesthesia,
epinephrine is
contraindicated for
use in finger, toes,
ears, nose, and
genitalia.
In pregnant woman,
drug is
contraindicated.
In breast feeding do
not use the drug or
stop breast feeding.
Name of the Dosage/Route Action/Classificati Indication/ Adverse Effects/ Nursing
Drug on Contraindications Side Effects Responsibilities
Generic Name: 1 mEq/kg IVP, Action: Indications: Adverse Effects: Monitor urinary
may repeat 0.5 pH, calcium,
Sodium mEq/kg 10 min. Neutralizes gastric o Hyperacidity GI: Gastric electrolytes and
Bicarbonate acid o Peptic ulcer distention, phosphate levels.
o Hyperkalemia belching,
o Tricyclic flatulence.
antidepressan
Brand Name: Decrease pepsin t OD Metabolic: Record amount
Arm and Hammer activity o Shock metabolic and consistency of
Pure Baking Soda, associated
alkalosis, stools.
Citrocarbonate, with severe
diarrhea, hypernatremia,
Soda Mint hypokalemia,
Classification: dehydration,
Alkalizing Agent, uncontrolled hyperosmolarity
Clients on low-
Buffer, Antacid, DM (with overdose).
o Reflux sodium diets
electrolyte should evaluate
esophagitis Other: Pain and
irritation at sodium contents of
injection site. antacids.
Contraindications:
Contraindicated in
patients with
metabolic or
respiratory alkalosis;
patients who are
losing chlorides from
vomiting or
continuous GI
suction; patients
taking diuretics
known to produce
hypochloremia
alkalosis; and
patients with
hypocalcemia in
which alkalosis may
produce tetany,
hypertension,
seizures, or heart
failure. Oral sodium
bicarbonate is
contraindicated in
patients with acute
ingestion of strong
mineral acids.
May be repeated
q 5 minutes to
max. of 3 doses.
If the client
doesn’t experience
relief, advise to
seek medical
assistance
immediately.
Hematologic:
To lessen the leukocytosis Avoid OTC
degree of antihistamines.
atrioventricular (A- Other: anaphylaxis
V) heart block when
increased vagal Instruct client not
tone is a major to drive a motor
Side Effects
factor in the vehicle or
conduction defect, CNS: headache, participate in
as in some cases excitement. activities requiring
due to digitalis alertness.
CV: palpitations
Antidote for
cardiovascular
collapse from the
injudicious use of a
cholinergic drug.
Contraindication
Contraindicated in
patients
hypersensitive to
drug and those with
acute angle closure
glaucoma,
obstructive
uropathy,
obstructive disease
of GI tract, paralytic
elius, toxic
magacolon,
intestinal atony,
unstable CV status
in acute
hemorrhage,
asthma, or
myasthenia gravis.
Also contraindicated
in pregnant women.
Name of the Dosage/Route Action/Classificati Indication/ Adverse Effects/ Nursing
Drug on Contraindications Side Effects Responsibilities
LACAMPUINGAN, JOEMAR M.
ADAMSON UNIVERSITY
College of Nursing
BLOCK 403