EMERGENCY DRUGS: A drug study.

1) AMINOPHYLLINE

Brand Names: Phil Pharmawealth/Atlantic Aminophylline amp Theofil amp
Classification: Antiasthmatic & COPD Preparations
Dosage: Initial: 225-450 mg twice daily, increased if needed. IV Acute severe
bronchospasm. Loading dose: 5 mg/kg (ideal body wt). Maintenance: 0.5 mg/kg/hr. Rate
should not exceed 25 mg/min.
Indication: PO Chronic bronchospasm as hydrate
Action: Increases the level of cAMP resulting in bronchodilation
Adverse Reactions: Nausea, vomiting, abdominal pain, diarrhea, headache, insomnia,
dizziness, anxiety, restlessness; tremor, palpitations. Potentially Fatal: Convulsions, cardiac
arrhythmias, hypotension and sudden death after too rapid IV injection.
Nursing Measures:
Administer to pregnant patients only when clearly neededneonatal tachycardia,
jitteriness, and withdrawal apnea observed when mothers received xanthines up until
delivery.
Caution patient not to chew or crush enteric-coated timed-release forms.
Give immediate-release, liquid dosage forms with food if GI effects occur.
Do not give timed-release forms with food; these should be given on an empty stomach 1
hr before or 2 hr after meals.
Maintain adequate hydration.
Monitor results of serum theophylline levels carefully, and arrange for reduced dosage if
serum levels exceed therapeutic range of 1020 mcg/mL.
Take serum samples to determine peak theophylline concentration drawn 1530 min after
an IV loading dose.
Monitor for clinical signs of adverse effects, particularly if serum theophylline levels are
not available.
Ensure that diazepam is readily available to treat seizures.
Take this drug exactly as prescribed; if a timed-release product is prescribed, take this
drug on an empty stomach, 1 hr before or 2 hr after meals.
Do not to chew or crush timed-release preparations.
Administer rectal solution or suppositories after emptying the rectum.
It may be necessary to take this drug around the clock for adequate control of asthma
attacks.
Avoid excessive intake of coffee, tea, cocoa, cola beverages, chocolate.
Smoking cigarettes or other tobacco products impacts the drug's effectiveness. Try not to
smoke. Notify the care provider if smoking habits change while taking this drug.
Frequent blood tests may be necessary to monitor the effect of this drug and to ensure
safe and effective dosage; keep all appointments for blood tests and other monitoring.
These side effects may occur: Nausea, loss of appetite (taking this drug with food may
help if taking the immediate-release or liquid dosage forms); difficulty sleeping, depression,
emotional lability (reversible).
Report nausea, vomiting, severe GI pain, restlessness, seizures, irregular heartbeat

2) AMIODARONE HYDROCHLORIDE

Brand Names: Anoion tab Cordarone Cordarone inj Sandoz Amiodarone HCl tab
Classification: Cardiac Drugs
Dosage: PO Initial: 200 mg 3 times/day for 1 wk, reduce to 200 mg twice daily for a further
wk. Maintenance: 200 mg/day or lowest effective dose. IV Initial: 5 mg/kg infusion via
central venous catheter. Max: 1.2 g/24 hr.
Indication: Ventricular and supraventricular arrhythmias.
Action: Blocks potassium chloride leading to prolongation of action potential duration.
Adverse Reactions: Blue-grey discoloration of skin, photosensitivity, peripheral neuropathy,
paraesthesia, myopathy, ataxia, tremor, nausea, vomiting, metallic taste, hypothyroidism,
hyperthyroidism, alopecia, sleep disturbances, corneal microdeposits, hot flushes, sweating.
Heart block, bradycardia, sinus arrest, hepatotoxicity, heart failure. Potentially Fatal:
Pulmonary toxicity including pulmonary fibrosis and interstitial pneumonitis, hepatotoxicity,
thyrotoxicity. Ventricular arrhythmias, pulmonary alveolitis, exacerbation of arrhythmias
and rare serious liver injury. Generally in patients with high doses and having preexisting
abnormalities of diffusion capacity.
Nursing Measures:
Monitor cardiac rhythm continuously.
Monitor for an extended period when dosage adjustments are made.
Monitor for safe and effective serum levels (0.52.5 mcg/mL).
Doses of digoxin, quinidine, procainamide, phenytoin, and warfarin may need to be
reduced one-third to one-half when amiodarone is started.
Give drug with meals to decrease GI problems.
Arrange for ophthalmologic exams; reevaluate at any sign of optic neuropathy.
Arrange for periodic chest x-ray to evaluate pulmonary status (every 36 mo).
Arrange for regular periodic blood tests for liver enzymes, thyroid hormone levels.
Drug dosage will be changed in relation to response of arrhythmias; you will need to be
hospitalized during initiation of drug therapy; you will be closely monitored when dosage is
changed.
Have regular medical follow-up, monitoring of cardiac rhythm, chest x-ray, eye exam,
blood tests.
These side effects may occur: Changes in vision (halos, dry eyes, sensitivity to light; wear
sunglasses, monitor light exposure); nausea, vomiting, loss of appetite (take with meals;
eat small, frequent meals); sensitivity to the sun (use a sunscreen or protective clothing
when outdoors); constipation (a laxative may be ordered); tremors, twitching, dizziness,
loss of coordination (do not drive, operate dangerous machinery, or undertake tasks that
require coordination until drug effects stabilize and your body adjusts to it).
Report unusual bleeding or bruising; fever, chills; intolerance to heat or cold; shortness of
breath, difficulty breathing, cough; swelling of ankles or fingers; palpitations; difficulty with
vision.

3) ATROPINE SULFATE

Brand Names: Anespin amp Atropol amp Euro-Med Atropine Sulfate amp Isopto Atropine
eye drops Phil Pharmawealth/Atlantic Atropine amp
Classification: Other Cardiovascular Drugs, Muscle Relaxants, Mydriatic Drugs, Antidotes,
Detoxifying Agents & Drugs Used in Substance Dependence
Indication/Dosage: IV Bradycardia 500 mcg every 3-5 mins. Total: 3 mg. IV/IM
Organophosphorus poisoning 2 mg every 10-30 mins until muscarinic effects disappear or
atropine toxicity appears. IM/SC Premed in anesth 300-600 mcg 30-60 mins before anesth.
IV/IM/SC Overdosage w/ other compd having muscarinic actions 0.6-1 mg, repeat 2 hrly.
Ophth Inflammatory eye disorders As 0.5-1% soln: 1-2 drops 4 times/day. Eye refraction As
1% soln: 1 drop twice daily for 1-2 days before procedure.
Action: An anti-cholinergic that inhibits acetylcholine at the parasympathetic neuroeffector
junction, enhances the conduction of AV node and increases heart rate
Adverse Reactions: Dry mouth, dysphagia, constipation, flushing and dryness of skin,
tachycardia, palpitations, arrhythmias, mydriasis, photophobia, cycloplegia, raised
intraocular pressure. Toxic doses cause tachycardia, hyperpyrexia, restlessness, confusion,
excitement, hallucinations, delirium and may progress to circulatory failure and respiratory
depression. Eye drops: Systemic toxicity especially in children, on prolonged use may lead
to irritation, hyperemia, edema and conjunctivitis. Increased intraocular pressure.
Inhalation: Dryness of mouth, throat. Potentially Fatal: Atrial arrhythmias, AV dissociation,
multiple ventricular ectopics.
Nursing Measures:
Ensure adequate hydration; provide environmental control (temperature) to prevent
hyperpyrexia.
Have patient void before taking medication if urinary retention is a problem.
When used preoperatively or in other acute situations, incorporate teaching about the
drug with teaching about the procedure; the ophthalmic solution is used mainly acutely and
will not be self-administered by the patient; the following apply to oral medication for
outpatients:
Take as prescribed, 30 min before meals; avoid excessive dosage.
Avoid hot environments; you will be heat intolerant, and dangerous reactions may occur.
These side effects may occur: Dizziness, confusion (use caution driving or performing
hazardous tasks); constipation (ensure adequate fluid intake, proper diet); dry mouth (suck
sugarless lozenges; perform frequent mouth care; may be transient); blurred vision,
sensitivity to light (reversible; avoid tasks that require acute vision; wear sunglasses in
bright light); impotence (reversible); difficulty in urination (empty the bladder prior to
taking drug).
Report rash; flushing; eye pain; difficulty breathing; tremors, loss of coordination;
irregular heartbeat, palpitations; headache; abdominal distention; hallucinations; severe or
persistent dry mouth; difficulty swallowing; difficulty in urination; constipation; sensitivity to
light.

4) BUMETANIDE

Brand Names: Burinex amp Burinex tab
Classification: Sulfonamide Diuretics
Indication/Dosage: PO edema 1 mg once daily, 2nd dose 6-8 hr later if needed. Refractory
edema Initial: 5 mg/day, may increase dose depending on response. Max: 10 mg/day. HTN
0.5-1 mg/day. Max: 5 mg/day. IV Pulmonary edema 1-2 mg, repeat 20 mins. later if
needed. IV/IM Emergency edema 0.5-1 mg, then adjust according to response.
Action: inhibits Sodium and Chloride reabsorption at the ascending loop of Henle
Adverse Reactions: Muscle cramps, dizziness, hypotension, headache, nausea, impaired
hearing, pruritus, ECG changes, musculoskeletal pain, rash, chest discomfort, renal failure,
premature ejaculation, thrombocytopenia, hypokalemia, hypomagnesaemia, hyponatremia,
hyperuricemia, hyperglycemia, hypocalcaemia.
Nursing Measures:
Give with food or milk to prevent GI upset.
Mark calendars or use reminders if intermittent therapy is best for treating edema.
Give single dose early in day so increased urination will not disturb sleep.
Avoid IV use if oral use is possible.
Arrange to monitor serum electrolytes, hydration, liver function during long-term therapy.
Provide diet rich in potassium or supplemental potassium.
Record alternate day or intermittent therapy on a calendar or dated envelopes.
Take the drug early in day so increased urination will not disturb sleep; take with food or
meals to prevent GI upset.
Weigh yourself on a regular basis, at the same time, and in the same clothing; record the
weight on your calendar.
These side effects may occur: Increased volume and frequency of urination; dizziness,
feeling faint on arising, drowsiness (avoid rapid position changes; hazardous activities, such
as driving; and alcohol consumption); sensitivity to sunlight (use sunglasses, sunscreen,
wear protective clothing); increased thirst (suck sugarless lozenges; use frequent mouth
care); loss of body potassium (a potassium-rich diet, or supplement will be needed).
Report weight change of more than 3 lb in 1 day; swelling in ankles or fingers; unusual
bleeding or bruising; nausea, dizziness, trembling, numbness, fatigue; muscle weakness or
cramps.

5) CALCIUM GLUCONATE

Brand Names: Phil Pharmawealth/Harson Calcium Gluconate amp
Classification: Electrolytes
Indication/Dosage: PO Hypocalcaemia 10-50 mmol/day. IV Hypocalcaemic tetany 2.25
mmol via slow inj , then 58-77 mL of 10% soln diluted and administered as a continuous IV
infusion. Antidote in severe hypermagnesaemia; Severe hyperkalaemia 10 mL of 10% soln,
repeat every 10 mins if needed.
Action: replaces Calcium and maintains Calcium level
Adverse Reactions: GI irritation; soft-tissue calcification, skin sloughing or necrosis after
IM/SC inj. Hypercalcaemia characterised by anorexia, nausea, vomiting, constipation,
abdominal pain, muscle weakness, mental disturbances, polydipsia, polyuria,
nephrocalcinosis, renal calculi; chalky taste, hot flushes and peripheral vasodilation.
Potentially Fatal: Cardiac arrhythmias and coma.
Nursing Measures:
Make sure prescriber specifies form of calcium to be given; crash carts may contain both
calcium gluconate and calcium chloride.
Tell patient to take oral calcium 1 to 11/2 hours after meals if GI upset occurs.
Give I.M. injection in gluteal region in adults and in lateral thigh in infants. Use I.M. route
only in emergencies when no I.V. route is available bec. of irritation of tissue by calcium
salts.
Tell patient to take oral calcium with a full glass of water.
Monitor calcium levels frequently. Hypercalcemia may result after large doses in chronic
renal failure. Report abnormalities.

6) CAPTOPRIL

Brand Names: Ace-Bloc tab Capomed tab Capotec tab Capoten tab Captor tab Captril tab
Cardiovaz tab Conamid tab Hartylox tab Normil tab Phil Pharmawealth/Panion & BF
Captopril tab Prelat tab Primace tab Retensin tab Spec-Ace tab Tensoril tab Unihype tab
Vasostad tab
Classification: ACE Inhibitors
Indication/Dosage: PO HTN Initial: 12.5 mg twice daily. Maintenance: 25-50 mg twice daily.
Max: 50 mg 3 times/day. Heart failure Initial: 6.25-12.5 mg 2-3 times/day. Max: 50 mg 3
times/day. Post MI Start 3 days after MI. Initial: 6.25 mg/day, may increase after several
wk to 150 mg/day in divided doses if needed and tolerated. HTN in diabetic nephropathy
75-100 mg/day in divided doses.
Action: inhibits ACE, reduces Sodium and water retention, lowers blood pressure
Adverse Reactions: Hypotension, tachycardia, chest pain, palpitations, pruritus,
hyperkalaemia. Proteinuria; angioedema, skin rashes; taste disturbance, nonproductive
cough, headache. Potentially Fatal: Neutropenia, usually occurs within 3 mth of starting
therapy especially in patients with renal dysfunction or collagen diseases. Hyperkalaemia.
Anaphylactic reactions.
Nursing Measures:
Administer 1 hr before or 2 hr after meals.
Alert surgeon and mark patient's chart with notice that captopril is being taken; the
angiotensin II formation subsequent to compensatory renin release during surgery will be
blocked; hypotension may be reversed with volume expansion.
Monitor patient closely for fall in BP secondary to reduction in fluid volume (excessive
perspiration and dehydration, vomiting, diarrhea); excessive hypotension may occur.
Reduce dosage in patients with impaired renal function.
Take drug 1 hr before or 2 hr after meals; do not take with food. Do not stop without
consulting your health care provider.
Be careful of drop in blood pressure (occurs most often with diarrhea, sweating, vomiting,
dehydration); if light-headedness or dizziness occurs, consult your health care provider.
Avoid over-the-counter medications, especially cough, cold, allergy medications that may
contain ingredients that will interact with ACE inhibitors. Consult your health care provider.
These side effects may occur: GI upset, loss of appetite, change in taste perception
(limited effects, will pass); mouth sores (perform frequent mouth care); rash; fast heart
rate; dizziness, light-headedness (usually passes after the first few days; change position
slowly, and limit your activities to those that do not require alertness and precision).
Report mouth sores; sore throat, fever, chills; swelling of the hands, feet; irregular
heartbeat, chest pains; swelling of the face, eyes, lips, tongue, difficulty breathing.

7) CLONIDINE

Brand Names: Catapin amp Catapres amp Catapres tab
Classification: Other Antihypertensives
Indication/Dosage: PO HTN Initial: 50-100 mcg 3 times/day. Max: 2,400 mcg/day.
Menopausal flushing; Migraine prophylaxis 50 mcg twice daily, up to 75 mg twice daily. IV
Hypertensive crisis 150-300 mcg via slow inj. Max: 750 mcg over 24 hr. Epidural Severe
cancer pain Initial: 30 mcg/hr as continuous infusion in combination w/ an opioid.
Transdermal HTN As patch releasing 100-300 mcg clonidine base/day at constant rate:
Apply once wkly.
Action: stimulates alpha 2 receptors and inhibits central vasomotor centers, lowers
peripheral vascular resistance, blood pressure, and heart rate
Adverse Reactions: Dry mouth, drowsiness, dizziness, headache, constipation, impotence,
vivid dreams, urinary retention; dry, itching, burning sensation in the eye; fluid or
electrolyte imbalance, GI upset, paralytic ileus, orthostatic hypotension, weakness,
sedation, pruritus, myalgia, urticaria, nausea, insomnia, arrhythmias, agitation. Reduced GI
motility at times may cause paralytic ileus. Potentially Fatal: Transient hypertension or
profound hypotension, respiratory depression, convulsion. Clonidine withdrawal syndrome
could be life threatening. Bradycardia, coma and disturbances in conduction (in individuals
with preexisting diseases of SA/AV nodes, overdose or on digitalis).
Nursing Measures:
Take drug 1 hr before or 2 hr after meals; do not take with food. Do not stop without
consulting your health care provider.
Be careful of drop in blood pressure (occurs most often with diarrhea, sweating, vomiting,
dehydration); if light-headedness or dizziness occurs, consult your health care provider.
Avoid over-the-counter medications, especially cough, cold, allergy medications that may
contain ingredients that will interact with ACE inhibitors. Consult your health care provider.
These side effects may occur: GI upset, loss of appetite, change in taste perception
(limited effects, will pass); mouth sores (perform frequent mouth care); rash; fast heart
rate; dizziness, light-headedness (usually passes after the first few days; change position
slowly, and limit your activities to those that do not require alertness and precision).
Report mouth sores; sore throat, fever, chills; swelling of the hands, feet; irregular
heartbeat, chest pains; swelling of the face, eyes, lips, tongue, difficulty breathing.
Take this drug exactly as prescribed. Do not miss doses. Do not discontinue the drug
unless so instructed. Do not discontinue abruptly; life-threatening adverse effects may
occur. If you travel, take an adequate supply of drug.
Use the transdermal system as prescribed; refer to directions in package insert, or contact
your health care provider with questions. Be sure to remove old systems before applying
new ones.
Attempt lifestyle changes that will reduce your BP: stop smoking and using alcohol; lose
weight; restrict intake of sodium (salt); exercise regularly.
Use caution with alcohol. Your sensitivity may increase while using this drug.
These side effects may occur: Drowsiness, dizziness, light-headedness, headache,
weakness (often transient; observe caution driving or performing other tasks that require
alertness or physical dexterity); dry mouth (suck on sugarless lozenges or ice chips); GI
upset (eat small, frequent meals); dreams, nightmares (reversible); dizziness, light-
headedness when you change position (get up slowly; use caution climbing stairs);
impotence, other sexual dysfunction, decreased libido (discuss with care providers); breast
enlargement, sore breasts; palpitations.
Report urinary retention, changes in vision, blanching of fingers, rash.

8) DIAZEPAM

Brand name: Valium
Classification: Anxiolytics
Dosage: 10mg/2ml
Indication: relief of anxiety, agitation & tension due to psychoneurotic states & transient
situational disturbances
Action: a benzodiazepine that probably potentiates the effects of GABA, depresses the CNS
& suppresses the spread of seizure activity
Adverse Reaction: drowsiness,dysarthria, slurred speech, tremor, transient amnesia,
fatigue, ataxia, headache, insomnia, paradoxical anxiety, hallucination
Nursing Measures:
Do not administer intra-arterially; may produce arteriospasm, gangrene.
Change from IV therapy to oral therapy as soon as possible.
Do not use small veins (dorsum of hand or wrist) for IV injection.
Reduce dose of narcotic analgesics with IV diazepam; dose should be reduced by at least
one-third or eliminated.
Carefully monitor P, BP, respiration during IV administration.
Maintain patients receiving parenteral benzodiazepines in bed for 3 hr; do not permit
ambulatory patients to operate a vehicle following an injection.
Monitor EEG in patients treated for status epilepticus; seizures may recur after initial
control, presumably because of short duration of drug effect.
Monitor liver and kidney function, CBC during long-term therapy.
Taper dosage gradually after long-term therapy, especially in epileptic patients.
Arrange for epileptic patients to wear medical alert ID indicating that they are epileptics
taking this medication.
Discuss risk of fetal abnormalities with patients desiring to become pregnant.

9) DIGOXIN

Brand name: Digitek, Lanoxicaps, Lanoxin, Novo-Digoxin (CAN)
Classification: Inotropics
Dosage: 5mg/2ml
Indication: Cardiac failure accompanied by atrial fibrillation; management of chronic cardiac
failure where systolic dysfunction or ventricular dilatation is dominant; management of
certain supraventricular arrhythmias, particularly chronic atrial flutter & fibrillation.
Action: inhibits sodium-potassium activated adenosine triphosphate, promoting movement
of calcium from extracellular to intra-cytoplasm and strengthening myocardial contraction,
also acts on CNS to enhance vagal tone
Adverse Reaction: nausea, vomiting, anorexia, headache, facial pain, fatigue, weakness,
dizziness, drowsiness, disorientation, mental confusion, bad dreams, convulsions
Nursing Measures:
Monitor apical pulse for 1 min before administering; hold dose if pulse < 60 in adult or <
90 in infant; retake pulse in 1 hr. If adult pulse remains < 60 or infant < 90, hold drug and
notify prescriber. Note any change from baseline rhythm or rate.
Check dosage and preparation carefully.
Avoid IM injections, which may be very painful.
Follow diluting instructions carefully, and use diluted solution promptly.
Avoid giving with meals; this will delay absorption.
Have emergency equipment ready; have K+ salts, lidocaine, phenytoin, atropine, cardiac
monitor on standby in case toxicity develops.
Monitor for therapeutic drug levels: 0.52 ng/mL.

10) DIPENHYDRAMINE

Brand name: Benadryl
Classification: antihistamine
Dosage: 50mg/ml
Indication: Hay fever, urticaria, vasomotor rhinitis, angioneurotic edema, drug sensitization,
serum & penicillin reaction, contact dermatitis, atopic eczema, other allergic dermatoses,
pruritus, food sensitivity, parkinsonism, motion sickness.
Action: prevents histamine mediated responses, drug provides local anesthesia and
suppresses cough reflex
Adverse Reaction: CV and CNS effects, blood disorders, GI disturbances, anti-muscarinic
effects and allergic reactions.
Nursing Measures:
Monitor carefully, assess for confusion, delirium, other anticholinergic side effects and fall
risk. Institute measures to prevent falls.
Assess movement disorder before and after administration.
Caution patient not to use oral OTC diphenhydramine products with any other product
containing diphenhydramine, including products used topically.
It can cause excitation in children. Caution parents or caregivers about proper dose
calculation; overdosage, especially in infants and children, can cause hallucinations,
seizures or death Inform patient that this drug may cause dry mouth. Frequent oral rinses,
good oral hygiene, and sugarless gum or candy may minimize this effect. Notify dentist if
dry mouth persists for more than 2 weeks.

11) EPINEPHRINE

Brand name:
Epinephrine Bitartrate
Aerosols: Primatene Mist
Epinephrine Borate
Ophthalmic solution: Epinal
Epinephrine Hydrochloride
Injection, OTC nasal solution: Adrenalin Chloride
Ophthalmic solution: Epifrin, Glaucon
Insect sting emergencies: EpiPen Auto-Injector (delivers 0.3 mg IM adult dose), EpiPen Jr.
Auto-Injector (delivers 0.15 mg IM for children)
OTC solutions for nebulization: AsthmaNefrin, microNefrin, Nephron, S2
Classification: Sympathomimetic, Alpha-adrenergic agonist, Beta1and beta2-adrenergic
agonist, Cardiac stimulant, Vasopressor, Bronchodilator, Antasthmatic drug, Nasal
decongestant, Mydriatic, Antiglaucoma drug
Dosage: 1mg/ml
Indication: Acute asthmatic attacks, Advanced cardiac life support
Action: Naturally occurring neurotransmitter, the effects of which are mediated by alpha or
beta receptors in target organs. Effects on alpha receptors include vasoconstriction,
contraction of dilator muscles of iris. Effects on beta receptors include positive chronotropic
and inotropic effects on the heart (beta1 receptors); bronchodilation, vasodilation, and
uterine relaxation (beta2 receptors); decreased production of aqueous humor.
Adverse Reaction: drowsiness, headache, nervousness, tremors, cerebral hemorrhage,
dizziness, weakness, vertigo, pain
Nursing Measures:
Monitor heart rate.
Use extreme caution when calculating and preparing doses; epinephrine is a very potent
drug; small errors in dosage can cause serious adverse effects. Double-check pediatric
dosage.
Use minimal doses for minimal periods of time; "epinephrine-fastness" (a form of drug
tolerance) can occur with prolonged use.
Protect drug solutions from light, extreme heat, and freezing; do not use pink or brown
solutions. Drug solutions should be clear and colorless (does not apply to suspension for
injection).
Shake the suspension for injection well before withdrawing the dose.
Rotate SC injection sites to prevent necrosis; monitor injection sites frequently.
Keep a rapidly acting alpha-adrenergic blocker (phentolamine) or a vasodilator (a nitrate)
readily available in case of excessive hypertensive reaction.
Have an alpha-adrenergic blocker or facilities for intermittent positive pressure breathing
readily available in case pulmonary edema occurs.
Keep a beta-adrenergic blocker (propranolol; a cardioselective beta-blocker, such as
atenolol, should be used in patients with respiratory distress) readily available in case
cardiac arrhythmias occur.
Do not exceed recommended dosage of inhalation products; administer pressurized
inhalation drug forms during second half of inspiration, because the airways are open wider
and the aerosol distribution is more extensive. If a second inhalation is needed, administer
at peak effect of previous dose, 35 min.
Use topical nasal solutions only for acute states; do not use for longer than 35 days, and
do not exceed recommended dosage. Rebound nasal congestion can occur after
vasoconstriction subsides.
Do not exceed recommended dosage; adverse effects or loss of effectiveness may result.
Read the instructions that come with respiratory inhalant products, and consult your health
care provider or pharmacist if you have any questions.
To give eye drops: Lie down or tilt head backward, and look up. Hold dropper above eye;
drop medicine inside lower lid while looking up. Do not touch dropper to eye, fingers, or any
surface. Release lower lid; keep eye open, and do not blink for at least 30 sec. Apply gentle
pressure with fingers to inside corner of the eye for about 1 min; wait at least 5 min before
using other eye drops.
These side effects may occur: Dizziness, drowsiness, fatigue, apprehension (use caution if
driving or performing tasks that require alertness); anxiety, emotional changes; nausea,
vomiting, change in taste (eat frequent small meals); fast heart rate. Nasal solution may
cause burning or stinging when first used (transient). Ophthalmic solution may cause slight
stinging when first used (transient); headache or brow ache (only during the first few days).
Report chest pain, dizziness, insomnia, weakness, tremor or irregular heart beat
(respiratory inhalant, nasal solution), difficulty breathing, productive cough, failure to
respond to usual dosage (respiratory inhalant), decrease in visual acuity (ophthalmic).

12) FUROSEMIDE

Brand name: Apo-Furosemide (CAN), Furoside (CAN), Lasix, Myrosemide (CAN)
Classification: loop diuretics
Dosage: 20mg/2ml
Indication: edema, hypertension
Action: inhibits Sodium and Chloride reabsorption at the proximal and distal tubules and the
ascending loop of Henle
Adverse Reaction: vertigo, headache, dizziness, paresthesia, weakness, restlessness, fever,
nocturia, oliguria, polyguria
Nursing Measures:
Monitor BP after administration
Administer with food or milk to prevent GI upset.
Reduce dosage if given with other antihypertensives; readjust dosage gradually as BP
responds.
Give early in the day so that increased urination will not disturb sleep.
Avoid IV use if oral use is at all possible.
Do not mix parenteral solution with highly acidic solutions with pH below 3.5.
Do not expose to light, may discolor tablets or solution; do not use discolored drug or
solutions.
Discard diluted solution after 24 hr.
Refrigerate oral solution.
Measure and record weight to monitor fluid changes.
Arrange to monitor serum electrolytes, hydration, liver function.
Arrange for potassium-rich diet or supplemental potassium as needed.

13) HYDRALAZINE HYDROCHLORIDE

Brand name: Supres
Classification: antihypertension
Dosage: 20mg/ml
Indication: For hypertensive patient
Action: a direct acting peripheral vasodilator that relaxes arteriolar smooth muscles
Adverse Reaction: tachycardia, palpitation, angina pectoris, severe headache, dizziness,
weight gain, GI disturbances, pruritus, rashes, nausea and vomiting
Nursing Measures:
Give oral drug with food to increase bioavailability(drug should be given in a consistent
relationship ti ingestion of food for consistent response to therapy).
Drug may cause a syndrome resembling systemic lupus erythematosus (SLE). Arrange for
CBC, LE cell preparations, and ANA titers before and periodically during prolonged therapy,
even in the asymptomatic patient. Discontinue if blood dyscrasias occur. Reevaluate therapy
if ANA or LE tests are positive.
Arrange for pyridoxine if patient develops symptoms of peripheral neuritis.
Monitor patient for orthostatic hypotension which is most marked in the morning and in
hot weather, and with alcohol or exercise.

14) HYDROCORTISONE SODIUM SUCCINATE

Brand name: A-hydroCort, Solu-Cortef
Classification: corticosteroid hormones
Stock Dose:100 mg/ 2 mL, 250 mg/ 2 mL
Indication: endocrine, hematologic, rheumatic & collagen disorders, dermatologic, ophth,
GI, resp & neoplastic diseases, edematous states, control of severe incapacitating allergic
conditions, TB meningitis w/ subarachnoid block or impending block when used concurrently
with appropriate anti-TB chemotherapy, shock secondary to adrenocortical insufficiency or
shock unresponsive to conventional therapy when adrenocortical insufficiency may be
present
Action: Decreases inflammation, mainly by stabilizing leukocyte lysosomal membranes,
suppresses immune response, stimulates bone marrow and influences protein, fat, and
carbohydrate metabolism
Adverse Reactions: fluid and electrolyte disturbances, decreased carbohydrate tolerance,
impaired wound healing, thin fragile skin, muscle weakness, steroid myopathy,
osteoporosis, aseptic necrosis, peptic ulceration w/ possible perforation, cataracts, increased
intraocular and intracranial pressure, growth retardation, Cushingoid state, protein
catabolism, psychic derangements, exophthalmos, masking of infections, gasping
syndrome, seizures, menstrual irregularities.
Nursing Measures:
Give daily before 9 AM to mimic normal peak diurnal corticosteroid levels and minimize
HPA suppression.
Space multiple doses evenly throughout the day.
Do not give IM injections if patient has thrombocytopenic purpura.
Rotate sites of IM repository injections to avoid local atrophy.
Use minimal doses for minimal duration to minimize adverse effects.
Taper doses when discontinuing high-dose or long-term therapy.
Arrange for increased dosage when patient is subject to unusual stress.
Use alternate-day maintenance therapy with short-acting corticosteroids whenever
possible.
Do not give live virus vaccines with immunosuppressive doses of hydrocortisone.
Provide antacids between meals to help avoid peptic ulcer.

15) ISOSORBIDE-5- MONONITRATE

Brand name: Imdur
Classification: anti- anginal drug
Stock Dose: SL: 5 mg/mL ; Oral: 30 mg, 60 mg
Indication: prophylactic treatment of angina pectoris
Action: Thought to reduce cardiac oxygen demand by decreasing preload and afterload.
Drug also may increase blood flow through the collateral coronary vessels
Adverse Reactions: headache, hypotension w/ dizziness and nausea, tachycardia
Nursing Measures:
Monitor BP and heart rate.
Assess location, duration, intensity, and precipitating factors of anginal pain.

16) ISOSORBIDE DINITRATE
Brand name: Isoket IV
Classification: anti anginal drug
Stock: IV amp 10 mg/ 10 mL
Dose: 10 mg/10mL
Indication: unresponsive left ventricular failure secondary to acute MI, severe or unstable
angina pectoris
Action: Isosorbide dinitrate is a smooth muscle relaxant. It is particularly effective on
vascular and bronchial smooth muscle. Its systemic cardiovascular effects are mainly due to
a decrease in venous return (pooling of blood in the peripheral venous system).
Consequently, ventricular end-diastolic pressure and volume are diminished, thus reducing
cardiac work and implicitly myocardial oxygen requirements. The arterial vessels are dilated
as well, though to a lesser degree. This results in a slight drop in aortic and systemic blood
pressure relieving the myocardium from a part of its afterload. These nitrate-induced
changes account for both the antianginal effects of isosorbide dinitrate and for its beneficial
effects in the treatment of congestive heart failure.
Side effects/ adverse reactions: severe cerebral flow deficiency and decreased coronary
perfusion may develop, nitrate headache and nausea.
Nursing Measures:
Monitor BP and heart rate.
Assess location, duration, intensity, and precipitating factors of anginal pain.

17) MAGNESIUM SULFATE

Brand name: Elin Magnesium Sulfate
Classification: anticonvulsant
Dosage: 250 mg/10 mL
Indication: treatment of hypomagnesemia accompanied by signs of tetany, control of HTN,
encephalophathy & convulsions, prevention & control of convulsions in patients w/
preeclampsia or eclampsia, prevention of hypomagnesemia in patients receiving TPN
Action: may decrease acetylcholine released by nerve impulses, but its anticonvulsant
mechanism is unknown
Adverse Reactions: flushing, sweating, hypotension, muscular weakness, sedation &
confusion; decreased deep tendon reflexes; resp. paralysis
Nursing Measures:
Monitor the following: I.V.: Rapid administration: ECG monitoring, vital signs, deep tendon
reflexes; magnesium, calcium, and potassium levels; renal function during administration.
Obstetrics: Patient status including vital signs, oxygen saturation, deep tendon reflexes,
level of consciousness, fetal heart rate, maternal uterine activity. Oral: Renal function;
magnesium levels; bowel movements.

18) MEPERIDINE HYDROCHLORIDE

Brand name: Demerol
Classification: antivertigo drug
Dosage: 100 mg/ 2mL
Indication: relief of moderate to severe pain, pre-op medication, support of anesth & obstet
analgesia
Action: binds with opiate receptors in the CNS, altering perception of and emotional
response to pain
Adverse Reactions: resp. depression, circulatory depression, resp arrest, shock, cardiac
arrest, GI disturbance, light headedness, dizziness, sedation, nausea, vomiting, sweating,
euphoria, dysphoria, weakness, headache, tremor, agitation, uncoordinated muscle
movements, severe convulsions, transient hallucinations & disorientation, visual
disturbance, flushing, tachycardia, bradycardia, palpitation, hypotension, syncope, phlebitis,
urinary retention, allergic reactions, pain at injection site and local tissue irritation.
Nursing Measures:
Make position changes slowly and in stages particularly from recumbent to upright
posture. Lie down immediately if light-headedness or dizziness occurs.
Lie down when feeling nauseated and to notify physician if this symptom persists. Nausea
appears to worsen with ambulation.
Avoid driving and other potentially hazardous activities until reaction to drug is known.
Codeine may impair ability to perform tasks requiring mental alertness and therefore to.
Do not take alcohol or other CNS depressants unless approved by physician.
Hyperactive cough may be lessened by avoiding irritants such as smoking, dust, fumes
and other air pollutants. Humidification of ambient air may provide some relief.
Do not breast feed while taking this drug.

19) METOCLOPRAMIDE

Brand name: Apo-Metoclop (CAN), Maxeran (CAN), Maxolon, Nu-Metoclopramide (CAN),
Octamide PFS, Reglan
Classification: antiemetic & anti-spasmodic
Dosage: 10 mg/ 2mL
Indication: disturbances of GI motility, nausea & vomiting of central & peripheral origin
associated w/ surgery, metabolic diseases, infectious & drug induced diseases, facilitate
small bowel intubation & radiological procedures of GIT
Action: stimulates motility of upper GI tract, increases lower esophageal sphincter tone, and
blocks dopamine receptors at the chemoreceptor trigger zone
Adverse Reactions: extrapyramidal reactions, drowsiness, fatigue & lassitude, anxiety, less
frequently, insomnia, headache, dizziness, nausea, galactorrhea, gynecomastia, bowel
disturbances.
Nursing Measures:
Monitor BP carefully during IV administration.
Monitor for extrapyramidal reactions, and consult physician if they occur.
Monitor diabetic patients, arrange for alteration in insulin dose or timing if diabetic control
is compromised by alterations in timing of food absorption.
Keep diphenhydramine injection readily available in case extrapyramidal reactions occur
(50 mg IM).
Have phentolamine readily available in case of hypertensive crisis (most likely to occur
with undiagnosed pheochromocytoma).

20) MIDAZOLAM HYDROCHLORIDE

Brand name: Dormicum
Classification: hypnotics & sedatives
Dosage: 5mg/5mL
Indication: tab: disturbances of sleep rhythm, insomnia esp difficulty in falling asleep either
initially or after premature awakening, tab/inj: sedation in premed before surgical or
diagnostic procedures, induction & maintenance of anesth.
Action: may potentiate the effects of GABA, depress the CNS, and suppress the spread of
seizure activity
Adverse Reactions: rarely cardioresp adverse events, nausea, vomiting, headache,
hiccoughs, laryngospasm, dyspnoea, hallucination, oversedation, drowsiness, ataxia, rash,
paradoxical reactions, amnesic episodes.
Nursing Measures:
Do not administer intra-arterially, which may produce arteriospasm or gangrene.
Do not use small veins (dorsum of hand or wrist) for IV injection.
Administer IM injections deep into muscle.
Monitor IV injection site for extravasation.
Arrange to reduce dose of midazolam if patient is also being given opioid analgesics;
reduce dosage by at least 50% and monitor patient closely.
Monitor level of consciousness prior to, during, and for at least 26 hr after administration
of midazolam.
Carefully monitor P, BP, and respirations carefully during administration.
Keep resuscitative facilities readily available; have flumazenil available as antidote if
overdose should occur.
Keep patients in bed for 3 hr; do not permit ambulatory patients to operate a vehicle
following an injection.
Arrange to monitor liver and kidney function and CBC at intervals during long-term
therapy.
Establish safety precautions if CNS changes occur (use side rails, accompany ambulating
patient).
Provide comfort measures and reassurance for patients receiving diazepam for tetanus.
Arrange to taper dosage gradually after long-term therapy.
Provide patient with written information regarding recovery and follow-up care. Midazolam
is a potent amnesiac and memory may be altered.

21) MORPHINE SULFATE

Brand name: Morin
Classification: Analgesics (Opioid)
Dosage: Adult 5-20 mg IM/SC 4 hrly. Severe or chronic pain Childn 10 mg IM/SC 4 hrly,
range: 5-20 mg; 6-12 yr 5-10 mg, 1-5 yr 2.5-5 mg, 1-12 mth 200 mcg/kg, <1 mth 150
mcg/kg 4 hrly. Max: 15 mg. Analgesic effect Ped 100-200 mcg/kg SC 4 hrly, max: 15
mg/dose; or 50-100 mcg/kg slow IV. Pre-op 50-100 mcg/kg IM, max: 10 mg/dose.
Indication: Relief of moderate to severe pain not responsive to non-narcotic analgesics.
Premed. Analgesic adjunct in general anesth esp in pain associated w/ cancer, MI & surgery.
Alleviates anxiety associated w/ severe pain. Hypnotic for pain-related sleeplessness.
Action: alters perception and emotional response to pain
Adverse Reactions: Lightheadedness, dizziness, sedation, nausea, vomiting, constipation &
sweating.
Nursing Measures:
Caution patient not to chew or crush controlled-release preparations.
Dilute and administer slowly IV to minimize likelihood of adverse effects.
Tell patient to lie down during IV administration.
Keep opioid antagonist and facilities for assisted or controlled respiration readily available
during IV administration.
Use caution when injecting SC or IM into chilled areas or in patients with hypotension or in
shock; impaired perfusion may delay absorption; with repeated doses, an excessive amount
may be absorbed when circulation is restored.
Reassure patients that they are unlikely to become addicted; most patients who receive
opioids for medical reasons do not develop dependence syndromes.

22) NICARDIPINE HYDROCHLORIDE

Brand name: Cardepine
Classification: Calcium Antagonists
Dosage: IV infusion Dilute to 10-20 mg/100 mL (conc of 1.01-0.02%). Initial infusion rate:
5 mg/hr; titrate dose up to 15 mg/hr until desired therapeutic response is achieved (DBP
<95 mmHg, SBP <140 mmHg). Maintenance rate: Can be tapered down to 10 mg/hr. IV
bolus inj 2-7 mg w/out dilution given over 1-2 min.
Indication: Hypertensive emergencies or urgencies, peri-op & post-op HTN, hypertensive
states of NPO patients.
Action: a Calcium channel blocker that inhibits Calcium ion influx across cardiac and smooth
muscle cells, also dilates coronary arteries and arterioles
Adverse Reactions: Peripheral edema, headache, tachycardia, palpitations, localized
thrombophlebitis & hypotension.
Nursing Measures:
Patients with hepatic impairment should receive lower dose.
Monitor blood pressure.Allow atleast 3 days between dosage adjustment to achieve steady
plasma levels.
Advise patient to report immediately if experiencing chest pain

23) NTG PATCH

Brand name: Deponit, Minitran, Nitrek, Nitro-Dur, Nitrodisc, Transderm-Nitro
Classification: Anti-Anginal Drugs
Dosage: Starting dose: 0.2-0.4 mg/hr. Dosing schedule: Daily patch-on period of 12-14 hr
& daily patch-off period of 10-12 hr.
Indication: Prevention of angina pectoris due to coronary artery disease
Action: a nitrate that reduces cardiac oxygen demand by decreasing left ventricular end
diastolic pressure and to a lesser extent, systemic vascular resistance, also increases blood
flow through collateral coronary vessels
Adverse Reactions: Headache. Transient episodes of lightheadedness. Infrequently,
hypotension. Syncope, crescendo angina, rebound HTN, allergic & anaphylactoid reactions.
Rarely severe, application site irritation.
Nursing Measures:
Administer transdermal systems to skin site free of hair and not subject to much
movement. Shave areas that have a lot of hair. Do not apply to distal extremities. Change
sites slightly to decrease the chance of local irritation and sensitization. Remove
transdermal system before attempting defibrillation or cardioversion.
To use transdermal systems, you may need to shave an area for application. Apply to a
slightly different area each day. Use care if changing brands; each system has a different
concentration.

24) PARACETAMOL

Brand name: Aeknil
Classification: Analgesics (Non-Opioid) & Antipyretics
Dosage: Adult & childn 10 yr 2-3 mL, 10 yr 1-2 mL. Depending on severity of case, dose
may be repeated 4 hrly. In severe cases, dose may be administered by IV very slowly
Indication: Pyrexia of unknown origin. Fever & pain associated w/ common childhood
disorders, tonsillitis, upper resp tract infections post-immunization reactions, after
tonsillectomy & other conditions. Prevention of febrile convulsion. Headache, cold, sinusitis,
muscle pain, arthritis & toothache
Action: produce analgesia by blocking pain impulses by inhibiting synthesis of prostaglandin
in CNS, relieves fever
Adverse Reactions: Hematological, skin & other allergic reactions
Nursing Measures:
Use liquid form for children and patients who have difficulty swallowing.
In children, dont exceed five doses in 24 hours.
Advise patient that drug is only for short term use and to consult the physician if giving to
children for longer than 5 days or adults for longer than 10 days.
Advise patient or caregiver that many over the counter products contain acetaminophen;
be aware of this when calculating total dailydose.
Warn patient that high doses or unsupervised long term use can cause liver damage.

25) PHENYTOIN

Brand name: Dilantin
Classification: Anticonvulsants
Dosage: Adult Initially 100 mg tid. Maintenance: 300-400 mg daily. Childn 6 yr Initially
100 mg tid, subsequent dosage should be adjusted according to therapeutic response, <6 yr
30 mg bid, may be increased to 30 mg tid or qid. Pedia 5 mg/kg/day Initially in 2-3 equally
divided doses. Max: 300 mg daily. Maintenance: 4-8 mg/kg/day
Indication: Tonic-clonic & complex partial (psychomotor, temporal lobe), prevention &
treatment of seizures occurring during or following neurosurgery
Action: may stabilize neuronal membranes and limit seizure activity by either by increasing
efflux or decreasing influx of Na ions across cell membrane in the motor cortex during
generation of nerve impulses
Adverse Reactions: GI disturbances; ataxia, slurred speech; diplopia, nystagmus & mental
confusion w/ headache, dizziness, gingival hyperplasia, hirsutism, hyperglycemia,
osteomalacia
Nursing Measures:
Assess location, duration, frequency, and characteristics of seizure activity. EEG may be
monitored periodically throughout therapy, Assess oral hygiene. Vigorous oral cleaning
beginning within 10 days of initiation of phenytoin therapy may help control gingival
hyperplasia.

26) TERBUTALINE

Brand name: Bricalin
Classification: Antiasthmatic & COPD Preparations
Dosage: Antiasthmatic & COPD Preparations
Indication: For reversible airways obstruction, in asthma, COPD. Decreases uterine
contractility & may be used to arrest premature labor
Action: relaxes bronchial smooth muscles by stimulating beta-2 receptors
Adverse Reaction: Fine tremor of skeletal muscle esp hands, palpitations, tachycardia,
nervous tension, headache, peripheral vasodilation.
Nursing Measures:
Use minimal periods of time; drug tolerance can occur with prolonged use.
Keep beta-adrenergic blocker readily available in case cardiac arrhythmias occur.
Do not recommended dosage.

27) VERAPAMIL HYDROCHLORIDE

Brand name: Calan, Calan SR, Covera-HS, Isoptin, Isoptin SR, Verelan, Verelan PM
Classification: Calcium Antagonists
Dosage: Isoptin tab Adult 40-80 mg tid-qid. Max: 480 mg daily. Childn >6 yr 40-120 mg
bid-tid, up to 360 mg daily, childn 6 yr 40 mg bid-tid. Isoptin SR 180 Coronary
insufficiency 1 tab bid. Usual daily dose: 240-480 mg. Hypertension 1 tab in the morning.
Isoptin SR 240 1 tab in the morning. If required after 2 wk, increase dose to 2 tab daily.
Isoptin amp 5 mg slow IV, if required, 5 mg after 5-10 min. Then, if required, continuous
drip infusion of 5-10 mg/hr up to 100 mg/day. Angina pectoris & rapid elimination of
tachyarrhythmias 1-2 amp IV, if required bid-tid
Indication: Isoptin/Isoptin SR 180 Essential hypertension, chronic coronary insufficiency,
angina pectoris, paroxysmal supraventricular tachycardia, tachyarrhythmias, long-term
treatment after MI. Isoptin SR 240 Essential hypertension
Action: decreases myocardial contractility and oxygen demand, it also dilates coronary
arteries and arterioles
Adverse Reactions: Constipation, dizziness, nausea. Rarely, vertigo, headache, hypotension,
ankle edema, flushing, fatigue, nervousness, erythromelalgia, paraesthesia, neuropathy;
bradycardiac arrhythmias, CHF. Dyspnea
Nursing Measures:
Monitor patient carefully (BP, cardiac rhythm, and output) while drug is being titrated to
therapeutic dose. Dosage may be increased more rapidly in hospitalized patients under
close supervision.
Ensure that patient swallows SR tablets whole: do not cut, crush, or chew them.
Monitor BP very carefully with concurrent doses of antihypertensives.
Monitor cardiac rhythm regularly during stabilization of dosage and periodically during
long-term therapy.
Administer sustained-release form in the morning with food to decrease GI upset.
Protect IV solution from light.
Monitor patients with renal or hepatic impairment carefully for possible drug accumulation
and adverse reactions.

28) IPRATROPIUM INHALATION

Brand name: Atrovent
Classification: Antiasthmatic & COPD Preparations, anticholinergics or antimuscarinics
Stock: 0.5 mg/2 mL
Dosage: Adult (including elderly) & adolescent >12 yr Acute attacks 1 vial, may repeat
doses until patient is stable. Maintenance: 1 vial tid-qid.
Indication: Bronchodilator for treatment of bronchospasm associated w/ COPD, including
chronic bronchitis, emphysema and asthma
Action: it works by binding to specific receptors (called muscarinic receptors) in the airway,
helping to relax the smooth muscle of the airway. When used to treat a runny nose, it works
by decreasing the production of fluid in the glands that line the nasal passages
Adverse Reaction: Headache, nausea, dry mouth, increased heart rate & palpitations, ocular
accommodation disturbances, GI motility disturbances, urinary retention, ocular side
effects, cough, local irritation, bronchoconstriction, skin rash, angioedema, urticaria,
laryngospasm, anaphylactic reactions.
Nursing Measures:
Protect solution for inhalation from light. Store unused vials in foil pouch.
Use nebulizer mouthpiece instead of face mask to avoid blurred vision or aggravation of
narrow-angle glaucoma.
Can mix albuterol in nebulizer for up to 1 hr.
Ensure adequate hydration, control environmental temperature to prevent hyperpyrexia.
Have patient void before taking medication to avoid urinary retention.
Teach patient proper use of inhalator.

29) FENOTEROL/IPRATROPIUM BROMIDE

Brand name: Berodual
Classification: Antiasthmatic & COPD Preparations
Dosage: Berodual inhalation soln Adult (including elderly) & adolescent >12 yr Treatment of
1 mL for immediate symptom relief. Intermittent & long-term treatment 1-2 mL for each
administration, up to qid. Moderate bronchospasm or w/ assisted ventilation 0.5 mL. Childn
6-12 yr Treatment of attacks 0.5-1 mL. Intermittent & long-term treatment 0.5-1 mL for
each administration, up to qid. Moderate bronchospasm or w/ assisted ventilation 0.5 mL.
Childn <6 yr (<22 kg body wt) Up to 0.5 mL up to tid. Berodual F UDV Adult & childn >12
yr Acute asthma episodes 1 vial, in very severe cases, 2 vials are needed. Intermittent &
long-term treatment 1 vial up to qid.
Indication: prevention and treatment of symptoms in chronic obstructive airway disorders
with reversible bronchospasm
Action: for the prevention and treatment of reversible bronchospasm associated with
bronchial asthma and especially chronic bronchitis with or without emphysema
Adverse Reactions: Fine tremor of skeletal muscles, nervousness, restlessness, palpitations;
less frequently tachycardia, dizziness or headache. Dry mouth, throat irritation or allergic
reactions, cough, paradoxical bronchoconstriction (rare). Urinary retention may occur in
particular, in patients w/ preexisting outflow tract obstruction.
Nursing Measures:
Protect solution for inhalation from light. Store unused vials in foil pouch.
Use nebulizer mouthpiece instead of face mask to avoid blurred vision or aggravation of
narrow-angle glaucoma.
Can mix albuterol in nebulizer for up to 1 hr.
Ensure adequate hydration, control environmental temperature to prevent hyperpyrexia.
Have patient void before taking medication to avoid urinary retention.
Teach patient proper use of inhalator.

30) BUDESONIDE

Brand name: Symbicort
Classification: Corticosteroids
Dosage: 80/4.5 mcg x 60 doses; 160/4.5 mcg x 60 doses; 320/9 mcg x 60 doses
Indication: regular treatment of asthma where use of a combination (inhaled corticosteroid
and long acting beta 2 agonist) is appropriate
Action: work by reducing inflammation, which helps with several conditions ranging from
asthma to allergies toCrohns disease
Adverse Reactions: Abdominal pain, conjunctivitis (pinkeye), cough, diarrhea, ear infection
or inflammation, fever, fungal infection in mouth, headache, nasal or sinus inflammation,
nosebleed, pain, rash, respiratory infection, stomach or intestinal inflammation, throat
inflammation, viral infection, vomiting, wheezing
Nursing Measures:
Taper systemic steroids carefully during transfer to inhalational steroids; deaths from
adrenal insufficiency have occurred.
Arrange for use of decongestant nose drops to facilitate penetration if edema, excessive
secretions are present.
Prime unit before use for Pulmicort Turbuhaler; have patient rinse mouth after each use.
Use aerosol within 6 mo of opening. Shake well before each use.
Store Respules upright and protected from light; gently shake before use; open envelopes
should be discarded after 2 wk.

31) ALBUTEROL AND IPRATROPIUM INHALATION

Brand name: Combivent
Classification: Bronchodilators
Stock: 2.5 mL
Dose: MDI Adult 2 puffs tid-qid. Max 12 puffs/day. Unit dose vial Adult & childn >12 yr 1
vial every 6-8 hr. Childn 2-12 yr 3 drops/kg/dose (max: 2500 mcg of salbutamol) every 6-8
hr.
Indication: management of reversible bronchospasm associated with obstructive airway
diseases in patients who require more than a single bronchodilator
Action: muscles in the airways and increase air flow to the lungs
Adverse Reactions: Fine tremor of skeletal muscle; palpitations; headache, dizziness,
nervousness; dryness of mouth, throat irritation; urinary retention
Nursing Measures:
Use nebulizer mouthpiece instead of face mask to avoid blurred vision or aggravation of
narrow-angle glaucoma.
Can mix albuterol in nebulizer for up to 1 hr.
Ensure adequate hydration, control environmental temperature to prevent hyperpyrexia.
Have patient void before taking medication to avoid urinary retention.
Teach patient proper use of inhalator.

32) SALBUTAMOL

Brand name: Aero-Vent
Classification: bronchodilator
Stock: 1 mg/1 mL
Dose: Adult & childn 2.5-5 mg. May repeat qid by hlebitis. Delivery of aerosol may be by
face mask of T piece. Use undiluted. For prolonged delivery time, dilute w/ sterile water or
normal saline for inj.
Indication: treatment of acute, severe asthma and in routine management of chronic
bronchospasm unresponsive to conventional therapy
Action: used with anti-inflammatory medication to prevent asthma attacks, Some of these
medicines are used to treat the symptoms of asthma, chronic bronchitis, emphysema, and
other lung diseases, while others are used to prevent the symptoms
Adverse Reactions: Dizziness, severe; feeling of choking, irritation, or swelling in throat;
flushing or redness of skin; hives; increased shortness of breath; skin rash; swelling of face,
lips, or eyelids; tightness in chest or wheezing, troubled breathing
Nursing Measures:
Assess lung sounds, pulse, and blood pressure before administration and during peak of
medication. Note amount, color, and character of sputum produced.
Monitor pulmonary function tests before initiating therapy and periodically throughout
course to determine effectiveness of medication.
Observe for paradoxical bronchospasm (wheezing). If condition occurs, withhold
medication and notify physician or other health care professional immediately.
Instruct mother to take missed dose as soon as remembered, spacing remaining doses at
regular intervals. Do not double doses or increase the dose or frequency of doses.
Inform the mother not to smoke near the child and to avoid respiratory irritants.
Advise the mother to rinse the childs mouth with water after each inhalation dose to
minimize dry mouth.

33) TERBUTALINE SULFATE

Brand name: Pulmonyl
Classification: Antiasthmatic/ Brochodilator
Stock: 2.5 mg/ml
Dose: Adult 5-10 mg, Children 2-5mg
Indication: relief of bronchospasm in obstructive airway diseases
Action: It works by dilating (opening) the bronchioles of the lungs by relaxing the muscles
around them. This allows for easier airflow into and out of the lungs
Adverse Reactions: Headache, nausea, vomiting, palpitations, tachycardia, sweating &
drowsiness
Nursing Measures:
Use minimal periods of time; drug tolerance can occur with prolonged use.
Keep beta-adrenergic blocker readily available in case cardiac arrhythmias occur.
Do not recommended dosage.

34) HEPARIN SODIUM

Brand name: Britton Heparin Na
Classification: Anticoagulants, Antiplatelets & Fibrinolytics (Thrombolytics)
Dosage: 5000 iu/1 mL; 25000 iu/1 mL
Indication: treatment and prophylaxis of thromboembolic disorders
Action: Accelerates formation of antithrombin III-thrombin complex and deactivates
thrombin, preventing conversion of fibrinogen to fibrin
Adverse Reactions: Slight fever, headache, chills, nausea, vomiting, constipation, epistaxis,
bruising, slight haematuria, skin necrosis (SC inj), osteoporosis, alopecia. Hypersensitivity
reactions include urticaria, conjunctivitis, rhinitis, asthma, angioedema and anaphylactic
shock. Priapism. Potentially Fatal: Heparin-induced thrombocytopenia with or without
thrombosis; bleeding
Nursing Measures:
Baseline blood coagulation tests, Hct, Hgb, RBC and platelet counts prior to initiation or
therapy and at regular intervals throughout therapy
Monitor APTT levels closely
Draw blood for coagulation tests 30 min before each scheduled SC or intermittent IV dose
and approximately q4h for pts receiving continuous IV heparin during dosage adjustments
period. After dosage is established, tests may be done once daily
Pts vary widely in their reaction to heparin; risk of hemorrhage appears greatest in
women, all patients > 60 y, and patients with liver disease or renal insufficiency.
Monitor vitals, report fever, drop in BP, rapid pulse and other S&S of hemorrhage
Observe all needle sites daily for hematoma and signs of inflammation
Have on hand protamine sulfate, specific heparin antagonist

35) ESMOLOL HYDROCHLORIDE

Brand name: Brevibloc
Classification: Beta blockers
Dosage: 100mg/10ml
Indication: supraventricular tachycardia; post-operative tachycardia or hypertension; non-
compensatory sinus tachycardias; intra-operative tachycardia or hypertension; unstable
angina, non ST segment elevation MI
Action: A Class II antiarrythmic and ultra-short-acting selective beta blocker that decreases
heart rate, contractility and blood pressure
Adverse Reactions: Hypotension, bradycardia, heart failure, local irritation, diaphoresis,
peripheral ischaemia, dizziness, somnolence, confusion, fatigue, paraesthesia, peripheral
neuropathy, headache, weakness, irritability, dyspnoea, nausea, vomiting, blurred vision,
urinary retention, fever, rigor, muscular pain. Potentially Fatal: Profound bradycardia, AV
block, cardiogenic shock, asystole, bronchospasm.
Nursing Measures:
Monitor patient carefully (BP, cardiac rhythm, and output) while drug is being titrated to
therapeutic dose. Dosage may be increased more rapidly in hospitalized patients under
close supervision.
Monitor cardiac rhythm regularly during stabilization of dosage and periodically during
long-term therapy.

36) D 50-50

Brand name: Phil Pharmawealth/Atlantic 50% Dextrose
Classification: Intravenous & Other Sterile Solutions
Dosage: 50ml/vial
Indication: for hypoglycemia
Action: A simple water soluble sugar that minimizes glyconeogenesis and promotes
anabolism in patients whose oral caloric intake is limited
Adverse Reactions: Local pain, vein irritation, thrombophlebitis & tissue necrosis in the
event of extravasation. Fluid & electrolyte imbalance eg hypokalemia, hypomagnesemia &
hypophosphatemia; edema or water intoxication
Nursing Measures:
Monitor infusion rate frequently; if signs of fluid overload, turn off IV drip. Infusion may
result in fluid overload.
Check IV site frequently and if infiltration is noted, turn off IV drip.
Watch out for signs of fluid overload (distended neck veins (JVD), rapid respirations,
shallow tidal volume, fine auscultatory crackles, dyspnea, and peripheral edema)
Watch out for signs of infiltration (swelling and pain around IV site).

37) POTASSIUM CHLORIDE

Brand name: Phil Pharmawealth/Atlantic Potassium Chloride
Classification: Electrolytes
Dosage: 40 meqs/20 ml
Indication: for hypokalemia, acute MI
Action: Replaces potassium and maintains potassium level
Adverse Reactions: GI ulceration (sometimes with haemorrhage and perforation or with late
formation of strictures) following the use of enteric-coated K chloride preparation;
hyperkalaemia. Oral: Nausea, vomiting, phlebiti and abdominal cramps. IV: Pain or
phlebitis; cardiac toxicity.
Nursing Measures:
Monitor serum potassium levels, renal function, and serum bicarbonate.
Explain to patient purpose of the medication and the need to take as directed,especially
when concurrent digoxin or diuretics are taken. A missed dose should be taken as soon as
remembered within 2 hr; if not, return to regular doseschedule. Do not double dose.
Emphasize correct method of administration. GI irritation or ulceration may result from
chewing enteric-coated tablets or insufficient dilution of liquid or powder forms. Some
extended-release tablets are contained in a wax matrix that may be expelled in the stool.
This occurrence is not significant.
Instruct patient to avoid salt substitutes or low-salt milk or food unless approved by health
care professional.
Patient should be advised to read all labels to prevent excess potassium intake.
Advise patient regarding sources of dietary potassium.
Encourage compliance with recommended diet.
Instruct patient to report dark, tarry, or bloody stools; weakness; unusual fatigue; or
tingling of extremities.
Notify health care professional if nausea, vomiting, diarrhea, or stomach discomfort
persists.
Dosage may require adjustment. Emphasize the importance of regular follow-up exams to
monitor serum levels and progress.

38) LIDOCAINE HYDROCHLORIDE

Brand name: Abbott Lidocaine
Classification: Anaesthetics - Local & General
Dosage: 50 ml/vial
Indication: local or regional anesthesia
Action: A class IB antiarrythmic that decreases the depolarization, automaticity, and
excitability in the ventricles during the diastolic phase by direct action on the tissues
especially the Purkinje network
Adverse Reactions: Restlessness, nervousness, dizziness, tinnitus, blurred vision; GI upsets;
muscle twitching, convulsions; numbness of the tongue; hypotension, bradycardia;
methemoglobinaemia; fetal intoxication.
Nursing Measures:
Check drug concentration carefully; many concentrations are available.
Reduce dosage with hepatic or renal failure.
Continuously monitor response when used as antiarrhythmic or injected as local
anesthetic.
Keep life-support equipment and vasopressors readily available in case severe adverse
reaction (CNS, CV, or respiratory) occurs when lidocaine is injected.
Establish safety precautions if CNS changes occur; have IV diazepam or short-acting
barbiturate (thiopental, thiamylal) readily available in case of seizures.
Monitor for malignant hyperthermia (jaw muscle spasm, rigidity); have life-support
equipment and IV dantrolene on standby.
Titrate dose to minimum needed for cardiac stability, when using lidocaine as
antiarrhythmic.
Reduce dosage when treating arrhythmias in CHF, digitalis toxicity with AV block, and
geriatric patients.
Monitor fluid load carefully; more concentrated solutions can be used to treat arrhythmias
in patients on fluid restrictions.
Have patients who have received lidocaine as a spinal anesthetic remain lying flat for 612
hr afterward, and ensure that they are adequately hydrated to minimize risk of headache.
Check lidocaine preparation carefully; epinephrine is added to solutions of lidocaine to
retard the absorption of the local anesthetic from the injection site. Be sure that such
solutions are used
only to produce local anesthesia. These solutions should be injected cautiously in body
areas supplied by end arteries and used cautiously in patients with peripheral vascular
disease, hypertension, thyrotoxicosis, or diabetes.
Use caution to prevent choking. Patient may have difficulty swallowing following use of
oral topical anesthetic. Do not give food or drink for 1 hr after use of oral anesthetic.
Treat methemoglobinemia with 1% methylene blue, 0.1 mg/kg, IV over 10 min.
Apply lidocaine ointments or creams to a gauze or bandage before applying to the skin.
Monitor for safe and effective serum drug concentrations (antiarrhythmic use: 15
mcg/mL). Doses > 610 mcg/mL are usually toxic

39) SODIUM BICARBONATE

Brand name: Hospira Sodium Bicarbonate
Classification: Alkalinizers
Dosage: 10mEq/10ml; 50mEq/50ml
Indication: metabolic acidosis, systemic or urinary alkalinization, antacid, cardiac arrest
Action: Restores buffering capacity of the body and neutralizes excess acid
Adverse Reaction: Tetany, edema, gastric distention, belching, flatulence, hypokalemia,
metabolic alkalosis, hypernatremia, chemical cellulitis because of alkalinity, pain, irritation,
tissue necrosis, ulceration or sloughing at the site of infiltration
Nursing Measures:
do not take drug with milk to avoid hypercalcemia, abnormally high alkalinity in tissues
and fluids, or kidney stones.
do not give to patients with metabolic or respiratory alkalosis, and in those with
hypocalcemia in which alkalosis may produce tetany, hypertension, seizures, or heart
failure.
monitor for alkalosis by obtaining blood pH, PaO2, PCO2, and electrolyte levels

40) DOPAMINE

Brand name: Intropin
Classification: Adrenergics (Sympathomimetics)
Dosage: 40 mg/Ml; 80mg/mL; 160 mg/mL
Indication : shock and hemodynamic imbalances, hypotension
Action: Stimulates dopaminergic and alpha beta receptors for the sympathetic nervous
system resulting in a positive inotropic effect and increased cardiac output. Action is dose-
related; large doses cause mainly alpha stimulation
Adverse Reaction: ectopic beats, tachycardia, anginal pain, palpitation, hypotension,
vasoconstriction, ventricular arrhythmias, hypertension, headache, anxiety, dilated pupils,
nausea, vomiting, decreased urine output, dyspnea
Nursing Measures:
Monitor vital signs and ECG closely throughout therapy.
Monitor I&O regularly; note decreases in urine output.
Monitor central venous pressure or pulmonary wedge pressure if possible during infusion.
Note significant changes in vital signs, ECG changes, deterioration of peripheral pulses,
and/or cold, mottled extremities

41) DOBUTAMINE

Brand name: Dobatrey
Classification: Adrenergics
Dosage: 12.5 mg/mL
Indication: increased cardiac output in short term treatment of cardiac decompensation
caused by depressed contractility
Action: Stimulates hearts beta1 receptors to increase myocardial contractility and stroke
volume. Increases cardiac output by decreasing peripheral vascular resistance, reducing
ventricular filling pressure, and facilitating AV node conduction
Adverse Reaction: increased systolic BP, increased heart rate, chest pain, increased number
of premature ventricular beats, headache, tingling sensations, paresthesia. nausea,
vomiting, dyspnea, phlebitis, local inflammation after infiltration, leg cramps
Nursing Measures:
Monitor vital signs, ECG, cardiac output, pulmonary capillary wedge pressure, central
venous pressure and urinary output carefully throughout infusion.
Monitor patency and placement of IV catheter to reduce risk of extravasation and
phlebitis.
Watch out for symptoms of overdosage such as excessive hypertension, tachycardia,
nausea, vomiting, tremor, headache, chest pain

42) LIDOCAINE PREMIXED

Brand name: Xylocaine
Classification: Antiarrhythmic agent, Local anesthetic
Dosage: 0.2% (2mg/ml); 0.4% (4g/ml); 0.8% (8g/ml)
Indication: ventricular arrhythmias caused by MI, cardiac manipulation or cardiac glycosides
Action: Acts as an anesthetic by stabilizing the neuronal membrane by inhibiting the ionic
fluxes required for the initiation and conduction of impulses, thereby effecting local
anesthetic action. Also acts as an antiarrhythmic by decreasing the depolarization,
automaticity, and excitability in the ventricles during the diastolic phase by a direct action
on the tissues, especially the Purkinje network, without involvement of the autonomic
system. Neither contractility, systolic arterial blood pressure, atrioventricular (AV)
conduction velocity, nor absolute refractory period is altered by usual therapeutic doses
Adverse Reaction: bradycardia, cardiac arrest, CV collapse, hypotension, apprehension,
confusion, dizziness, drowsiness, hallucinations, headache, light-headedness, mood
changes, nervousness, tremors, conjunctival hyperemia, corneal epithelial changes,
diplopia, tinnitus, visual disturbances, nausea, vomiting, erythema, petechiae, edema,
injection-site reactions, including bruising, burning, contusion, hemorrhage, local reactions,
including soreness at IM injection site, venous thrombosis or phlebitis, extravasation,
burning, stinging, sloughing, respiratory depression or arrest, hypersensitivity reactions
Nursing Measures:
Explain that adverse reactions related to the CNS (eg, drowsiness, confusion,
paresthesias, convulsions, respiratory arrest) can occur and are a result of CNS toxicity.
Advise patient that drug may cause dizziness or drowsiness and to avoid getting out of
bed or walking without assistance.
Advise patients that skin reactions, including erythema, petechiae, and edema, may occur
with intradermal injection.
Systemic effects can occur following topical use; use lowest possible dose to avoid serious
toxicity, shock, or heart block.
Do not use in patients with congenital or idiopathic methemoglobinemia or in infants
younger than 12mo of age who are receiving methemoglobin-inducing drugs.
Use with caution and in lower doses in patients with CHF, reduced cardiac output, digitalis
toxicity, and in elderly patients

43) MANNITOL

Brand name: Osmitrol
Classification: osmotic diuretic
Dosage: 5% , 10%, 15%, 20%, 25% in 500cc/1,000cc
Indication: test dose for marked oliguria or suspected inadequate renal function, oliguria, to
reduce intraocular or intracranial pressure, diuresis in drug intoxication
Action: Increases osmotic pressure of glomerular filtrate; drug elevates plasma osmolality
Adverse Reaction: Increased urination, nausea, runny nose, vomiting, severe allergic
reactions (rash, hives, itching, difficulty breathing, tightness in the chest, swelling of the
mouth, face, lips, or tongue), blurred vision, chest pain, chills or fever, confusion, decreased
alertness, difficulty urinating, extreme dizziness, extreme thirst or dry mouth, fast or
irregular heartbeat, headache, muscle cramps, pain, redness, or swelling at the injection
site, weakness
Nursing Measures:
Monitor vital signs, including CVP, and fluid intake and output.
Monitor weight, renal function, and serum sodium and potassium levels daily
Watch out for symptoms of overdosage such as excessive hypertension, tachycardia,
nausea, vomiting, tremor, headache, chest pain
To relieve thirst, give frequent mouth care and fluids

44) DEXTROSE 5% IN WATER (D5W) SOLUTION

Brand name: None
Classification: Isotonic/Hypotonic Solution
Dosage: 250ml bottles (5g dextrose/100ml water)
Indication: fluid replacement and caloric supplementation in patients who cant maintain
adequate oral intake or are restricted from doing so
Action: Provides some sugar for cellular metabolism and supplies body water
Adverse Reaction: Increases free water and may cause intracellular edema, fluid overload,
infiltration (swelling and pain at infusion site)
Nursing Measures:
Monitor infusion rate frequently; if signs of fluid overload, turn off IV drip. Infusion may
result in fluid overload.
Check IV site frequently and if infiltration is noted, turn off IV drip.
Watch out for signs of fluid overload (distended neck veins (JVD), rapid respirations,
shallow tidal volume, fine auscultatory crackles, dyspnea, and peripheral edema)
Watch out for signs of infiltration (swelling and pain around IV site).