NREMT ALS Meds Flashcards

1
Q

Enalapril, Captopril, Lisinopril, Ramipril, et al

A

Trade Name(s): Vasotec®, Lotensin®, Accupril®, Altace®, Zestril®, et al

Class: Angiotensin-converting enzyme (ACE) inhibitor, antihypertensive

Description: ACE inhibitors interfere with the development of angiotensin II, reducing peripheral vascular resistance, blood pressure and cardiac afterload.

Indication(s): Hypertension, AMI or heart failure without hypotension.

Contraindication(s): Pregnancy, elevated serum potassium, hypotension (SBP<100), hypovolemia, Hx of angioedema, or hypersensitivity to the drug.

Precautions: Renal failure.

Dosage/Administration: Enalapril-2.5mg PO, 1.25 mg IV over 5 minutes (IV form can be contraindicated in STEMI); Captoril-6.25 to 25 mg PO; Lisinopril-2.5 to 10 mg PO; Ramipril-2.5 mg PO.

Special Considerations: Watch for ACE inhibitor induced angioedema and chronic cough (from increased bradykinin levels).

Captopril is on NJ Formulary.

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2
Q

Adenosine

A

Trade Name(s): Adenocard®

Class: Antiarrhythmic

Description: Adenosine is a naturally occurring agent (endogenous nucleoside) that can “chemically cardiovert” SVT to a normal sinus rhythm

Indication(s): Narrow complex, supraventricular tachycardia refractory to vagal maneuvers or to facilitate diagnosing tachycardia of unknown origin.

Contraindication(s): Hypersensitivity, 2° and 3° AV block and sick sinus syndrome (without a pacemaker), severe hypotension. Relative in asthma.
Precautions: May cause transient dysrhythmias

Dosage/Administration: 6 mg rapid IV push, immediately followed by a rapid flush of saline. If ineffective after 1-2 minutes, give 12 mg. If still ineffective, 12 mg may be repeated once. Ped: 0.1mg/kg to a maximum dose of 6 mg rapid IV push, immediately followed by a rapid saline flush. If ineffective after 1-2 minutes give 0.2mg/kg to a maximum dose of 12 mg rapid IV push. If still ineffective 0.2mg/kg dose may repeated once.

Special Considerations: Adenosine has a half life of less then 10 seconds. It, therefore, must be pushed rapidly. An IV site which is most proximal to the heart should be utilized. Also, use the largest gauge angio that the vein can accommodate. Brief asystole is common after injection and does not persist to cardiac arrest.. Less effective in patients taking theophylline or caffeine. Reduce initial dose in patients receiving dipyridamole, carbamazepine, heart transplants, or via central line.

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3
Q

Albuterol

A

Trade Name(s): Proventil®, Ventolin®, Proair®

Class: Sympathomimetic, Bronchodilator, Beta-2 Agonist

Description: Albuterol is a synthetic sympathomimetic that causes bronchodilation with less cardiac effect than epinephrine. It also reduces mucus secretion, pulmonary capillary leakage and edema in the lungs during allergic reactions.

Indication(s): Prevention and treatment of reversible bronchospasm associated with asthma and other obstructive pulmonary diseases. Commonly used to treat Hyperkalemia. Shifts potassium intracellularly due to Beta-2 specific adrenergic stimulation, therefore reducing overall serum potassium levels.

Contraindication(s): Hypersensitivity to the drug or any of its components.

Precautions: The patient may experience tachycardia, anxiety, nausea, cough, wheezing, and/or dizziness. Vital signs and breath sounds must be monitored. Use
caution with elderly, cardiac or hypertensive patients.

Dosage/Administration: Two inhalations (90 mcg) via metered dose inhaler or
2.5 mg in 2.5-3 ml NS via nebulizer, repeat as needed. The duration of the effect is
3-6 hours. Ped: 0.15 mg/kg in 2.5 to 3 ml NS via nebulizer, repeat as necessary.

Special Considerations: Beta-blockers are Antagonistic; May potentiate hypokalemia.

Onset: approximately 15 mins.

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4
Q

Aminophylline

A

Trade Name(s): Truphylline®, Somohyllin®

Class: Methylxanthine bronchodilator

Description: Aminophylline is a methylxanthine that prolongs bronchodilation and decreases mucus production and has mild cardiac and CNS stimulating effects.

Indication(s): Bronchospasm in asthma and COPD refractory to sympathomimetics and other bronchodilators.

Contraindication(s): Hypersensitivity to methylxanthines or uncontrolled cardiac
dysrhythmias

Precautions: Cardiovascular disease, hypertension, hepatic impairment, diabetes, hyperthyroidism, glaucoma, peptic ulcers, acute influenza, recent influenza immunization, young children, the elderly, and those taking theophylline.

Dosage/Administration: 250-500 mg IV over 20-30 mins. Ped: 6mg/kg over 20-
30 mins to a maximum of 12/kg/day

Special Considerations: Seldom used due to narrow therapeutic index before
toxicity

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5
Q

Amiodarone

A

Trade Name(s): Cordarone®, Nexterone®, Pacerone®

Class: Antiarrhytmic

Description: Amiodarone is an antiarrhythmic that prolongs the duration of the
action potential and refractory period through sodium, potassium, and calcium
channels; blocks alpha and beta adrenergic receotors; relaxes smooth muscles,
reducing peripheral vascular resistance and increasing coronary flow.

Indication(s): Life-threatening and refractory VF, VT, and supraventricular
tachydysrhythmias.

Contraindication(s): Hypersensity to the drug, cardiogenic shock, severe sinus
bradycardia and advanced heart block.

Precautions: Hepatic impariment, pregnancy, breastfeeding

Dosage/Administration: Refractory VF/pVT: 300 mg IV push, second dose of
150 mg IV push. Perfusing VT/ rapid infusion: 150mg IV over 10 minutes.
Maintenance/slow infusion 360mg over next 6 hours (1mg/min) then infusion
540mg over 18 hours (0.5mg/min). Max dose 2.2g/24 hours. Ped: Refractory
Pulseless Ventricular Tachycardia and Ventricular Fibrillation 5 mg/kg, then repeat
to a total dose of 15 mg/kg. Ped: 5 mg/kg IV/IO over 20-60 minutes, can be
repeated up to a total dose of 15 mg/kg.

Special Considerations: May drop blood pressure when administered; give
slowly (IV drip) when patient has a pulse, push only when pulseless/cardiac arrest.
Amiodarone itself can be thyrotoxic and delivers a large iodine load which can
effect patients with hypo- or hyperthyroid. In pregnancy, exposure may cause fetal
harm

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6
Q

Amyl Nitrite

A

Trade Name(s): Amyl nitrite

Class: Cyanide poisoning adjunct, antidote, vasodilator

Description: Amyl nitrite is a short-acting vasodilator similar to nitroglycerin. It
binds with hemoglobin to form methemoglobin which preferentially binds cyanide,
releasing it from the cytochrome.

Indication(s): Acute cyanide poisoning

Contraindication(s): None in the case of acute cyanide poisoning.

Precautions: None

Dosage/Administration: 0.3 mL ampule crushed and contents poured onto a
gauze and placed in front of patient’s mouth or endotracheal tube, if patient
intubated, to be inhaled over 15-30 sec; repeat q 1 min. until IV sodium nitrite
available. Each ampule lasts approximately 3 min; separate administration by at
least 30 sec to allow patient to adequate oxygenate.

Special Considerations: Part of cyanide antidote kit which also includes sodium
nitrate and sodium thiosulfate.

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7
Q

Aspirin, Acetylsalicylic Acid (ASA)

A

Trade Name(s): Empirin®, Ecotrin®, Halfprin®, Zorprin®

Class: Antipyretic, analgesic, platelet inhibitor, anti-inflammatory

Description: Aspirin inhibits agents that cause the production of inflammation,
pain and fever. It also powerfully inhibits platelet aggregation.

Indication(s): Cardiogenic chest discomfort

Contraindication(s): Hypersensitivity to salicylates, active ulcer disease

Precautions: Allergies to other NSAIDs, bleeding disorders, children or teenagers
with varicella or influenza-like symptoms, asthma

Dosage/Administration: 160-325 mg PO (chewable, non-enteric coated).
Special Considerations: Platelet aggregation effects take place in 15 minutes and
last approximately 4 days

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8
Q

Atropine sulfate

A

Trade Name(s): Sal-Tropine®

Class: Parasympatholytic, anticholinergic

Description: Atropine blocks the parasympathetic nervous system, specifically
the vagal effects on the heart rate. It does not increase contractility but may
increase myocardial oxygen demand. It also decreases airway secretions.

Indication(s): Hemodynamically significant bradycardia and organophosphate
poisoning.

Contraindication(s): None in the emergency setting.

Precautions: AMI, Glaucoma, hypothermic bradycardia.

Dosage/Administration: Symptomatic Bradycardia: 0.5-1 mg rapid IV push,
repeat q 3-5 min to a max of 3 mg. Pediatric dose: 0.02mg/kg rapid IV push, may
be repeated once up to 1 mg for a child or 3 mg for an adolescent. Can be given
via ETT 0.04-0.06 mg/kg. Organophosphate Poisoning: 2-4 mg IV/IO repeated
until symptomatic improvement. Pediatric dose: <12 years old 0.02-0.05 mg/kg
IV/IO q 20-30 min, as needed.

Special Considerations: If pushed too slowly or if less than the recommended
dosage is given the result will be paradoxical bradycardia

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9
Q

Bumetanide

A

Trade Name(s): Bumex®
Class: Loop Diuretic

Description: Bumetanide is related to furosemide, however it has a faster rate of
onset, greater diuretic potency (40 times), shorter duration and produces only mild
hypotension.

Indication(s): Diuresis in CHF and pulmonary edema.

Contraindication(s): Hypersensitivity to bumetanide or other sulfonamides.

Precautions: Pregnancy-it should only be used in life-threatening conditions.
Dosage/Administration: 0.5-1 mg IM/IV over 1-2 minutes, repeat in 2-3 hours as
needed

Special Considerations: Usually used if furosemide shortage.

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10
Q

Calcium Chloride

A

Trade Name(s): Calcium Chloride

Class: Electrolyte

Description: Calcium chloride increases myocardial contractile force and
increases ventricular automaticity.

Indication(s): Hyperkalemia, hypocalemia, hypermagnesemia, calcium channel
blocker toxicity

Contraindication(s): Ventricular fibrillation, hypercalcemia, possible digitalis
toxicity.

Precautions: May precipitate toxicity in patients taking digoxin. .

Dosage/Administration: 500-1000 mg IV (5-10 ml of 10% solution) as needed.
Ped: 20mg/kg IV/IO, as needed.

Special Considerations: Ensure the IV line is in a large vein and flushed before
and after using calcium. Painful, burning sensation when administered rapidly or
in a small vein. Can cause vein sclerosis. Precipitates when mixed with Sodium
Bicarbonate.

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11
Q

Calcium Gluconate

A

Trade Name(s): Kalcinate®

Class: Electrolyte

Description: Counteracts the toxicity of hyperkalemia by stabilizing the
membranes of the cardiac cells, reducing the likelihood of fibrillation; increases
myocardial contractile force & ventricular automaticity.

Indication(s): Hyperkalemia, hypocalemia, hypermagnesemia, calcium channel
blocker toxicity

Contraindication(s): Ventricular fibrillation, hypercalcemia, possible digitalis
toxicity.

Precautions: May precipitate toxicity in patients taking digitalis, with renal and
cardiac insufficiency, and immobilized patients.

Dosage/Administration: Hyperkalemia 500-1,000mg slow IV/IO push,
maximum of 3 grams. Beta blocker and calcium channel blocker overdose 3-6
grams IV/IO; followed by a continuous hourly infusion of the same dose.
Pediatric: Hyperkalemia 60-100mg/hour IV/IO slowly over a 5-10 minutes to a
maximum of 3 grams. Beta blocker and calcium channel blocker overdose:
60mg/kg IV/IO followed by a continuous hourly infusion of the same dose.

Special Considerations: Do not administer by IM or Sq; causes significant tissue
necrosis. Less potent than calcium chloride (calcium chloride has 3 times as much
calcium)

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12
Q

Dexamethasone Sodium Phosphate

A

Trade Name(s): Decadron®

Class: Corticosteroid, Adrenal Glucocorticoid

Description: Long-acting adrenocorticoid with intense anti-inflammatory activity.
It prevents the accumulation of inflammation generating cells at the sites of
infection or injury.

Indication(s): Anapylaxis, asthma and COPD, Moderate to severe Croup

Contraindication(s): There are no absolute contraindications in the emergency
setting. Relative contraindications include, systemic fungal infections, actue
infections, tuberculosis, vaccine or live virus vaccinations.

Precautions: Herpes simplex, keratitis, myasthenia gravis, hepatic or renal
impairment, diabetes, CHF, seizures, psychiatric disorders, hypothyroidism and GI
ulceration.

Dosage/Administration: 2-100mg IV/IM Peds: 0.5-1 mg/kg

Special Considerations: Immunosuppressive effects.

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13
Q

Dextrose, (D50W, D25W, D10W, D5W)

A

Trade Name(s): Dextrose

Class: Carbohydrate

Description: Dextrose is a simple sugar that the body can rapidly metablozie to
create energy.Short term osmotic diuresis.

Indication(s): Hypoglycemia, Hyperkalemia

Contraindication(s): None in the presence of hypoglycemia.

Precautions: Increased ICP or intracranial hemmorhage. Determine blood
glucose level prior to administration.

Dosage/Administration:
Adult:25g D50W (50ml) IV push. Peds: >1 month 0.5-
1.0 g/kg of a 25% solution IV/IO, 0.5 g/kg of a 10% dextrose solution IV/IO for <1
month old.
Special Considerations: When establishing an IV to administer D50W, utilize the
largest vein available and use the largest catheter the vein can
accomadate.Extravasation leads to tissue necrosis.

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14
Q

Diazepam

A

Trade Name(s): Valium®

Class: Antianxiety/Hypnotic/Anticonvulsant/Sedative.

Description: Diazepam is a benzodiazepine sedative and skeletal muscle relaxant
that reduces tremors, induces amnesia and reduces the incidence and recurrence of
seizures. It relaxes muscle spasms in orthopedic injuries and produces amnesia in
painful procedures (e.g., synchronized cardioversion)

Indication(s): Seizures, status epilepticus, premedication before cardioversion,
muscle tremors due to injury, muscle spasm and acute anxiety.

Contraindication(s): Hypersensity to drug, shock, coma, acute alchoholism,
depressed vital signs, obstetric patients and neonates.

Precautions: Psychosis, hypotension, mental status depression, respiratory
depression.

Dosage/Administration: Seizures: 5-10 mg IV/IM, Peds: 0.5-2mg IV/IM.
Acute Anxiety: 2-5 mg IV/IM, Peds: 0.5-2mg IM Premedication:5-15 mg IV
Peds: 0.2-0.5mg/kg IV. Available as rectal gel for pediatrics.

Special Considerations: Has a longer half life than other benzodiazepines but is redistributed to fat so serum concentrations decrease faster. Parents may
administer to children with epilepsy who are seizing prior to EMS arrival. As with
all opiates, push slowly

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15
Q

Diltiazem

A

Trade Name(s): Cardizem®

Class: Calcium Channel Blocker

Description: Diltiazem is a slow calcium channel blocker similar to verapamil. It
dilates coronary and periphreal arteries and arterioles, thus increasing circulation to
the heart and reducing peripheral vascular resistance.

Indication(s): Supraventricular tachydysrhythmias (ie atrial fibrillation, atrial
flutter and PSVT refractory to adenosine) and to increase coronary artery perfusion
in angina.

Contraindication(s): Hypersensitivity, sick sinus syndrome, 2nd or 3rd-degree
heart block, systolic BP <90, diastolic BP <60, wide-complex tachycardia and
WPW.

Precautions: CHF (especially with beta blockers), conduction abnormalities,
renal or hepatic impairment, the elderly and nursing mother.
Dosage/Administration: 0.25 mg/kg (15-20 mg) slow IV push over 2 minutes,
may repeat in 15 minutes with 0.35 mg/kg (20-25 mg) slow IV push over 2
minutes.

Special Considerations: Continuous EKG monitoring and frequent measurement
of blood pressure.

Comparing Calcium Channel Blockers: Verapamil is mostly
cardiac effects, nicardipine/nifedipine/amlodipine are mostly peripheral effects
and diltiazem is somewhere in the middle.

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16
Q

Diphenhydramine

A

Trade Name(s):Benadryl®

Class: Antihistamine, Anticholinergic

Description: Diphenhydramine blocks histamine release, thereby reducing
histamine-induced bronchoconstriction, vasodilation and edema.

Indication(s): Anaphylaxis, allergic reactions, motion sickness and acute dystonic
extrapyramidal reactions to antipsychotic drugs.

Contraindication(s): Hypersensitivity; narrow-angle glaucoma

Precautions: May induce hypotention, headache, palpitations, tachycardia,
sedation, drowsiness and/or disturbed coordination; Asthma and other lower
respiratory disease.

Dosage/Administration: 25-50 mg IV/IM Peds:2-5 mg/kg

Special Considerations: Will potentiate actions and side effects of narcotics and
other CNS depressants; cannot be given SQ; give either IV or deep IM injection

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17
Q

Dobutamine Hydrochloride

A

Trade Name(s): Dobutrex®

Class: Sympathomimetic

Description: Dobutamine is a synthetic catecholamine and beta agent that
increases the strength of cardiac contraction without appreciably increasing rate.

Indication(s): To Increase cardiac output in congestive heart failure and
cardiogenic shock.

Contraindication(s): Hypersensitivity to sympathomimetic amines, ventricular
tachycardia and hypovolemia without fluid rescucitation.

Precautions: Atrial fibrillation or preexisting hypertention.

Dosage/Administration: 2-20 mcg/kg/min IV titrated to effect. Peds: same as
adult.

Special Considerations:
During the administration of dobutamine EKG and
blood pressure should be continuously monitored. Hypovolemia should be
corrected with suit-able volume expanders before treatment with dobutamine is
instituted. Dobutamine can worsen hypotension

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18
Q

Dopamine Hydrochloride

A

Trade Name(s): Intropin®

Class: Sympathomimetic, Vasopressor, Inotropic Agent

Description: Dopamine is a naturally occuring catecholamine that increases
cardiac output without appreciably increasing mycardial oxygen consumption. It
maintains renal and mesenteric blood flow while inducing vasoconstriction and
increasing systolic blood pressure.

Indication(s): Used in the treatment of hypotension, low cardiac output, poor
perfusion of vital organs; used to increase mean arterial pressure in septic shock
patients who remain hypotensive after adequate volume expansion.

Contraindication(s): Hypovolemic hypotension without aggressive fluid
resuscitation, tachydysrhythmias, ventricular fibrillation and pheochromocytoma
(a rare adrenal gland cancer).

Precautions: Occlusive vascular disease, cold injury, arterial embolism.
Dosage/Administration: 5-20 mcg/kg/min titrate to desired SBP/MAP.
Theoretically doses less that 5 mcg/kg/min have predominately renal effects

Special Considerations: Use caution in patients taking MAO inhibitors. Ensure
adequate fluid resuscitation of the hypovolemic patient prior to use.

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19
Q

Epinephrine

A

Generic Name: Epinephrine

Trade Name(s): Adrenalin®, EpiPen®, Adrenaclick®

Class: Sympathomimetic

Description: Epinephrine is a naturally occurring catecholamine that increases
heart rate, cardiac contractile force, myocardial electrical activity and automaticity.
It also, through bronchial artery constriction, may reduce pulmonary congestion
and increase tidal volume.

Indication(s): Cardiac arrest, anaphylaxis, hypotension, symptomatic bradycardia,
bronchospasm, upper airway edema

Contraindication(s): Hypersensitivity to sympathomimetic amines, narrow-angle
glaucoma; hemorrhagic, tramatic or cardiac shock; coronary insufficiency;
dysrhythmias; organic brain or heart disease; during labor.

Precautions: Elderly or debilitated patients, hypertension, diabetes,
hyperthyroidism, Parkinson’s disease, tuberculosis, asthma, emphysema.

Dosage/Administration: Cardiac arrest: 1 mg IV/IO q 3-5 min. (ET:2-2.5 mg
diluted in 10 ml NS) Peds: 0.01 mg/kg (0.1 ml/kg sol’n) IV/IO every 3-5 minutes
(ET: 0.1 mg/kg of 0.1 ml/kg sol’n) Allergic reactions: 0.3-0.5 mg SQ/IM q 5-15
min.prn or 0.5 mg IV if subcutaneous dose ineffective or severe reaction. Ped:
0.01 mg/kg SQ q 10-15 min. or 0.01 mg/kg IV/IO if SQ dose ineffective or
reaction severe. Symptomatic bradycardia or profound hypotension: 2-10
mcg/min IV infusion, titrate to response. Post-ROSC hypotemsion refractory to
crystalloid bolus 0.1-0.5 mcg/kg/min. Typical autoinjector doses are 0.15 mg and
0.3 mg IM.

Special Considerations: Use with extreme caution in ischemic heart disease.
May nebulize 3mg 1:1000 epinephrine or racemic epinephrine. As of May 1,
2016, ratio expressions of epinephrine concentrations are prohibited on drug labels,
but are still residually used by providers. 1:1,000 1 mg/mL and 1:10,000  0.1
mg/mL

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20
Q

Etomidate

A

Trade Name(s): Amidate®

Class: Hypnotic

Description: Etomidate is an ultra-short-acting nonbarbiturate hypnotic with no
analgesic effects and limited cardiovascular and respiratory effects.

Indication(s): Induce sedation for intubation or as part of a medication “cocktail”
for sedation in rapid sequence intubation.

Contraindication(s): Hypersensitivity

Precautions: Marked hypotension, severe asthma, severe cardiovascular disease
and septic shock.
Dosage/Administration: 0.1-0.6 mg/kg IV over 15-30 seconds with a maximum
dose of 100 mg.Peds: 0.2-0.4 mg/kg over 30-60 seconds with a maximum dose of
20 mg.

Special Considerations: Has an onset of < 1 minute and has a duration of 5-10
minutes; no analgesic properties; masseter muscle spasm if given rapidly

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21
Q

Fentanyl Citrate

A

Trade Name(s): Sublimaze®

Class: Synthetic Opioid Analgesic

Description: Fentanyl is a potent synthetic narcotic/analgesic similar to morphine
and meperidine but with a more rapid and less-prolonged action.

Indication(s): Anesthesia adjunct for endotracheal intubation and to control
moderate to severe pain.

Contraindication(s): MAO inhibitors with 14 days, myasthenia gravis.

Precautions: Increased ICP, elderly, debilitated, COPD, respiratory problems and
hepatic and/or renal insufficiency.

Dosage/Administration: 25-100 mcg slow IV push over 2-3 mins or 3mcg/kg for
use in RSI. Peds: 2mcg/kg slow IV push or IM.

Special Considerations: Rapid injection will result in increased incidence of side
effects up to and including respiratory arrest. 100 times more potent than
Morphine

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22
Q

Flumazenil

A

Trade Name(s): Romazicon®

Class: Benzodiazepine Antagonist

Description: Flumazenil is a benzodiazepine antogonist used to reverse the
sedative, recall and psychomotor effects of diazepam, midazolam and other
bezodiazepines.

Indication(s): Respiratory depression secondary to benzodiazepine overdose

Contraindication(s): Contraindicated in patients hypersensitive to drug or
benzodiazepines, patients who show evidence of serious tricyclic antidepressant
overdose, and patients who received a benzodiazepine to treat a potentially lifethreatening condition such as status epilepticus.

Precautions: Hepatic or renal impairment, alcoholism, hypotension, bradycardia,
heart block, severe CAD, diabetes, hyperglycemia and respiratory depression.

Dosage/Administration:1st dose: 0.2 mg IV over 15 seconds 2nd dose:0.3 mg IV
over 30 seconds, if no adequate response 3rd dose 0.5 mg over 30 seconds. If no
adequate response, repeat once every minute until adequate response or a total of 3
mg is given.

Special Considerations: May induce seizures by reversing benzodiazepine
effects.

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23
Q

Furosemide

A

Trade Name(s): Lasix®

Class: Loop Diuretic

Description: Potent diuretic and antihypertensive that inhibits reabsorption of
sodium and chloride at the distal and proximal tubules and the loop of Henle.
Causes increased urine output. Vasodilatory effects.
Indication(s): Congestive heart failure and pulmonary edema.

Contraindication(s): Hypersensitivity to furosemide or the sulfonamides, fluid
and electrolyte depletion states, hepatic coma, pregnancy (except in lifethreatening circumstances).

Precautions: Infants, elderly, hepatic impairment, nephrotic syndrome,
cardiogenic shock associated with acute MI, gout, patients receiving digitalis or
potassium-depleting steroids.

Dosage/Administration: 0.5-1 mg/kg slow IV push over 1-2 minutes. Standard
Dose 20mg.

Special Considerations: When medication is pushed too quickly patients can
experience tinnitis or transient deafness. It is packaged in amber glass to protect it
from light.Vasodilatory effect within five minutes and diuretic effects within 30 minutes.

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24
Q

Glucagon

A

Trade Name(s): Gluca-Gen®

Class: Hormone/HyperglycemicAgent

Description: Glucagon is a protein secreted by pancreatic cells that causes a
breakdown of glycogen stores into glucose and inhibits the synthesis of glycogen
from glucose.

Indication(s): Hypoglycemia without IV access, reversal of beta-blocker and
calcium channel blocker overdose and management of esophageal food bolus
obstruction.

Contraindication(s): Hypersensitivity to glucagon or protein compounds.

Precautions: Cardiovascular or renal impairment.

Dosage/Administration: Hypoglycemia:1 mg IM/SQ repeat every 5-20 minutes
Peds: 0.03 mg/kg IM/SQ Beta-blocker/Calcium channel blocker overdose:3-10
mg slow IV push over 3-5 minutes. Food bolus: 1-2 mg IV push
Special Considerations: Effective only if there are sufficient stores of glycogen
in the liver

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25
Q

Haloperidol Lactate

A

Trade Name(s): Haldol®

Class: Antipsychotic

Description: Haloperidol is believed to block dopamine receptors in the brain
associated with mood and behavior, it is also a potent antiemetic.

Indication(s): Acute psychosis

Contraindication(s): Parkinson’s disease, seizure disorders, coma, alcohol
depression, CNS depression, thyrotoxicosis and use with other sedatives.

Precautions: Elderly or debilitated patients, urinary retention, glaucoma, severe
cardiovascular disease and anticonvulsant, anticoagulant or lithium therapy, prior
dystonic reactions.
Dosage/Administration: 2-10 mgIM Peds: <3 years 0.015-0.15 mg/kg/day PO or
in 2-3 divided doses.

Special Considerations: It impairs temperature regulation. May cause akathesia,
dystonia, and neuroleptic malignant syndrome (NMS)

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26
Q

Heparin Sodium

A

Trade Name(s): Heparin

Class:Anticoagulant

Description: Heparin is a rapid-onset anticoagulant, enhancing the effects of
antithrombin III and blocking the conversin of prothrombin and fibrinogen to
fibrin.

Indication(s): Prevention of thrombus formation in hypercoaguable conditions (ie
AMI, DVT, PE)

Contraindication(s): Hypersensitivity, active bleeding or bleeding tendencies,
recent eye, brain or spinal surgery and shock.

Precautions: Bleeding
Dosage/Administration: 60 IU/kg maximum bolus of 4,000 IU.

Special Considerations: Should be used with caution with any clinical state in
which there is an increase risk of bleeding (i.e. gi bleed, post-op). Also used in
hospital for initial treatment of new onset atrial fibrillation, deep vein thrombus
and pulmonary embolism.

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27
Q

Hydrocortisone sodium succinate

A

Trade Name(s): Solu-Cortef®

Class: Glucocorticoid

Description: Short-acting synthetic steroid used for its anti-inflammatory action
and as a replacement therapy in adrenocortical insufficiency.

Indication(s): Emergent allergic conditions in asthma, anaphylaxis, transfusion
reactions; adrenocortical insufficiency; cerebral edema; and others.

Contraindication(s): Systemic fungal infections and patients with known
hypersensitivity to the product. IM corticosteroid preparations are contraindicated
for idiopathic thrombocytopenic purpura.

Precautions: There may be decreased resistance and inability to localize infection
associated with use alone or in combination with other immunosuppressive agents.

Dosage/Administration: Given IV or IM. First, reconstitute for injection from
powder with bacteriostatic water or saline (up to 2 mL/250 mg). For IV infusion,
this reconstituted solution can be added to a bag of D5W or NS for a solution
concentration up to 1 mg/mL. Initial dose is 100-500 mg over 30 seconds to 10
minutes.

Special Considerations: Because of possible physical incompatibilities, should
not be diluted or mixed with other solutions.

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27
Q

Ipatropium Bromide

A

Trade Name(s): Atrovent®

Class: Anticholinergic, Bronchodilator

Description: Ipratropium Bromide is a bronchodilator used in the treatment of
respiratory emergencies that causes bronchial dilatition and dries respiratory tract
secretions by blocking acetylcholine receptors.

Indication(s): Bronchospasm associated with asthma, COPD and inhaled irritants.

Contraindication(s): Hypersensitivity to atropine or its derivatives or a as a
primary treatment for acute bronchospasm.

Precautions: Elderly, patients with cardiovascular disease or hypertension and
those with peanut allergy.

Dosage/Administration: 500 mcg in 2.5-3 ml NS via nebulizer or 2 sprays from a
metered dose inhaler. Peds: 125-250 mcg in 2.5-3 mL NS via nebulizer, or 1-2
sprays of a metered dose inhaler.

Special Considerations: Some providers have concerns to hypersensitivity to
peanuts, but with inhalation therapies not a concern.

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27
Q

Hydroxocobalamin

A

Trade Name(s): Cyanokit®

Class: Vitamin, Antidote

Description: Hydroxocobalamin (vitamin B12a) is a precursor to cyanocobalamin
(vitamin B12). In the presence of cyanide, each hydroxocobalamin molecule can
bind one cyanide ion, forming cyanocobalamin, which is then excreted in the urine.

Indication(s): IV for known or suspected cyanide
poisoning; IM for pernicious anemia or vitamin B12
deficiency.

Contraindication(s): IV – None in setting of cyanide
poisoning. IM – Hypersensitivity to drug or other
ingredients.

Precautions: Hypertension may occur with infusion
which subsides within a few hours.

Dosage/Administration: For cyanide poisoning, 5 g IV
as initial single infusion; may repeat a second 5 g dose
depending on the severity and response. Maximum
cumulative dose: 10 g.

Special Considerations: Fire victims may present with
both cyanide and carbon monoxide poisoning. In this
scenario, hydroxocobalamin is the agent of choice for
cyanide intoxication since the traditional cyanide
antidote that contains sodium nitrite produces
methemoglobinemia and may worsen tissue hypoxia.
Hydroxocobalamin can discolor the skin and exudates,
complicating the assessment of burn severity.

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27
Q

Isoetharine

A

Trade Name(s): Bronkosol®. Bronkometer®

Class: Sympathomimetic, Bronchodilator, Beta2Agonist

Description: Isoetharine is a synthetic sympathomimetic with rapid onset and
prolonged duration that relaxes the bronchial smooth muscles, decreasing airway
resistance and helping clear secretions.

Indication(s): Bronchospasm associated with asthma and COPD.

Contraindication(s): Hypersensitvity to or use of sympathomimetic amines, preexisting tachydysrhythmias or allergy to sodium disulfite agents.

Precautions: Elderly, hypertension, acute coronary artery disease, CHF,
hyperthyroidism, diabetes, tuberculosis or seizures.

Dosage/Administration: 1-2 sprays via metered dose inhaler or 0.5 mL in 2-3 mL
NS via nebulizer. Peds: 0.01 mL/kg of 1% solution (max 0.5 mL) diluted in 2-3
mL saline via nebulizer.
Special Considerations: Multiple Doses can cause paradoxical
bronchoconstriction

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27
Q

Insulin

A

Trade Name(s): Humulin®, NovoLog®, Novolin®

Class: Hormone/Antihypoglycemic

Description: Insulin is a naturally occurring protein that promotes the uptake of
glucose by the cells.

Indication(s): Hyperglycemia, diabetic ketoacidosis and hyperkalemia.

Contraindication(s): Hypersensitivity and hypoglycemia.

Precautions: Administration of excessive dose may induce hypoglycemia.
Glucose should be available.

Dosage/Administration:5-10 units IV/IM/SQ Peds: 2-4 units IV/IM/SQ.

Special Considerations: Regular insulin is the only insulin that can be
administered intravenously

27
Q

Ketamine

A

Trade Name(s): Ketalar®

Class: Dissociative Anesthetic, Hypnotic, Analgesic,Sedative

Description: Ketamine is a nonbarbiturate anesthetic/analgesic that produces a
cataleptic-like state in which the patient is dissociated from the surrounding
environment by direct action on the cortex and limbic system. Dissociative
anesthetic related to PCP. Has sedative, amnesic and analgesic properties. Causes
bronchodilation increased airway secreations.

Indication(s): Induction agent for rapid sequence intubation.

Contraindication(s): Hypersentivity to the drug, uncontrolled HTN, and any
disorder with potential increase in ICP.

Precautions: Hallucinations and violent behavior can occur particularly during
emergence. Head injuries as it may precipitate an increase in BP/HR (concerning
only if already very elevated).

Dosage/Administration: 0.5-2 mg/kg slow IV push over 60 seconds, 0.5-
13mg/kg IM once. Peds:0.5-2 mg/kg slow IV push

Special Considerations: It has good brochodilatory effects which make a good
induction agent for patients with asthma and COPD. Can cause laryngospasm.

27
Q

Ipecac

A

Trade Name(s): Ipecac

Class: Emetic/Antidote

Description: Ipecac syrup is a gastric irritant and acts on the emetic centers of the
medulla to induce vomiting.

Indication(s): Poisoning and overdose.

Contraindication(s): Reduced level of consciousness, corrosive ingestion,
petroleum distillate ingestion, alkali ingestion and anitemetic ingestion (especially
phenothiazine).

Precautions: Monitor the airway closely and have suction ready. Administer
activated charcoal only after emesis. Use with caution in patients with heart
disease.

Dosage/Administration: 30 ml PO, followed by 1-2 glasses of water, repeat after
20 minutes as needed. Peds: <I year 5-10 ml PO followed by 1-2 glasses of water,
>1-12 years 15 ml PO followed by 1-2 glasses of water, repeat in 20 minutes as
need.

Special Considerations: Emesis usually occurs within 5-10 minutes. Duration is
20-25 minutes. Have patient sit upright with head forward before administering
dose and for 30 min or more after administration. Do not give this drug without
expert consultation (e.g., Poison Control). It often delays the administration of
actual toxin antidotes and increases aspiration risk

27
Q

Isoproterenol

A

Trade Name(s): Isuprel®

Class: Synthetic Sympathomimetic Amine (pure Beta 1 & 2).

Description: Isoproterenol affects the heart by increasing inotropic and
chronotropic activity. In addition, isoproterenol causes arterial and bronchial
dilation and is sometimes administered via aerosolization as a bronchodilator to
treat bronchial asthma and bronch

Indication(s): Hemodynamically stable bradycardias that are resistant to atropine.
Heart blocks with palpable pulse. Management of torsades de pointes

Contraindication(s): Ventricular tachycardia , hypotension , ischemic heart
disease and cardiac arrest .

Precautions: Use with caution in myocardial infarction or cardiogenic shock as it
will increase ischemia and arrythimias.

Dosage/Administration: Dilute 1 mg in 500 ml of D5W (2 mcg/ml); infuse at 2-
10 mcg/min or until the desired heart rate is obtained. Ped: 0.05-1.5 mcg/kg/min
IV infusion, titrated to patient response.

Special Considerations: Will be inactivated by alkaline solutions

27
Q

Lactated Ringer’s (LR)

A

Trade Name(s): Hartmann’s solution, Ringer’s injection, Ringer’s lactate (RL)

Class: Electrolyte, irrigant
Description: Source of electrolytes and water

Indication(s): Intravascular volume supplementation or replacement

Contraindication(s): Hypersensitivity to sodium lactate or any component of the
formulation; concomitant use with ceftriaxone in neonates.

Precautions: Administer with extreme caution to patients with, or at risk for,
alkalosis, hypervolemia, overhydration, edema, or conditions that may cause
sodium and/or fluid overload, or acid-base imbalance.

Dosage/Administration: Typical 5-30 mL/kg IV, but volume, rate, and duration
are to be individualized and dependent upon the indication for patient
characteristics, concomitant treatment, and clinical condition.
Special Considerations: Lactate is metabolized to bicarbonate and may worsen
metabolic alkalosis.

27
Q

Labetalol

A

Trade Name(s): Trandate®, Normodyne®

Class: Beta Blocker

Description: Labetalol is a beta blocker with some alpha blocker characteristics.
It induces vasodilation, reduses peripheral vascular resistance and lowers blood
pressure.

Indication(s): Acute hypertensive crisis. Premedication in RSI.

Contraindication(s): Asthma, CHF, 2nd-and 3rd-degree heart block, severe
bradycardia and cardiogenic shock.

Precautions: COPD, heart failure, hepatic impairment, diabetes and peripheral
vascular disease.
Dosage/Administration:10 mg slow IVP, then 20-40 mg q 10 mins as needed, up
to 150 mg OR 10 mg bolus, then continuous drip of 2-8 mg/min Peds:0.2-1 mg/kg
IV q10min prn max 20 mg/dose

Special Considerations: Patient should be kept supine for 3 hours following
administration.

27
Q

Ketorolac tromethamine

A

Trade Name(s): Toradol®

Class: Nonsteroidal anti-inflammatory drug (NSAID)

Description: Analgesic

Indication(s): Short-term management of moderately severe acute pain that
requires analgesia at the opioid level.

Contraindication(s): Active or history of peptic ulcer disease, recent GI bleeding
or perforation; renal impairment; suspected or confirmed cerebrovascular bleeding,
patients with hemorrhagic diathesis, incomplete hemostasis and those at high risk
of bleeding; patients currently receiving aspirin; pregnancy; prophylactic
procedural analgesia.

Precautions: Use cautiously in impaired hepatic function or liver disease, aspirin sensitive asthma, and coagulation disorders or anticoagulant use. The safety and
effectiveness of single doses IV/IM have been established in pediatric patients
between the ages of 2 and 16 years, but not below the age of 2 years.

Dosage/Administration: Single Dose: Adults < 65 y/o: 60 mg IM or 30 mg IV;
use half dose if age ≥ 65 y/o, remal impairment, and/or weight < 50 kg. Children
2-16 y/o: 1 mg/kg IM < 30 mg, 0.5 mg/kg IV < 15 mg.

Special Considerations: It is important to report the initial IV/IM dose during
handoff for downstream management because of the broad range of interactions
and side effects of this drug

28
Q

Lidocaine Hydrochloride

A

Trade Name(s): Xylocaine®, et al
Class: Antiarryrhythmic, Local Anesthetic

Description: Lidocaine is an antiarryrhytmic that suppresses automaticity and
raises stimulation threshold of the ventricles. It also causes sedation and has
anticonvulsant and analgesic effects.

Indication(s): Ventricular arrhythmia and ectopy, pain management with
conscious IO, pharyngeal topical anesthesia for orotracheal intubation,
premedication for airway suctioning or RSI in head trauma to blunt ICP
aggravation.

Contraindication(s): Hypersentivity to amide-type local anesthetics,
supraventricular dysrhymias, Stokes-Adams syndrome, 2nd- and 3rd-degree heart
block and bradycardias.

Precautions: Hepatic or renal impairment, CHF, hypoxia, respiratory depression,
hypovolemia, myasthenia gravis, shock, debilatated patients, elderly patients and
family history of malignant hypothermia.

Dosage/Administration: Antiarrhythmic initial IV/IO dose VF, pVT 1-1.5 mg/kg,
pefusing stable VT or PVCs 0.5-1.5 mg/kg; pediatric 1 mg/kg; via ET 2-2.5 x IV
dose in 5-10 mL NS. Repeat IV at half initial dose q 5-10 min. < 3 mg/kg total.
Follow successful Tx with a maintenance drip of 1-4 mg/min in adults or 20-50
mcg/kg/min in pediatric patients. IO flush analgesia 0.5 mg/kg over 30-60 sec. <
50 mg/dose and < 3 mg/kg within 24 hours. Jelly applied topically for oral
intubation should be limited to 30 mL (600 mg)/24 hr.

Special Considerations: Patients receiving IV lidocaine
require continuous ECG monitoring. Maintenance infusion
should be carefully controlled via pump or micro-drip set < 4
mg/min.; faster infusion greatly increases risk of toxicity,
usually manifest as CNS Sx. Reduce maintenance dose 50% in
patients older than 70 years or with hepatopathy or shock.

29
Q

Lorazepam

A

Trade Name(s): Ativan®

Class: Benzodiazepine, Sedative, anticonvulsant, anxiolytic

Description: Lorazepam is the most potent benzodiazepine available. It has
strong antianxiety, sedative, hypnotic and skeletal muscle relaxant properties, with
a relatively short half-life.

Indication(s): Status epilepticus, sedation for cardiversion, severe anxiety

Contraindication(s): Sensitivity to benzodiazepines, Substance abuse (relative),
Coma (unless seizing), Severe hypotension, shock, preexisting central nervous
system depression

Precautions: Narrow-angle glaucoma, depression or psychosis, coma, shock,
acute alcohol intoxication, renal or hepatic impairment, organic brain syndrome,
myasthenia gravis, GI disorders, elderly, dibilatated or limited pulmonary reserve.

Dosage/Administration: Adult Sedation:1-4 mg IM, 0.05mg/kg IV, Adult
Seizures: 2 mg slow IVP;Ped:0.05-0.20 mg/kg slow IV/IO/IM

Special Considerations: May cause hypotension, respiratory depression and
decreased mental status.

30
Q

Magnesium Sulfate

A

Trade Name(s): Magnesium

Class: Electrolyte, antiarrhythmic, anticonvulsant, smooth muscle relaxant

Description: Magnesium sulfate is an electrolyte that acts as a calcium channel
blocker, acting as a CNS depressant and anticonvulsant. It also depresses the
function of smooth, skeletal and cardiac muscles.

Indication(s): Torsade de Pointes, refractory VF/pulseless VT after Amiodarone
or Lidocaine, eclamptic-seizures due to toxemia of pregnancy, asthma,
hypomagnesaemia, arrhythmias due to digitalis toxicity.

Contraindication(s): heart block, myocardial damage, shock, persistent
hypertension or hypocalcemia.
Precautions: Renal impairment, digitalized patients, other CNS depressants or
neuromuscular blocking agents.

Dosage/Administration: Cardiac Arrest: 1-2 grams IV/IO Ped: 25-50 mg/kg
IV/IO max dose 2 grams. Torsades de Points:1-2 grams diluted in 50-100 mL of
D5W over 5-15 mins. Follow with 0.5-1 gram per hour IV titrated to effect. Ped:
25-50 mg/kg IV/IO (max dose 2 grams) over 15-20 min. Status Asthmaticus:2
grams IV/IO given over 20 mins. Ped: 25-50 mg?kg IV/IO over 15-30 min max
dose 2 grams. Eclampsia:2-4 grams IV given over 3-5 min.

Special Considerations: Eclamptic seizures may occur 4-6 weeks after delivery.
Rapid infusion could cause muscle weakness and loss of reflexes as well as
hypotension. May enhance effects of other centreal nervous system depressants;
may cause flushing or sensation of lose of bowel control for patients. Calcium can
be used as antagonist to magnesium

31
Q

Metaproterenol Sulfate

A

Trade Name(s): Alupent®

Class: Sympathomimetic Bronchodilator, Beta-2 Adrenergic Agonist

Description:
Metaproterenol is a synthetic sympathomimetic amine, similar to
isoproterenol that causes smooth muscle relaxation of the bronchial tree,
decreasing airway resistance, facilitating mucus drainage and increasing vital
capacity.

Indication(s): Brochospasm, as in asthma and COPD.
Contraindication(s): Hypersensitivity to sympathomimetic agents,
tachydysrythmias and hyperthyroidism.
Precautions: Elderly, hypertension, coronary artery disease and diabetes.

Dosage/Administration: 0.65 mg via metered dose inhaler (2 sprays); 0.2-0.3 mL
in 2.5-3 mL NS via nebulizer. Ped: 0.1-0.2 mL/kg (5% solution) in 2.5-3 mL NS
via nebulizer.

Special Considerations: Monitor for hypotension

32
Q

Methyprednisolone Sodium Succinate

A

Trade Name(s): Solu-Medrol®

Class: Corticosteroid
Description: Methylprednisolone is a synthetic adrenal corticosteroid, effective as
an anti-inflammatory and used in the mangement of allergic reactions and in some
cases of shock.

Indication(s): Asthma, severe anaphylaxis, COPD.
Contraindication(s): No major contraindications in the emergency setting.

Precautions: Due to delayed onset only useful for the delayed phase of
anaphylaxis.

Dosage/Administration: Asthma/COPD/anaphylaxis:125-250 mg IV/IM ped: 1-
2 mg/kg dose IV/IM.

Special Considerations: NO LONGER USED for spinal cord injuries (shown to
increase mortality); must reconstitute

33
Q

Metoclopramide

A

Trade Name(s): Reglan®

Class: Antiemetic

Description: Blocks dopamine receptors and (when given in higher doses) also
blocks serotonin receptors in chemoreceptor trigger zone of the CNS; enhances the
response to acetylcholine of tissue in upper GI tract causing enhanced motility and
accelerated gastric emptying without stimulating gastric, biliary, or pancreatic
secretions; increases lower esophageal sphincter tone.

Indication(s): Control or prophylaxis of nausea and vomiting. Used less
commonly off label for hiccups and migraine headaches.

Contraindication(s): Hypersensitivity to drug or ingredients; situations where
stimulation of GI motility may be dangerous, including mechanical GI obstruction,
perforation, or hemorrhage; seizure disorder; history of tardive dyskinesia or
dystonic reaction.

Precautions: Rapid IV administration may be associated with a transient (but
intense) feeling of anxiety and restlessness, followed by drowsiness.

Dosage/Administration: 10 mg or 20 mg as a single IV dose; avoid rapid IV
administration of doses >10 mg.

Special Considerations: Metoclopramide can cause tardive dyskinesia, a serious
movement disorder that is often irreversible with no known treatment. The risk of
developing tardive dyskinesia increases with duration of treatment and total
cumulative dose. Discontinue metoclopramide in patients who develop signs or
symptoms of tardive dyskinesia.

34
Q

Metoprolol Tartrate

A

Trade Name(s): Lopressor®

Class: Beta Blocker(beta-1 selective); antihypertensive, antiarryhtmic

Description: Metoprolol is a beta-adrenergic blocking agent that reduces heart
rate, cardiac output and blood pressure.

Indication(s): AMI (systolic dysfunction), Angina Pectoris, Hypertension with
tachycardia; Second line treatment for tachycardias

Contraindication(s): Cardiogenic shock, sinus bradycardia <45, 2nd- or 3rddegree heart block, PR interval >0.24, cor pulmonale, asthma and COPD.

Precautions: Hypersensivity, hepatic or renal impairment, cardiomegaly, CHF
controlled by digitalis and diuretics, AV conduction defects, thyrotoxicosis,
diabetes and peripheral vascular disease.

Dosage/Administration: 5 mg slow IV q 5 min to a total of 15mg

Special Considerations: In pregnancy metoprolol should be given over 5 min. If
patient has systolic dysfunction metoprolol has been shown to increase mortality.

35
Q

Midazolam Hydrochloride

A

Trade Name(s): Versed®

Class: Benzodiazepine, Sedative/Hypnotic

Description: Midazolam is a short-acting benzodiazepine with CNS depressant,
muscle relaxant, anticonvulsant and anterograde amnestic effects.

Indication(s): Sedation before cardioversion. Seizures. Excited delirium states.

Contraindication(s): Hypersensitivity to benzodiazepines, narrow-angle
glaucoma, shock, coma and acute alchohol intoxication.

Precautions: COPD, renal impairment, CHF and the elderly

Dosage/Administration:1-5 mg IV/IM (usually 5 mg) [0.015mg/kg]. Ped: 0.05-
0.2 mg/kg IV: 0.1-0.15 mg/kg IM

Special Considerations: Provide continuous monitoring of respiratory and
cardiac function. May cause hypotension, respiratory and mental status
depression; can be administered IN

36
Q

Morphine Sulfate

A

Trade Name(s): Morphine, Duramorph®, Roxanol®, MS Contin®

Class: Opiod Analgesic

Description: Morphine sulfate is a potent analgesic and sedative that causes some
vasodilation, reducing venous return and reduced myocardial demand.

Indication(s): Pain (burns, MI etc) and cardiac chest pain refractory to nitrates.

Contraindication(s): Hypersensitivity to opiates, undiagnosed head or abdominal
injury, hypotension or volume depletion, acute bronchial asthma, COPD, severe
respiratory depression, pulmonary edema due to chemical inhalation.

Precautions: Elderly, children, debilitated patients.Inferior (Right ventricular)
MI, sepsis.

Dosage/Administration: MI:2-4 mg IV/IO q 5-15 min. Pain management:2-15
mg IV or 5-20 mg IM/SQ. Ped 0.05-0.1 mg/kg IV or 0.1-0.2 mg/kg IM/SQ.

Special Considerations: Should be readily available to counteract the effects of
morphine; May encounter respiratory and mental depression but not necessarily
hypotension. Localized rash near injection site may develop as a result of
histamine release.

37
Q

Nalbuphine Hydrochloride

A

Trade Name(s): Nubain®

Class: Synthetic OpiodAnalgesic

Description: Nalbuphine is a synthetic narcotic analgesic equivalent to morphine,
though its respiratory depression does not increase with higher doses.

Indication(s): Moderate to severe pain.

Contraindication(s): Hypersensitivity, head injury or undiagnoses abdominal
pain.

Precautions: Impaired respirations, narcotic dependency.
Dosage/Administration: 0.4-2 mg/kg IV/IO/IM (2-2.5 times the dose via ETT),
repeated q 2-3 min as needed up to 10 mg. Ped: 0.1-0.2 mg/kg IV/IO.

Special Considerations: Duration is 3 to 6 hours. The dosage should be reduced
in older patients because the effects are less predictable in this age group. Small
repeated doses are often safer than a single large dose.

38
Q

Nalmefene Hydrochloride

A

Trade Name(s): Revex®

Class: Opioid antagonist
Description: Prevents or reverses the effects of opioids, including respiratory
depression, sedation, and hypotension.

Indication(s): The reversal of natural or synthetic opioid drug effects, usually in
the setting of known or suspected opioid overdose.

Contraindication(s): Hypersensitivity to the product.
Precautions: Side effect profile is similar to naloxone at equivalent doses with
nausea, vomiting, tachycardia, and hypertension uncommon but among the most
likely. Safety and effectiveness in neonates and pediatric patients have not been
established.

Dosage/Administration: Can be administered IV, IM, SQ. The recommended
initial dose for known or suspected opioid overdose in non-opioid dependent
patients is 0.5 mg/70kg followed by a second dose of 1.0 mg/70 kg, 2-5 minutes
later prn. Doses of 0.5-1.0 mg effectively reversed respiratory depression within 2
to 5 minutes in most patients subsequently confirmed to have opioid overdose. A
total dose greater than 1.5 mg did not increase the therapeutic response. Should IV
access be lost or not readily obtainable, a single 1.0 mg IM/SQ dose should be
effective within 5-15 minutes.

Special Considerations: While nalmefene has a longer duration of action than
naloxone in fully reversing doses, recurrence of respiratory depression is possible,
even after adequate initial response to treatment

39
Q

Naloxone Hydrochloride

A

Trade Name(s): Narcan®

Class:Narcotic Antagonist

Description: Naloxone is a pure narcotic antagonist that blocks the effects of both
natural and synthetic narcotics and may reverse respiratory depression.

Indication(s): Narcotic and synthetic narcotic overdose, coma of unknown origin

Contraindication(s): Hypersensitivity to the drug, non-narcotic-induced
respiratory depression.

Precautions: Some newborns may have respiratory dcepression secondary to
maternal opiate abuse/use, use of naloxone may precipitate withdrawal

Dosage/Administration:0.4-2 mg IV/IM (2-2.5 times the dose via ETT) or 0.4-
0.8 mg IM/SQ repeated every 2 min as needed. Max single dose is 2 mg.

Special Considerations: Administer only enough to reverse respiratory
depression. It has a half-life that is shorter than that of most narcotics, hence the
patient may return to the overdose state.

40
Q

Nifedipine

A

Trade Name(s): Procardia®, Adalat®

Class: Calcium Channel Blocker

Description: Nifedipine is a calcium channel blocker that reduces coronary artery
spasm in angina. It also decreases peripheral vascular resistance, blood pressure
and cardiac workload.(Has more peripheral effects compared to Diltiazem)

Indication(s): Severe hypertension and angina.
Contraindication(s): Hypersensitivity to the drug or hypotension.

Precautions: Hypotension and peripheral edema.

Dosage/Administration: One 10-20 mg capsule SL/PO.

Special Considerations: Monitor blood pressure carefully, since it can drop
significantly with nifedipine use.

41
Q

Nitroglycerin

A

Trade Name(s): Nitrostat®, Nitro-Bid®, Tridil®

Class: Nitrate, Vasodilator

Description: Nitroglycerin is a rapid smooth muscle relaxant that reduces
peripheral vascular resistance, blood pressure, venous return and cardiac workload.

Indication(s): Chest pain associated with angina, acute myocardial infarction,
acute pulmonary edema, and hypertension.

Contraindication(s): Hypersensitivity to the drug, tolerance to nitrates, severe
anemia, head trauma, hypotension (<90mmHG), severe bradycardia or
tachycardia, increased ICP, patients taking phosphodiesterase inhibitors (sildenafil
- Viagra, vardenafil - Levitra, tadalafil - Cialis within 48 hours)

Precautions: Right Ventricular Infarction (RVI).
Dosage/Administration:(available in IV form, sublingual tablets, paste, and
aerosol spray) 1 SL tablet (0.4mg) at 5 minute intervals for total of 3 doses, or 1 SL
spray (0.4mg) at 5 minute intervals for total of 3 doses, or ½-1 inch of topicalointment, IV: start infusion at 10mcg/min increasing dose by 10mcg/min every 3
to 5 minutes until pain resolves or systolic BP reaches desired level. Dosage
should NOT exceed 200mcg/min.

Special Considerations: Nitroglycerin is light sensitive and will lose potency
when exposed to the air; May induce headache that is sometime severe.

42
Q

Nitrous oxide

A

Trade Name(s): Nitronox™

Class: General anesthetic

Description: General CNS depressant action; may partially act on opiate receptor
systems to cause mild analgesia; central sympathetic stimulating action supports
blood pressure, systemic vascular resistance, and cardiac output; it does not
depress carbon dioxide drive to breath. Nitronox™ is a blend of 50% nitrous oxide
and 50% oxygen.

Indication(s): Sedation, analgesia, and amnesia

Contraindication(s):
Hypersensitivity; should not be administered without
oxygen

Precautions: Nausea/vomiting may occur after therapy.

Dosage/Administration: Concentrations of (25% to) 50% nitrous oxide with
oxygen by mask. Patients can hold the mask to their face and sedation will cause
them to release the mask, providing for self-regulation of therapy.
Special Considerations: Nitrous oxide increases cerebral blood flow and
intracranial pressure while decreasing hepatic and renal blood flow. Oxygen
should be briefly administered during emergence from prolonged anesthesia with
nitrous oxide to prevent diffusion hypoxia.

43
Q

Norepinephrine Bitartrate

A

Trade Name(s): Levophed®

Class: Sympathomimetic agent, vasopressor

Description: Norepinephrine is a naturally occurring catecholamine that acts on
alpha and beta adrenergic receptor sites. Its potency result in peripheral
vasoconstriction, positive chronotropic and increased inotropic effect with
increased cardiac output.

Indication(s): Hypotensive cardiogenic shock and significant hypotension
(70mm Hg) unresponsive to fluid resuscitation, neurogenic shock.

Contraindication(s): Hypotension due to hypovolemia.

Precautions: Hypertension, hyperthyoidism, sever heart disease, elderly, MAO
inhibitor therapy, patients receiving tricyclic antidepressants, use with caution in
pregnancy, other sympathomimetics, and phosphodiesterase inhibitors may cause
dysrhythmias.

Dosage/Administration:
0.1-0.5 mcg/kg/min IV/IO titrated to response. Ped:
0.1-2 mcg/kg/min titrated to BP (rarely used).

Special Considerations: Monitor blood pressure and heart rate frequently,
extravasation will cause tissue necrosis, poison/drug induced hypotension may
require higher doeses to achieve adequate perfusion.

44
Q

Ondansetron Hydrochloride

A

Trade Name(s): Zofran®

Class: Antiemetic, selective serotinin receptor (5-HT3) antagonist

Description: These receptors are found in the vomiting center of the brain and in
the vagus nerve of the stomach and intestine.

Indication(s): Nausea and vomiting.

Contraindication(s):
Hypersensitivity to the drug.

Precautions: Do not administer faster than 30 seconds, patients with liver disease.

Dosage/Administration: IV or IM; Adult 4-8 mg slow IV over 2 min. Ped 0.1
mg/kg

Special Considerations: Repeat dosing does not provide additional control of nausea and vomiting.

45
Q

Oxygen

A

Trade Name(s): Oxygen

Class: Naturally occurring atmospheric gas

Description: Oxygen is an odorless, colorless, tasteless gas, essential for life.

Indication(s): Hypoxia or hypoxemia suspected, present, or anticipated

Contraindication(s): There are no contraindications to oxygen therapy in the
emergency setting. However, the routine automatic administration without
affirmative indication in acute coronary syndromes is not recommended.

Precautions: COPD and very prolonged administration of high concentrations in
the newborn.

Dosage/Administration: High concentration: 10-15 lpm via NRB Low
concentration: 1-6 lpm via nasal cannula. Ped: same as adult dosages.

Special Considerations: Avoid hyperoxygenation and limit oxygen saturation to 99%. in stroke, acute coronary syndrome, and post-ROSC patients.

45
Q

Oxytocin

A

Trade Name(s): Pitocin®

Class: Pituitary Hormone

Description: Oxytocin is a naturally occurring hormone that causes the uterus to
contract, thereby inducing labor, encouraging delivery of the placenta and
controlling postpartum hemorrhage.

Indication(s): Severe postpartum hemorrhage

Contraindication(s): Hypersensitivity, prior to delivery of fetus or fetuses in the
pre hospital setting.

Precautions: Coma, seizures, anxiety, subarachnoid hemorrhage, hypotension,
dysrhythmias, painful uterine contraction, or uterine rupture

Dosage/Administration: 3-10 units IM after delivery of the placenta. 10-40 units
in 500 mL of D5W or NSS IV titrated to effect.

Special Considerations: Uterine tone, ECG and vital signs should be monitored
during administration.

46
Q

Pancuronium Bromide

A

Trade Name(s): Pavulon®

Class: Nondepolarizing Neuromuscular Blocker, paralytic

Description: Pancuronium is a nondeploarizing neuromuscular blocker that
causes paralysis without bronchospasm or hypotension: it does not cause the
fasciculations associated with polarizing agents.

Indication(s): Induction or maintenance of endotracheal intubation

Contraindication(s): Hypersensitivity to the drug or bromides
Precautions: Debilitated patients, myasthenia gravis, fluid/electrolyte imbalance,
renal impairment.

Dosage/Administration:0.04-0.1 mg/kg IV. Ped same as adult.

Special Considerations: Has no effect on consciousness or pain, don’t mix in
same syringe or give through same needle with barbiturates or other alkaline solutions

47
Q

Phenylephrine

A

Trade Name(s): Neo-Synephrine®

Class: Alpha-adrenergic agonist, vasopressor

Description: Potent alpha-adrenergic agonist producing systemic arterial
vasoconstriction with virtually no beta-adrenergic activity.

Indication(s): Treatment of hypotension, vascular failure in shock. Not
recommended for septic shock, but can be considered for cardiogenic shock
associated with left ventricular outflow tract obstruction (e.g., aortic stenosis).

Contraindication(s): Hypersensitivity to drug or any ingredient, severe
hypertension; ventricular tachycardia.

Precautions: May cause severe bradycardia (likely baroreflex mediated) and
reduced cardiac output due to an increase in cardiac afterload especially in patients
with preexisting cardiac dysfunction. Avoid extravasation; ensure proper needle or
catheter placement prior to and during infusion.
Dosage/Administration: Adult: IV push 100-500 mcg/dose q 10- 15 minutes
prn, IV infusion 0.1-10 mcg/kg/min. Pediatric: IV push 5-20 mcg/dose q 10-15
min. prn < 500 mcg, IV infusion 0.1-0.5 mcg/kg/min.

Special Considerations: Assure adequate intravascular volume prior to IV use in
hypotensive patients

48
Q

Pralidoxime Chloride

A

Trade Name(s): 2-PAM, Protopam®

Class: Cholinesterase reactivator

Description: Reactivates cholinesterase to effectively act as an antidote to
organophosphate and pesticide poisonings. This action allows for destruction of
accumlated acetylcholine at the neurolmuscular junction resulting in reversal of
respiratory paralysis and paralysis of skeletal muscle.

Indication(s): Organophosphate and nerve agent poisoning, anticholinesterase
overdoses.

Contraindication(s): No contraindications if organophosphate and nerve agent
poisoning, anticholinesterase overdoses.

Precautions: May result in tachycardia, laryngospams,
muscle rigidity, or
excited/manic behavior after regaining consciousness.

Dosage/Administration: 1-2 grams over 30 minutes IV. 1-2 grams IM/SQ if IV
unavailable. If 3 sets are given then give 10 mg Valium IM.

Special Considerations: Auto-injectors available: Mark 1 (NAAK) kit consist of two separate injectors and Duodote is a single injector. Both contain 2.1mg of Atropine and 600mg of Pralidoxime Chloride in 2 mL

49
Q

Procainamide Hydrochloride

A

Trade Name(s): Pronestyl®

Class: Antiarrhythmic

Description: Procainamide prolongs ventricular repolarization, slows conduction
and decreases mycardial excitability.

Indication(s): Stable wide complex tachycardias, reentry SVT uncontrolled by
vagal maneuvers or adenosine, atrial fibrillation with rapid rate Wolff-ParkinsonWhite syndrome.

Contraindication(s): Hypersensitivity to procainamide and procaine, myasthenia
gravis, Torsades de pointes, second and third degree heart AV block, digitalis toxicity, tricyclic antidepressant overdose.

Precautions: Hypotension, cardiac enlargement, CHF, AMI, ventricular
dysrythmias from digitalis, hepatic or renal impairment, electrolyte imbalance or
bronchial asthma.

Dosage/Administration: 20 mg/min IV dripto effect to a max of 17 mg/kg, then
1-4 mg/min. Ped: 15 mg/kg IV/IO over 30-60 min.

Special Considerations: Medication should be discontinued when: 1) arrhythmia
is suppressed, 2) hypotension occurs, 3) QRS widens by > 50%, 4) maximum dose
of 17mg/kg is given

49
Q

Propofol

A

Trade Name(s): Diprivan®

Class: Sedative hypnotic, short-acting

Description: produces a rapid and brief state of general anesthesia

Indication(s): anesthesia induction, anesthesia maintenance, sedation for
mechanically ventilated patients

Contraindication(s): hypovolemia, known sensitivity including soybean oil,
peanuts, and eggs

Precautions: Seizure, apnea, dysrhythmias, asystole, hypotension, hypertension,
N/V, involuntary muscle movement, acute renal failure

Dosage/Administration:
Adult Induction dose: 1-3mg/kg IV/IO. Adult
maintenance infusion: 25-75 mcg/kg/min IV/IO. Pediatric Induction: 2.5-
3.5mg/kg IV/IO Pediatric maintenance 125-
300mcg/kg/min IV/IO.

Special Considerations: Onset: <1minute. Duration: as long as infusion is
running. In pediatric patients when used with Fentanyl can cause profound
bradycardias; sedative only

50
Q

Racemic Epinephrine

A

Trade Name(s): microNefrin®, Vaponefrin®

Class: Sympathomimetic

Description: Racemic epinephrine is a variation of epinephrine used only for
inhalation to induce brochodilation and to reduce laryngeal edema and mucus
secretions.

Indication(s): Croup, laryngotracheobronchitis, larygnaledema, bronchial asthma,
prevention of bronchospasms.

Contraindication(s): Hypersensitivity, hypertension, and epiglottitis.

Precautions: May result in tachycardia and other dysrythmias.

Dosage/Administration: 0.25-.075 mL of a 2.5% solution in 2 mL NSS once via nebulizer. Ped: same as adult.

Special Considerations: Patient vital signs and ECG should be closely
monitored

51
Q
A
52
Q

Rocuronium Bromide

A

Trade Name(s): Zemuron®

Class: Nondepolarizing Neuromuscular Blocker

Description: Rocuronium is a nondepolarizing neuromuscular blocker that blocks
nerve impulses to the muscles, resulting in temporary muscle paralysis.

Indication(s): Induction or maintenance of endotracheal intubation

Contraindication(s): Known sensitivity to bromides.

Precautions: Use with caution in heart and liver disease.
Dosage/Administration: 0.6mg -1.2mg mg/kg; DAC: 1-1.5 mg/kg IV/IO

Special Considerations: Has no effect on consciousness or pain, Onset: 1-2
minutes. Duration: 40-120 minutes

52
Q

Sodium Bicarbonate

A

Trade Name(s): Neut®

Class: Alkalizing Agent

Description: Metabolic buffer; Sodium bicarbonate provides vascular bicarbonate
to assist the buffer system in reducing the effects of metabolic acidosis and lactic
acid build up and also used in the treatment of some overdoses.

Indication(s): Aspirin, Tricyclic antidepressant, barbituate overdose, refractory
acidosis and hyperkalemia.

Contraindication(s): Metabolic and respiratory alkalosis, hypokalemia.

Precautions: May cause alkalosis if given in too large a quantity; will NOT help metabolic acidosis unless there is sufficient ventilation

Dosage/Administration: 1 mEq/kg 8.4% IV/IO;<1 month old: 1 mEq/kg IV/IO
4.2% concentration; AHA Recomends: 50mEq for hyperkalemia to avoid
alkalosis.

Special Considerations: May be beneficial in treating metabolic acidosis in prolonged states of cardiac arrest, may deactivate vasopressors, and may
precipitate with calcium chloride.

53
Q

Sodium Chloride

A

Trade Name(s): 0.9% Sodium Chloride, Normal Saline (NS), Hypertonic Saline,
NaCl

Class: Electrolyte, irrigant, lubricant

Description: Isotonic or hypertonic salt solution

Indication(s): Restore or supplement intravascular water/sodium loss, moisten
pulmonary secretions, inhaled nebulized bronchodilator diluent, wound and eye
irrigant, fluid flush to facilitate IV/IO drug administration or confirm patency of
infusion delivery system. Moisten and lubricate flexible airway suction catheters.

Contraindication(s): Hypersensitivity to sodium chloride or any component of
the formulation; hypertonic uterus, hypernatremia, fluid retention

Precautions: Use with caution in hypertension, edema, heart failure, renal
impairment.

Dosage/Administration: Intravascular resuscitation typically 5-30 mL/kg , but
volume, rate, and duration are to be individualized and dependent upon the
indication for patient characteristics, concomitant treatment, and clinical condition.
IV/IO flush 1-10 mL IV push depending on purpose and infusion set-up.

Special Considerations: Irrigant form is for external use only; not for parenteral
use. Broadly compatible with emergency care parenteral medications and blood
administration

53
Q

Sodium Nitrate

A

Trade Name(s): With Sodium thiosulfate: Nithiodote®

Class: Antidote cyanide poisoning adjunct

Description: Sodium nitrite promotes formation of methemoglobin, which
combines with cyanide to form nontoxic cyanomethemoglobin which prevents
toxic effect.

Indication(s): Cyanide Poisoning

Contraindication(s): None in acute cyanide poisoning

Precautions: May cause hypotension, tachycardia, fainting, N/V

Dosage/Administration:Adult 300mg slow IVP over 5 minutes or dilute 300mg in
100mL of NSS and infuse slowly. Pediatrics: 10mg/kg IV/IO over 3-5 minutes

Special Considerations: Potent vasodilator causes significant hypotension if
given too rapidly. Part of cyanide antidote kit which also includes amyl nitrite and sodium thiosulfate

54
Q

Sodium Thiosulfate

A

Trade Name(s): With Sodium nitrate: Nithiodote®

Class: Antidote cyanide poisoning adjunct

Description: Converts cyanide to the less toxic thiocyanate, which is then
excreted in urine

Indication(s): Cyanide Poisoning

Contraindication(s): None in acute cyanide poisoning

Precautions:None
Dosage/Administration: Adult: 12.5 g IV/IO slow push over 10 minutes. Peds:
400 mg/kg IV/IO slow push over 10 minutes.
Special Considerations: This is the third step in the three step treatment preceded
by amyl nitrite and sodium nitrate.

55
Q

Sotalol

A

Trade Name(s): Betapace®

Class: Beta Blocker, antiarrhythmic

Description: Sotalol is a nonselective beta blocker that slows heart rate and
decreases AV conduction and irritablility.

Indication(s): Ventricular and supraventricular dysrhythmias.

Contraindication(s): Hypersensitvity to the drug, bronchial asthma, sinus
bradycardia, 2nd- and 3rd-degree heart block, long QT syndromes, cardiogenic
shock, uncontrolled CHF and COPD.

Precautions: CHF, electrolyte disturbances, recent MI, diabetes, sick sinus
rhythms, and renal impairment.

Dosage/Administration: 1-1.5 mg/kg IV/IO.

Special Considerations: Causes QT interval prolongation which can lead to
Torsades de pointe.

56
Q

Succinylcholine Chloride

A

Trade Name(s): Anectine®

Class: Depolarizing Neuromuscular Blocker

Description: Succinylcholine is an ultra-short-acting depolarizing neuromuscular
blocker.

Indication(s): Induction of endotracheal intubation

Contraindication(s): Hypersensitivity to the drug, family history of malignant
hyperthermia, renal failure, hyperkalemia, burns and crush injuries after 48 hours,
muscular dystrophy, neurolmuscular diseases, penetrating eye injury, narrow-angle
glaucoma. Do not use to maintain paralysis.

Precautions: Severe burn or crush injuries, electrolyte imbalance,
hepatic/cardiac/renal/pulmonary impairment, fractures, spinal cord injury,
dehydration, severe anemia and porphyria. Oxytocin, beta blockers, and
organophosphates may potentiate effects. Diazepam may reduce duration of
action.

Dosage/Administration: 1-2 mg/kg IV/IO Ped: same as adult

Special Considerations: Consider premedication with Atropine in pediatric age
group to combat bradycardia. Premedication with Lidocaine may blunt ICP
increase during intubation. Etomidate, diazepam, and midazolam should be used
in any conscious patient receiving neurolmuscular blocker.

57
Q

Terbutaline Sulfate

A

Trade Name(s): Brethine®, Bricanyl®

Class: Sympathomimetic Agonist, Beta-2 Adrenergic Agonist, Bronchodilator

Description: Selective beta-2 adrenergic receptor agonist that results in relaxation
of smooth muscle of bronchial tree, and peripheral vasculature with minimal
cardiac effects.

Indication(s): Bronchial asthma and bronchospasm in COPD. Tocolytic in
premature labor.

Contraindication(s): Hypersensitivity to the drug, tachyarrythmias.

Precautions: The patient may experience palpitations, anxiety, nausea and/or
dizziness. Use caution with patients that have cardiac and hypertensive histories.
MAOIs may potentiate arrythmias, and beta blockers may antagonize effects.

Dosage/Administration: 2 inhalations with a metered dose inhaler repeated once
after 1 min or 0.25 mg SQ repeated in 15-30 minute with maximum dose of 0.5mg
in a 4 hour period.

Special Considerations: Vital signs and breath sounds must be monitored, patient
should be receiving oxygen before and during administration.

58
Q

Thiamine

A

Trade Name(s): Betaxin®
Class: Vitamin
Description: Thiamine is vitamin B1, which is required for carbohydate
metabolism. It is not manufactured by the body and must be constantly provided
from ingested foods.
Indication(s): Coma of unknown origin, chronic alchoholism with associated
coma and delirium tremens, beri-beri, Wernike encephalopathy
Contraindication(s): None.
Precautions: Known hypersensitivity to the drug.
Dosage/Administration: 50-100 mg slow IV/IM Ped: 10-25 mg IV/IM
Special Considerations: Brain is extremely sensitive to thiamine deficiencies,
administration can cause burning sensation

59
Q

Tranexamic Acid (TXA)

A

Trade Name(s): Cyklokapron®, Lysteda®

Class: Antifibrinolytic agent, hemostatic agent

Description: Favors clot formation by displacing plasminogen from fibrin
resulting in inhibition of fibrinolysis and inhibiting the proteolytic activity of
plasmin that break down clots.

Indication(s): Supplement the control of traumatic, intracranial, and postpartum
hemorrhage.

Contraindication(s): Hypersensitivity to tranexamic acid or any component of
the formulation, active intravascular clotting

Precautions: May cause CNS depression. Use with caution in patients with renal
impairment. Visual defects have been reported.

Dosage/Administration: Load 1 g IV/IO over
10 minutes. May be followed by another 1 g
within and over the next several hours in the
hospital depending on the clinical situation.

Special Considerations: Used short-term for
bleeding associated with dental procedures in
patients with hemophilia or on oral
anticoagulant therapy

60
Q

Vasopressin

A

Trade Name(s): Pitressin®
Class: Hormone/Vasopressor

Description: Vasopressin is a hormone with strong vasopressive and antidiuretic
porperties.

Indication(s): Alternative vasopressor to first or second dose of epinephrine in
cardiac arrest, alternative to epinephrine in asystole/PEA. To increase peripheral
vascular resistance in arrest (CPR) or to control bleeding from esophageal varices.

Contraindication(s): Chronic nephritis with nitrogen retention, ischemic heart
disease, PVCs, advanced arteriosclerosis and 1st stage of labor.

Precautions: Epilepsy, migraine, heart failure, angina, vascular disease, hepatic
impairment, elderly and children.

Dosage/Administration: Arrest: 40 units IV/IO. Ped: 0.4-1 unit/kg IV/IO to a
maximum of 40 units. Esophageal varices: 0.02-0.04 units/min IV drip.

Special Considerations: May increase peripheral vascular resistance and provoke
cardiac ischemia and angina.

61
Q

Vecuronium Bromide

A

Trade Name(s): Norcuron®

Class: Nondepolarizing
Neuromuscular Blocker

Description: Neuromuscular agent with intermediate duration of action that
competes with acetylcholine for receptors at the motor end plate resulting in
neuromuscular blockade with minimal cardiac effects.

Indication(s): Induction or maintenance of endotracheal intubation

Contraindication(s): Hypersensitivity to the drug.

Precautions: Myasthenia gravis, hepatic or renal impairment, fluid and electrolyte
imbalance, malignant hyperthermia.

Dosage/Administration: 0.1-0.2 mg/kg IV/IO; Maintenance dose within 45-60
minutes: 0.8-1.2 mg/kg IV/IO Ped: 0.1-0.3 mg/kg IV/IO; maintenance dose:
0.01-0.05 mg/kg IV/IO.

Special Considerations: Paralytic therapy should be started only after adequate
sedation therapy has been initiated. Ongoing sedation should be maintained and
evaluated periodically. Vecuronium will not stop neuronal seizures, pulse rate and
cardiac out may increase, decrease dose for patients with renal disease.

62
Q

Verapamil Hydrochloride

A

Trade Name(s): Isoptin®, Calan®

Class: Calcium Channel Blocker

Description: Verapamil is a calcium channel blocker that slows AV conduction,
suppresses re-entry dysrhythmias such as PSVT, and slows ventricular responses to
atrial tachydysrhythmias. Verapamil also dilates coronary arteries and reduces
mycardial oxygen demand; actions more cardioactive than peripherally active, has
more negative intotropic and chronotropic effects compared to cardizem

Indication(s): PSVT refractory to Adenosine, atrial flutter and atrial fibrillation
with rapid ventricular response, reentry SVT.

Contraindication(s): Severe hypotension, cardiogenic shock, 2nd- or 3rd-degree
heart block, CHF, Lown-Ganong-Levine syndrome, left ventricular dysfunction,
sinus node disease, accessory AV pathways, wide complex tachycardias and
WPW. It should not be administered to patients taking beta blockers.

Precautions: Antihypertensive may potentiate hypotensive effect, increases serum
concentration of digoxin, Hepatic and renal impairment, MI with coronary artery
occlusion and myocardial stenosis.

Dosage/Administration: 2.5-5 mg IV bolus over 2 min (over 3 minutes in
elderly), then 5-10 mg after 15-30 min to a max of 20 mg. Ped: 0.01-0.02 mg/kg
(over 2 minutes), repeat dose in 30 minutes if not effective (do not use in children
younger than 12 months of age); Ped: Newborn 0.1-0.2 mg/kg (not to exceed
2mg), age 1-15 0.1-0.3mg/kg (not to exceed 5mg).

Special Considerations: Beta-adrenergic blockers may have additive negative
inotropic and chronotropic effects, AV block or asystole may occur because of
slowed atrioventricular conduction.

63
Q
A