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63 Cards in this Set

  • Front
  • Back
BRAND NAME

diphenhydramine HCl
Benadryl
CLASS

diphenhydramine HCl
antihistamine, anticholinergic
MECHANISM OF ACTION

diphenhydramine HCl
Blocks cellular histamine receptors, but does not prevent histamine release; results in decreased capillary permeability and decreased vasodilation, as well as prevention of bronchospasm.

Has some anticholinergic effects.
INDICATIONS

diphenhydramine HCl
Anaphylaxis (2nd line)

Phenothiazine reactions (extrapyramidal symptoms)

Antiemetic
CONTRAINDICATIONS

diphenhydramine HCl
Known hypersensitivity to diphenhydramine or drugs of similar chemical structure.

Newborn or premature infants; nursing mothers.

Considerable caution in patients with glaucoma, acute narrow angle; stenosing or obstructive diseases of the GI tract; bronchial asthma; hyperthyroidism; cardiovascular disease or HTN; age greater than 60 years (all relative benefit vs. risk).
ADVERSE REACTIONS

diphenhydramine HCl
CV: Hypotension, palpitations, arrhythmias, hemolytic anemia.

RESP: Anaphylaxis, thickening of bronchial secretions, tightness in chest, wheezing, nasal stuffiness.

CNS: Sedation, visual disturbances, seizures.

GU/GI: Urinary frequency or retention; vomiting.

CHILDREN: In children, may cause paradoxical CNS excitation, seizures, palpitations, thickening of bronchial secretions.
ADULT DOSAGE

diphenhydramine HCl
ANAPHYLAXIS: 25-50 mg slow IV push or deep IM.

EXTRAPYRAMIDAL SYMPTOMS AND ANTIEMETIC: 10-50 mg IV or deep IM, dose individualized according to the needs and pt response.
PEDIATRIC DOSAGE

diphenhydramine HCl
1.0-1.25 mg/kg slow IV push; may also be given deep IM.
BONUS

diphenhydramine HCl
Not used in newborn or premature infants; used in pregnancy only if clearly needed.

In anaphylaxis, used as a 2nd line treatment after epi and steroids.
BRAND NAME

albuterol sulfate
Proventil, Ventolin
CLASS

albuterol sulfate
sympathomimetic, bronchodilator
MECHANISM OF ACTION

albuterol sulfate
β antagonist (primarily β2); relaxes bronchial smooth muscle, resulting in bronchodilation; also relaxes vascular and uterine smooth muscle; decreases airway resistance.
INDICATIONS

albuterol sulfate
Treatment of bronchospasm
CONTRAINDICATIONS

albuterol sulfate
Synergistic with other sympathomimetics.

Use caution in pts with diabetes, hyperthyroidism, and cerebrovascular disease.
ADVERSE REACTIONS

albuterol sulfate
CV: Dysrhythmias, tachycardia (with excessive use), peripheral vasodilation.

RESP: Bronchospasm (rare paradoxical with excessive use).

CNS: Tremors, nervousness

GI: N/V

ENDOCRINE: Hyperglycemia
ADULT DOSAGE

albuterol sulfate
Give 2.5 mg of premixed solution for inhalation (0.083%) via SVN, or in-line with a ventilatory device. Repeat doses per medical control.
PEDIATRIC DOSAGE

albuterol sulfate
For children < 40 lbs., administer half of 0.083% premixed solution; add 1-1.5 mL NS to make 2.5-3 mL treatment administered via SVN, O2 mask or in-line with a ventilatory device. Repeat doses per medical control.
BONUS

albuterol sulfate
ROUTES OF ADMINISTRATION

Nebulized, mouth piece or in-line via mask

Inhaler, patients own

In-line with ET tube/nasotracheal tube

SPECIAL NOTES

Must be sulfite-free
BRAND NAME

dexamethasone sodium phosphate
Decadron
CLASS

dexamethasone sodium phosphate
synthetic adrenocorticoid/glucocorticoid with a predominance of glucocorticoid action, anti-inflammatory.
MECHANISM OF ACTION

dexamethasone sodium phosphate
Improves lung function and myocardial performance

Decrease in pulmonary edema

Relaxation of bronchospasm
INDICATIONS

dexamethasone sodium phosphate
Reactive airway disease: Acute exacerbation of bronchial asthma.

Anaphylaxis.

Cerebral edema (non-traumatic)
CONTRAINDICATIONS

dexamethasone sodium phosphate
Systemic fungal infections.

Hypersensitivity to any component of dexamethasone, including sulfites.

Preterm infants.
ADVERSE REACTIONS

dexamethasone sodium phosphate
Sodium retention, fluid retention, potassium loss, hypokalemic alkalosis, HTN, convulsions, hyperglycemia, myocardial rupture following recent MI.
ADULT DOSAGE

dexamethasone sodium phosphate
REACTIVE AIRWAY DISEASE, ANAPHYLAXIS: 8-24 mg IV/IO or deep IM.

CEREBRAL EDEMA: 1-5 mg/kg IV/IO or deep IM.
PEDIATRIC DOSAGE

dexamethasone sodium phosphate
REACTIVE AIRWAY DISEASE, ANAPHYLAXIS: 0.25-0.5 mg/kg IV/IO

CEREBRAL EDEMA: 0.5-1.5 mg/kg IV/IO
BONUS

dexamethasone sodium phosphate
Dexamethasone is not compatible with benadryl or versed in IV tubing.
BRAND NAME

methylprednisolone sodium succinate
Solu-Medrol
CLASS

methylprednisolone sodium succinate
corticosteroid, glucocorticoid, steroid, anti-inflammatory
MECHANISM OF ACTION

methylprednisolone sodium succinate
Enters target cells and causes many complex reactions that are responsible for its anti-inflammatory and immunosuppressive effects; thought to stabilize cellular and intracellular membranes.
INDICATIONS

methylprednisolone sodium succinate
Reactive airway disease: Acute exacerbation of emphysema, chronic bronchitis, asthma

Anaphylaxis

Burns potentially involving the airway
CONTRAINDICATIONS

methylprednisolone sodium succinate
Preterm infants
ADVERSE REACTIONS

methylprednisolone sodium succinate
None from a single dose.
ADULT DOSAGE

methylprednisolone sodium succinate
REACTIVE AIRWAY DISEASE, ANAPHYLAXIS, BURNS POTENTIALLY INVOLVING THE AIRWAY: Usual dose 125 mg slow IV bolus (much larger doses can be used).
PEDIATRIC DOSAGE

methylprednisolone sodium succinate
REACTIVE AIRWAY DISEASE, ANAPHYLAXIS, BURNS POTENTIALLY INVOLVING THE AIRWAY: 2-4 mg/kg slow IV bolus.
BONUS

methylprednisolone sodium succinate
ADULT DOSAGE CONTINUED - ACUTE SPINAL CORD TRAUMA: Should be within 6 hours of insult and pt meets criteria, inital bolus of 30 mg/kg IV administered over 15 minutes; bolus followed by a 45 min rest period, then a 23-hour continuous infusion of 5.4 mg/kg/hr.

SPECIAL NOTES: Use for spinal cord trauma is limited to prehospital providers that have completed a special training curriculum in accordance with their medical control authorities. PROPER administration of methylprednisolone for spinal cord trauma is imperative.

INFUSIONS: An infusion pump is required for continuous infusions of corticosteroids during inter-facility transports; a minimum of microdrip tubing is required for field use if administering loading dose therapy for spinal cord trauma.
BRAND NAME

phenylephrine nasal spray 0.5%
Neo-synephrine Nasal Spray 0.5%
CLASS

phenylephrine nasal spray 0.5%
topical vasoconstrictor
MECHANISM OF ACTION

phenylephrine nasal spray 0.5%
Stimulates α-receptors in the blood vessels of the nasal mucosa which causes their constriction and thereby decreases the risk of nasal bleeding.
INDICATIONS

phenylephrine nasal spray 0.5%
Facilitation of nasotracheal intubation.
CONTRAINDICATIONS

phenylephrine nasal spray 0.5%
Known allergy to medication.
ADVERSE REACTIONS

phenylephrine nasal spray 0.5%
(rare with single dose, rarely absorbed systemically from nasal instillation)

CV: HTN, palpitations

CNS: Tremors
ADULT DOSAGE

phenylephrine nasal spray 0.5%
2-4 sprays in each nostril before attempting tube insertion.
PEDIATRIC DOSAGE

phenylephrine nasal spray 0.5%
None.
BONUS

phenylephrine nasal spray 0.5%
SPECIAL NOTES:

Single patient use only.

Air or strong light causes potency loss; do not use solution if brown in color or precipitate is in the bottle.
BRAND NAME

furosemide
Lasix
CLASS

furosemide
Loop diuretic
MECHANISM OF ACTION

furosemide
PHARMACOLOGIC: Inhibits electrolyte reabsorption in the ascending Loop of Henle. Promotes excretion of sodium, potassium and chloride. Vasodilation increases venous capacitance and decreases afterload.

CLINICAL: Diuresis.
INDICATIONS

furosemide
Pulmonary edema

CHF
CONTRAINDICATIONS

furosemide
Anuria (relative)

Hypovolemia

Hypotension
ADVERSE REACTIONS

furosemide
May exacerbate hypovolemia

Hyperglycemia (due to hemoconcentration)

Hypokalemia

May decrease the response to pressors
ADULT DOSAGE

furosemide
ON ORAL FUROSEMIDE THERAPY: Consider initial dose of 2 times daily oral dose; if no effect in 20 min may double inital dose.

NOT ON ORAL FUROSEMIDE THERAPY: 0.5-1 mg/kg to a maximum of 2 mg/kg (usually 20-40 mg) IV/IO slowly.
PEDIATRIC DOSAGE

furosemide
1 mg/kg IV/IO slowly
BONUS

furosemide
Ototoxicity and resulting deafness can occur.

Since furosemide is a sulfonamide derivative, it may induce allergic reactions in pts with sensitivity to sulfonamides (sulfa drugs).
BRAND NAME

ipratropium bromide
Atrovent
CLASS

ipratropium bromide
anticholinergic, bronchodilator
MECHANISM OF ACTION

ipratropium bromide
Anticholinergic (parasympatholytic) agent appears to inhibit vagally-mediated reflexes by antagonizing the action of acetylcholine, the transmitter released from the vagal nerve.
INDICATIONS

ipratropium bromide
Treatment of bronchospasm associated with COPD (emphysema and chronic bronchitis).

To be used either alone or in combination with Albuterol.
CONTRAINDICATIONS

ipratropium bromide
Ipratropium bromide is contraindicated in known or suspected cases of hypersensitivity to ipratropium bromide or to atropine and its derivates.

PRECAUTION: Should be used with caution in pts with narrow angle glaucoma.
ADVERSE REACTIONS

ipratropium bromide
RESP: Coughing, sputum increased

CNS: Dizziness, insomnia, tremors, nervousness

GI: Nausea
ADULT DOSAGE

ipratropium bromide
Give 500 mcg in 2.5 mL NS (1 unit dose vial) via SVN or in-line with a ventilatory device. Repeat according to medical control preference.

May mix one unit dose vial of ipratropium bromide with one unit dose vial of albuterol.
PEDIATRIC DOSAGE

ipratropium bromide
Not used pre-hospital for peds.
BONUS

ipratropium bromide
Anticholinergics produce preferential dilation of the larger central airways, in contrast to beta agonists, which affect the peripheral airways.

May be more effective used in combination with beta agonists.

Should be kept out of light in a foil pouch and avoid excessive humidity.