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40 Cards in this Set

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Albuterol class
sympathpometic bronchodilator
Albuterol mechanism of action
sendative basta-2 agonist that stimulates adrenic receptors of the sympathomimetic nervous system resultin in smotth muscle relaxation in the bronchial tree and peripheral vasculature
Albuterol Indication
treatment of bronchospasm in patients with reversable obstructive airway disease (COPD/asthma) prevention of exercise induced bronchospasm
Albuterol contraindications
known priop hypersensitivity reactions to albuterol. tachycardia arrhythmias, especially those caused by digitalis. synergistic with other sympathomimetics
Albuterol adverse reactions
often dose-related and include restlessness, tremors, dizziness, palpitations, tachycardia, nervousness, peripheral vasodilation, nausea, vommiting, hyperglycemia, increased bp, paradoxial bronchospasm
Albuterol Drug interactions
tricylic antidepressants may potentiate vasculature effects. Beta blockers are antagonistic. May potentiate hypokalemia caused by diuretics
Albuterol adult dose
2.5mg dilute .5mL of .5% solution for inhalation with 2.5mL NS in nebulizer admin over 10 - 15 min. MDI: 1-2 inhalations of .01-.03mL (.05-.15mg/kg/dose) rpt 3x in 20min
Albuterol duration of action
onset 5-10 min fo rpeak 30min to 2 hours 3-4 hours
dextrose 50%(D50) class
carbohydrate, hypotonic solution
dextrose 50%(D50) mechanism of action
rapidly increases serum glucose levels. short-term osmotic diuretics
dextrose 50%(D50) indications
hyperglycemia, altered level of consciousness, coma of unknown etiology, seizure of unknown etiology, status epilepticus.
dextrose 50%(D50) contraindications
intracranial hemorrhage
dextrose 50%(D50) adverse reactions
extravastion leads to tissue necrosis. warmth, pain, burning, thrombophlebitis, rhabdomyolsis, hyperglycemia
dextrose 50%(D50) drug interactrions
sodium bicard, coumadin
dextrose 50%(D50) dosage
adult 12.5 - 25g slow IV
dextrose 50%(D50) duration
onset: hours peak: 8-12 duration: 24-72
glucagon class
hyperglycemic agent pancreatic hormone, insulin antagonist
glucagon mechanism of action
increase blood glucose level by stimulating glycogenesis. unknown menchanism of stablizing cardiac rhythm ion beta blocker overdose. Minimal positive inotropic and chronotropic response. decreases gastrointestinal motility and secretions
glucagon indications
altered level of consciousness when hypoglycemia is suspected. May be used as inotropic agent in beta blocker overdose.
glucagon contraindications
hyperglycemia, hypersensitivity
glucagon adverse reactions
nausea, vomiting, tachycardia, hypertension
glucagon drug interactions
incompatible in solution with most other substances. no signigicant drug interactions with other emergency medications.
glucagon doseage
adult: .5-1.0 mg IM repeat 7-10 min calcium channel blocker or beta blocker OD : 3mg initially followed 3mg/hr infusion
glucagon duration of action
onset: 1min peak 30min duration: variable (9-17 normal)
Phenergan (promethazine) class
antihistamine
Phenergan (promethazine) mechanism of action
h-1 receptor antagonist; blocks action of histamine; possesses sedative, anti-motion, antiemetic and anticholinergic activity, potentiates the effects of narcotics to induce analgesia
Phenergan (promethazine) indications
nausea, vomitting, motionsickness sedation for patients in labor, potentation of analegics effects of narcotics
Phenergan (promethazine) contraindications
hypersensitivity, coma, cns-depressed pts from alcohol, barbituates, narcotics, reye's syndrome
Phenergan (promethazine) Adverse Reactions
Sedations, dizziness, impairment of mental and physical ability, arrhythmias, nausea, vomiting, hyperexcitability, halucinations, convulsions, and suddend death when used in children
Phenergan (promethazine) Drug interactions
Additive with other CNS depressants. Increased extrapyramidal effects with MAOIs
Phenergan (promethazine) Dose and admin
12.5 - 25mg IV Deep IM, PO rectally
Phenergan (promethazine) duration of ations
onset IV: Immediate. Peak effect: 30-60min duration 4-6 hours
Diazepam (valium) class
Benzodiazepine, sedative-hypnotic, anticovulsant
Diazepam (valium) Mechanism of action
potentiates effects of inhibatory neurotransmitters. Raises seizure threshold. induces amnesia and sedation
Diazepam (valium) indications
acute anxiety states. acute alcohol witdrawal, muscle relaxant, seizure activity, agitiation, analgesia for medical proceedures,
Diazepam (valium) contraindications
hypersensitivity, glaucoma, coma, shock, substance abuse, head injury
Diazepam (valium) adverse reactions
respiratory depression, hypotension, drowsiness, ataxia, reflex tachycardia, nausea, confussion, trombosis and phebitis
Diazepam (valium) drug interactions
incompatible with most drugs and fluids
Diazepam (valium) doseage and admin
seizure: adult 5-10mg IV q 10-15 min prm. (5mg every 5min) Max 30mg
Diazepam (valium) Duration of action
onset: 1-5min peak: minutes duration: 20 - 50min