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Medic Drug Review 2

Across
MOA: Blocks (inhibits) acetylcholine at bronchial smooth muscle receptor sites; Contraindication: Hypersensitivity to Atropine
Contraindication: Hypotension; Indication: Sedation for excited delirium; Dose: 2-10 mg
MOA: Displaces opioids and binds to the opioid receptors in the Central Nervous System blocking the effects of both natural and synthetic narcotics
Dose: 0.25 mg/kg IVP over 2 min
Trade Name; Dose: 2.5 to 5 mg IV bolus over 2 - 3 min
Indication: Sedation agent to facilitate endotracheal intubation; MOA: Interrupts the pathways within the cortex of the limbic system
Indication: Moderate to severe pain – musculoskeletal injuries, etc.; MOA: 5 times more potent per mg than morphine
Indication: Acute exacerbation of Chronic Obstructive Pulmonary Disease (COPD); MOA: Anti-inflammatory effect in management of allergic reactions and anaphylactic shock
Contraindication: uncontrolled airway, absent gag reflex, or unable to swallow; Trade Name
Indication: laryngotracheobronchitis (Croup); Contraindication: Epiglottitis; Trade Name
Indication: Long-term muscle paralysis to facilitate endotracheal intubation; Dose: 0.1 mg/kg
Down
MOA: Depresses the reticular activating system (RAS) by stimulating the GABA receptors thereby inducing rapid unconsciousness; Dose: 0.3 mg/kg
Indication: Unstable angina
Dose: 25 grams in 50 mL IVP
Indication: Chest pain secondary to MI; Contraindication: Hypotension; Dose: 2-10 mg
Contraindication: Known hypersensitivity; Dose: 4-24 mg
MOA: Vasodilation of veins and arteries, particularly coronary arteries, by direct action on the smooth muscle of the vessel; Dose: 0.4 mg SL
Dose: 0.25 mg SC; Indication: Acute asthma attack
MOA: Slows conduction through AV node thereby terminating reentrant tachycardia; Contraindication: Second Degree Type II and Third Degree Heart Blocks
Dose: 2 to 5 mg; MOA: By blocking the cholinergic receptors at the neuroglandular junctions it blocks the overstimulation of the glands and therefore decreases salivation, lacrimation, urination, defecation, gastric motility, emesis
MOA: Works as competitive antagonist to ACh at post-synaptic receptors in the cholinergic receptor sites at the neuromuscular junction (NMJ); Dose: 1 mg/kg; Duration: 45-70 min