Term
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Definition
IV, Liquid, Tabs, Suppositories Low oral bioavailabiltiy 30-40%, primarily IV can do IM Primarily phase II metabolism: glucoronidation at C3 and C6 OH groups Half-Life = 4 hours |
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Term
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Definition
5x morphine potency IV, liquid, IR trabs, ER tabs, suppositories: mainly an IV drug Oral bioavailability 75% Primarily phase II: glucoronidation at c3 and c6 OH groups. Half life < 2 hours = short acting HIGH RISK OF RESPIRATORY DEPRESSION |
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Term
Oxycodone (Percocet, roxicet) |
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Definition
same potency as IV morphine, stronger than oral. NO IV FORMS Oral bioavailability: 60-70% Primarily Phase I metabolism Half life: 4 hours One of the most diverted and abused RX in US ER tabs only for chronic |
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Term
Hydrocodone (Vicodin, Lortab) |
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Definition
50% morphine potency NO IV or IM |
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Term
Codeine (Tylenol III, Cough/Cold AC liquids) |
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Definition
10% potency of morphine. NO IV OR IM Weak/Poor choice Poorly GI tolerated Must metabolize |
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Term
Tramadol (Ultram, Ryzolt) |
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Definition
20% or less potency of Morphine No IV form Parent compound acts like an SNRI Active metabolite throuch cyp3a4 About 1/3 of drug is renally eliminated unchanged Oral bioavailability >70% Half-life = 7-8 hours Serotonin and seizure risk |
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Term
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Definition
100x potency of morphine No oral doses; better than 90% availability in dermal patches Primarily phase 1: cyp3a4 to inactivate metabolites Half-life <60 minutes (very short acting) Big-guns, extremely active mu kappa delta agonist, use to get people out quickly Huge risk for respitory |
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