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Isolated from Opium (agonist)
Metabolized to morphine (elicit analgesia)
Used to replace morphine (not thought to be addictive)
1960 Schedule II controlled substance
“Drug activation occurs when the CYP2D6 gene produces a hepatic drug-metabolizing enzyme, CYP2D6”(Kelly 322).
North Africans, Ethiopians, Saudi Arabians > Caucasian> African-Americans > Chinese or Japanese >Hispanics
Information
Metabolic Pathway•70% C6G•7% N-demethylation•5% O-demethylationCYP2D6•4% unchanged
•Liver, brain, intestine
Cough Suppressant due to mu
Mild-Moderate Pain reliever
19th century pain relief & diabetes control
Every 4-6 hours
Medical Uses
Purple Drank (sizzurp, lean syrup)
Starting Dose 30-60mg, settle at 250mg
Euphoria, elation, “liking”, analgesia
Dextromethorphan
Recreational Uses
Itching, constipation, dizziness, sedation, flushing, nausea, vomiting, and hives
Respiratory CNS Seizures Cardiac Arrest Increases pain sensitivity (TLR4)
Side Effects
Endorphin production decreased
Tolerance Withdrawal
Opioid Poisoning Coma Pinpoint Pupils Respiratory
Depression
Toxicity/Deaths
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Kelly, Patricia, A. "Pharmacogenomics: Why Standard Codeine Doses Can Have Serious Toxicities Or No Therapeutic Effect." Oncology Nursing Forum 40.4 (2013): 322-324. CINAHL Complete. Web. 21 Nov. 2014.
Lam, Jessica, et al. "Codeine-Related Deaths: The Role Of Pharmacogenetics And Drug Interactions." Forensic Science International 239.(2014): 50-56. Academic Search Premier. Web. 21 Nov. 2014.
Schwartz, Jason J., PhD. "Codeine." Salem Press Encyclopedia Of Health (2012): Research Starters. Web. 20 Nov. 2014
Sources