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Hydrocodone is a highly selective full agonist of the μ-opioid receptor (MOR). [19] [45] [40] This is the main biological target of the endogenous opioid neuropeptide β-endorphin. [46] Hydrocodone has low affinity for the δ-opioid receptor (DOR) and the κ-opioid receptor (KOR), where it is an agonist similarly. [40]
In June 2009, a US Food and Drug Administration (FDA) advisory panel voted by a narrow margin to advise the FDA to remove Vicodin and another opioid, Percocet, from the market because of "a high likelihood of overdose from prescription narcotics and acetaminophen products". [21]
The two active components of the drug, ibuprofen and hydrocodone, do not affect each other's absorption characteristics or other pharmacokinetic parameters. [1] After an oral dose, the peak level of hydrocodone in the blood is reached 1.7 hours after administration. [1] The blood levels of ibuprofen peak 1.8 hours after oral administration. [1]
This page was last edited on 23 December 2023, at 08:42 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
This page was last edited on 21 December 2023, at 22:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
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Hydrocodone/aspirin is an oral combination drug formulation of the opioid analgesic hydrocodone and the nonsteroidal anti-inflammatory drug (NSAID) aspirin that is used in the treatment of chronic and acute pain.