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Probenecid Concomitant administration of oral ketorolac tromethamine and probenecid resulted in decreased clearance and volume of distribution of ketorolac and significant increases in ketorolac plasma levels (total AUC increased approximately threefold from 5.4 to 17.8 mcg/h/mL) and terminal half-life increased approximately twofold from 6.6 to 15.1 hours

Prior authorization requirements can change at any time so its important that you should check your up-to-date UHC plan documents for the most recent description of benefits, limitations, exclusions and conditions of coverage

This represents a critical advantage over conventional antidepressants that typically require 2-6 weeks to produce therapeutic effects in humans