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hydrocodone/phenylpropanolamine (Hycomine, Codamine)

Indication: symptomatic relief of cough & nasal congestion Contraindications: 1) concurrent administration of MAO inhibitor 2) hypertension 3) hyperthyroidism 4) increased intracranial pressure 2) depressed ventilation Dosage: 1) adults & children > 12 years of age: a) 5-10 mL (5-10 mg hydrocodone) every 4-6 hours PRN b) maximum: 6 doses/24 hours 2) children 6-12 years of age: a) 2.5 mL (2.5 mg hydrocodone) every 4-6 hours PRN b) maximum: 6 doses/24 hours Syrup: hydrocodone bitartrate 5 mg & phenylpropanolamine HCl 25 mg/5 mL (120 mL) Adverse effects: 1) common (> 10%) - lightheadedness, dizziness, sedation, drowsiness, weakness, tiredness, hypotension 2) less common (1-10%) - shortness of breath, troubled breathing, confusion, diminished urination, nausea/vomiting, bradycardia, tachycardia 3) uncommon (< 1%) - hallucinations, hypertension, double vision, dry mouth, anorexia, miosis, biliary or urinary spasm, histamine release, hot & dry skin, impaired GI motility, mydriasis, blurred vision 4) other - rash - blood dyscrasias - nephrotoxicity with chronic use - hepatotoxicity - respiratory depression is dose & tolerance-related - tolerance & dependence - constipation Drug interactions: 1) naloxone is a direct opiate antagonist 2) CNS depressants 3) phenothiazines 4) tricyclic antidepressants (TCA)

Interactions

drug adverse effects of antitussive agent(s)

General

pharmacologic combination antitussive agent

References

Kaiser Permanente Northern California Regional Drug Formulary, 1998

Components

hydrocodone; dihydrocodeinone (Zohydro ER, Hysingla ER) phenylpropanolamine (PPA)