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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)