Hydrocodone Bitartrate/Pseudoephedrine Hydrochloride
Pronouncation: (HIGH-droe-KOE-dohn by-TAR-trate/SUE-doe-eh-FED-rin HIGH-droe-KLOR-ide)
Class: Antitussive combination
Trade Names:
Detussin
- Liquid 5 mg hydrocodone bitartrate and 60 mg pseudoephedrine hydrochloride
Trade Names:
P-V-Tussin
- Tablets 5 mg hydrocodone bitartrate and 60 mg pseudoephedrine hydrochloride
Mechanism of Action
Pharmacology
Hydrocodone
Suppresses cough reflex; stimulates opiate receptors in the CNS and peripherally blocks pain impulse generation.
Pseudoephedrine
Causes vasoconstriction and subsequent shrinkage of nasal mucous membranes by alpha-adrenergic stimulation, which promotes nasal drainage.
Indications and Usage
Suppression of cough and relief of nasal congestion and other symptoms associated with the common cold, allergies, hay fever, sinusitis, and other respiratory illnesses.
Contraindications
Hypersensitivity to any component of product, or hypersensitivity or idiosyncrasy to sympathomimetic amines which may be manifested by insomnia, dizziness, weakness, tremor, or arrhythmias. Patients known to be hypersensitive to other sympathomimetic amines may exhibit cross sensitivity with pseudoephedrine. Sympathomimetic amines are contraindicated in patients with severe hypertension, severe coronary artery disease, and patients on MAOI therapy. P-V-Tussin tablets are contraindicated in breast-feeding mothers because of the higher than usual risk for infants from sympathomimetic amines.
Dosage and Administration
Liquid
Adults
PO 1 tsp (5 mL) 4 times daily.
Tablets
Adults
PO 1 tablet every 4 to 6 h (max, 4 in 24 h).
General Advice
Measure and administer prescribed dose of liquid using dosing syringe, dosing spoon, or dosing cup.
Storage/Stability
Store elixir at controlled room temperature (59° to 86°F). Keep tightly capped.
Drug Interactions
Alcohol, CNS depressants, narcotic analgesics, phenothiazines or other tranquilizers, sedative-hypnotics
Increased CNS depression (eg, drowsiness) may occur.
Laboratory Test Interactions
None well documented.
Adverse Reactions
Cardiovascular
Hydrocodone
Hypotension; bradycardia.
Pseudoephedrine
Cardiac arrhythmia; increased heart rate; increased BP.
CNS
Hydrocodone
Lightheadedness; dizziness; sedation; drowsiness; weakness; anxiety; fear; fatigue; dysphoria; psychological dependence; confusion.
Pseudoephedrine
Convulsions; CNS stimulation; hallucinations; tremors.
GI
Hydrocodone
Nausea; vomiting; constipation.
Genitourinary
Hydrocodone
Decreased urination; urethral spasm.
Pseudoephedrine
Dysuria.
Respiratory
Hydrocodone
Dyspnea; respiratory depression; irregular breathing.
Pseudoephedrine
Respiratory difficulties.
Miscellaneous
Pseudoephedrine
Pallor.
Precautions
Pregnancy
Consult health care provider before use.
Lactation
Consult health care provider before use.
Hydrocodone
Excreted in breast milk.
Special Risk Patients
As with any narcotic, P-V-Tussin tablets should be given with caution to certain patients such as the elderly or debilitated and those with severe impairment of hepatic or renal function, hypothyroidism, Addison disease, prostatic hypertrophy or urethral stricture, asthma, and narrow angle glaucoma.
Dependence
Hydrocodone has abuse potential; may be habit forming.
Overdosage
Symptoms
Hydrocodone
Respiratory and CNS depression, circulatory collapse, cardiopulmonary arrest, death
Pseudoephedrine
Cardiac arrhythmias, cerebral hemorrhage, pulmonary edema, palpitations, tremor, dizziness, vomiting, fear, labored breathing, headache, dryness of mouth, pallor, weakness, panic, anxiety, confusion, hallucination, delirium
Patient Information
- Advise patient to take prescribed dose up to 4 times daily as needed.
- Advise caregiver to use dosing spoon or syringe when giving elixir to children.
- Advise patient to take with food or milk if GI upset occurs.
- Advise patient to take last dose late in the afternoon or early evening to reduce chance of drug causing sleeplessness.
- Advise patient that if a dose is missed to take as soon as remembered unless it is nearing time for the next dose. Caution patient not to double the dose to catch up.
- Advise patient that if symptoms are not controlled, not to increase the dose of medication but to inform health care provider.
- Caution patient that drug may cause drowsiness and to use caution while driving or performing other tasks requiring mental alertness until tolerance is determined.
- Advise patient to avoid alcohol and other CNS depressants because of risk of excessive sedation.
- Caution patient not to take any OTC decongestants while taking this medication unless advised by health care provider.
- Instruct patient to stop taking drug and immediately report any of the following symptoms to health care provider: nervousness, dizziness, sleeplessness.
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