Hycodan Oral Solution Dosage
Generic name: hydrocodone bitartrate 5mg, homatropine methylbromide 1.5mg
Dosage form: oral solution
Drug class: Upper respiratory combinations
Medically reviewed by Drugs.com. Last updated on Dec 19, 2024.
Important Dosage and Administration Instructions
Administer HYCODAN by the oral route only.
Always use an accurate milliliter measuring device when administering HYCODAN oral solution to ensure that the dose is measured and administered accurately. A household teaspoon is not an accurate measuring device and could lead to overdosage. For prescriptions where a measuring device is not provided, a pharmacist can provide an appropriate measuring device and can provide instructions for measuring the correct dose. Do not overfill. Rinse the measuring device with water after each use.
Advise patients not to increase the dose or dosing frequency of HYCODAN because serious adverse events such as respiratory depression may occur with overdosage. The dosage of HYCODAN should not be increased if cough fails to respond; an unresponsive cough should be reevaluated for possible underlying pathology.
Monitoring, Maintenance, and Discontinuation of Therapy
- Prescribe HYCODAN for the shortest duration that is consistent with individual patient treatment goals.
- Monitor patients closely for respiratory depression, especially within the first 24 to 72 hours of initiating therapy.
- Reevaluate patients with unresponsive cough in 5 days or sooner for possible underlying pathology, such as foreign body or lower respiratory tract disease. If a patient requires a refill, reevaluate the cause of the cough and assess the need for continued treatment with HYCODAN, the relative incidence of adverse reactions, and the development of addiction, abuse, or misuse.
- Do not abruptly discontinue HYCODAN in a physically-dependent patient. When a patient who has been taking HYCODAN regularly and may be physically dependent no longer requires therapy with HYCODAN, taper the dose gradually, by 25% to 50% every 2 to 4 days, while monitoring carefully for signs and symptoms of withdrawal. If the patient develops these signs or symptoms, raise the dose to the previous level and taper more slowly, either by increasing the interval between decreases, decreasing the amount of change in dose, or both.
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