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How much hydrocodone is in hydrocodone homatropine solution?

4 min read

Typically, hydrocodone homatropine solution contains 5 milligrams (mg) of hydrocodone bitartrate for every 5 milliliters (mL) of solution, according to official prescribing information. This standard concentration is critical for understanding the correct dosage and ensuring the medication is used safely and effectively.

Quick Summary

Hydrocodone homatropine oral solutions usually contain 5mg of hydrocodone bitartrate per 5mL. This article details the standard concentration, the role of each component, general administration information, and essential safety precautions for this controlled substance.

Key Points

  • Standard Concentration: A typical hydrocodone homatropine solution contains 5mg of hydrocodone bitartrate per 5mL of liquid.

  • Abuse Deterrent: Homatropine is included in a subtherapeutic amount to discourage intentional overdose and potential abuse of the hydrocodone component.

  • Accurate Measurement is Vital: Always use a proper milliliter-calibrated measuring device to avoid accidental overdose, as household teaspoons are inaccurate.

  • Schedule II Controlled Substance: The medication has a high potential for addiction and abuse, making strict medical supervision and careful dispensing necessary.

  • Risk of Respiratory Depression: Use carries a significant risk of life-threatening respiratory depression, particularly with higher doses or concurrent use of other CNS depressants.

  • Adult-Only Prescription: The solution is typically reserved for adult patients aged 18 and older, and its use is not recommended for pediatric patients due to serious risks.

In This Article

Standard Concentration and Formulation

Hydrocodone homatropine oral solution, often sold under brand names such as Hycodan and generic versions, has a consistent and standardized concentration. This stability is vital for physicians and pharmacists to prescribe and dispense the correct dose and for patients to understand their medication.

  • Standard Concentration: The typical formulation contains 5 mg of hydrocodone bitartrate and 1.5 mg of homatropine methylbromide per 5 mL of oral solution.
  • Dosage per Milliliter: This means there is 1 mg of hydrocodone per milliliter of the solution (5 mg divided by 5 mL).
  • Measuring Accurately: Due to the potent nature of hydrocodone, it is crucial to use an accurate milliliter measuring device, such as an oral syringe or a marked medicine cup, provided by a pharmacist. A regular household teaspoon is not an accurate measuring tool and can lead to accidental overdosage.

The Role of Each Ingredient

Hydrocodone homatropine is a combination medication where each component serves a specific purpose.

Hydrocodone Bitartrate:

  • Function: An opioid antitussive (cough suppressant) that acts on the central nervous system to reduce the cough reflex.
  • Drug Classification: Classified as a Schedule II controlled substance due to its high potential for addiction, abuse, and misuse.
  • Primary Effect: Provides symptomatic relief from cough in adults.

Homatropine Methylbromide:

  • Function: An anticholinergic included in a subtherapeutic amount (an amount too small to be medically effective on its own).
  • Primary Effect: Acts as an abuse deterrent. The unpleasant side effects of homatropine are designed to discourage intentional overdosage of the hydrocodone component.

Administration

Hydrocodone homatropine oral solution is for adults 18 years of age and older. It is important to adhere strictly to the prescribed dose and frequency.

  • Measuring Accuracy: Always use a calibrated measuring device to ensure the correct dose is administered. Errors in measurement can lead to accidental overdose.
  • Duration of Use: This medication should be used for the shortest possible duration to achieve the treatment goal. An unresponsive cough after 5 days or sooner should be reevaluated by a healthcare provider to check for other underlying medical issues.

Potential Risks and Safety Precautions

Because hydrocodone is an opioid, its use carries significant risks that both patients and healthcare providers must be aware of. The FDA includes a boxed warning for these risks.

Life-Threatening Respiratory Depression

One of the most serious risks associated with hydrocodone is respiratory depression, which can be fatal. The risk is highest during the initiation of therapy and when increasing the dose. Patients with chronic pulmonary diseases, the elderly, or those who are debilitated are at an increased risk.

Risk of Addiction and Abuse

As a Schedule II controlled substance, hydrocodone carries a significant risk of addiction, abuse, and misuse. It is sought by individuals with substance use disorders, and physicians must assess a patient's risk before prescribing.

Medication Errors

Accidental overdose can occur due to medication errors. Clear communication from the prescriber and pharmacist is necessary, and patients should be instructed on how to use the provided measuring device correctly.

Drug-Drug Interactions

Concomitant use of hydrocodone with other central nervous system (CNS) depressants, such as alcohol, benzodiazepines, or other opioids, can result in profound sedation, respiratory depression, coma, and death. Patients should also avoid use with CYP3A4 inhibitors (like certain antibiotics) or inducers, as these can alter hydrocodone levels in the blood.

Comparison Table: Hydrocodone Homatropine Solutions vs. Tablets

While the oral solution is a common form, hydrocodone homatropine is also available in tablet form. Understanding the differences is important for patient safety.

Feature Oral Solution Tablets
Hydrocodone Content 5 mg per 5 mL 5 mg per tablet
Homatropine Content 1.5 mg per 5 mL 1.5 mg per tablet
Dosage Measurement Requires an accurate milliliter measuring device Taken as a whole tablet
Maximum Daily Use Should not exceed the amount specified by a healthcare professional Should not exceed the amount specified by a healthcare professional
Formulation Typically a flavored, red liquid Solid, scored tablets
Controlled Substance Class Schedule II Schedule II

Conclusion

Hydrocodone homatropine oral solution typically contains 5 mg of hydrocodone bitartrate per 5 mL of liquid. The other ingredient, homatropine, is present in a subtherapeutic dose to discourage abuse. This medication is a powerful, Schedule II opioid antitussive with significant risks, including addiction and potentially fatal respiratory depression. Safe and effective use depends on strict adherence to the prescribed dosage, accurate measurement using a proper device, and an awareness of potential drug interactions and side effects. For this reason, it is reserved for adult patients and prescribed for the shortest duration possible. Patients should consult with a healthcare professional to ensure they fully understand the risks and benefits of this medication.

For more information on drug safety, you can visit the official FDA website: https://www.fda.gov/drugs.

Frequently Asked Questions

The standard concentration is 5 milligrams (mg) of hydrocodone bitartrate per 5 milliliters (mL) of oral solution.

Homatropine is included in a subtherapeutic amount to discourage abuse of the hydrocodone. If a person takes an overdose, the homatropine can cause unpleasant side effects.

For adults, the administration should be as directed by a healthcare professional.

No, the use of hydrocodone homatropine solution is not recommended for pediatric patients, especially those younger than 6, due to the high risk of life-threatening respiratory depression.

You should use a calibrated milliliter measuring device provided by your pharmacist. Never use a household teaspoon, as its inaccurate size can lead to dosing errors and accidental overdose.

Yes, hydrocodone is classified as a Schedule II controlled substance due to its potential for addiction, abuse, and misuse.

Common side effects include sedation, dizziness, lightheadedness, nausea, vomiting, and constipation.

If your cough does not improve within 5 days, or even sooner, you should contact your healthcare provider. The administration should not be increased without medical advice, as this could be a sign of an underlying medical issue.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.