Drug Guide

Generic Name

Hydrocodone Bitartrate with Guaifenesin

Brand Names Flowtuss, Obredon, Xtrelus

Classification

Therapeutic: Cough Suppressant and Expectorant

Pharmacological: Opioid analgesic and expectorant combination

FDA Approved Indications

  • Cough suppression associated with cold, bronchitis, or other respiratory conditions

Mechanism of Action

Hydrocodone binds to opioid receptors in the central nervous system to suppress cough reflex; Guaifenesin increases mucus expulsion by thinning airway secretions.

Dosage and Administration

Adult: Typically 10 mL every 4-6 hours as needed, not exceeding 60 mL per day.

Pediatric: Careful dosing based on age and weight, generally not recommended under age 6.

Geriatric: Dose adjustments may be necessary due to increased sensitivity and potential for respiratory depression.

Renal Impairment: Use with caution; consider dose adjustments.

Hepatic Impairment: Use with caution; monitor closely, as metabolism may be impaired.

Pharmacokinetics

Absorption: Rapid gastric absorption.

Distribution: Widely distributed; crosses blood-brain barrier.

Metabolism: Metabolized in liver, primarily via phase I and phase II reactions.

Excretion: Renal elimination of metabolites.

Half Life: Hydrocodone: approximately 3.5 hours; Guaifenesin: about 1 hour.

Contraindications

  • Hypersensitivity to hydrocodone or guaifenesin.
  • Use in cases of respiratory depression, severe asthma, or gastrointestinal obstruction.

Precautions

  • Use with caution in elderly, patients with head injury, respiratory depression, or hepatic impairment.
  • Potential for dependence and abuse.

Adverse Reactions - Common

  • Drowsiness (Common)
  • Dizziness (Common)
  • Nausea (Common)
  • Constipation (Common)

Adverse Reactions - Serious

  • Respiratory depression (Rare)
  • Allergic reactions, including rash or swelling (Rare)
  • Seizures (Rare)

Drug-Drug Interactions

  • Other central nervous system depressants, including alcohol, benzodiazepines, and sedatives.
  • MAO inhibitors – risk of serotonin syndrome or respiratory depression.

Drug-Food Interactions

  • Alcohol may increase sedative effects.

Drug-Herb Interactions

  • Use caution with herbs that cause sedation, such as kava or valerian.

Nursing Implications

Assessment: Assess for respiratory status, level of sedation, and bowel function.

Diagnoses:

  • Risk for respiratory depression.
  • Impaired gas exchange.

Implementation: Administer with food if gastrointestinal upset occurs. Monitor respiratory rate and sedation level.

Evaluation: Monitor effectiveness in suppressing cough and reducing mucus viscosity.

Patient/Family Teaching

  • Advise against activities requiring alertness until response to medication is known.
  • Warn about potential drowsiness and dizziness.
  • Ensure adequate hydration to loosen mucus.

Special Considerations

Black Box Warnings:

  • Potential for addiction, abuse, and misuse, leading to serious side effects including death.
  • Respiratory depression risks, especially in children and opioid-naïve individuals.

Genetic Factors: Genetic variations in CYP2D6 enzyme may affect metabolism and response.

Lab Test Interference: May interfere with certain assessments of respiratory function.

Overdose Management

Signs/Symptoms: Respiratory depression, somnolence, pinpoint pupils, hypotension, coma.

Treatment: Airway management, naloxone administration for respiratory depression, supportive measures.

Storage and Handling

Storage: Store at controlled room temperature, 20-25°C (68-77°F).

Stability: Stable when stored properly; check expiration dates.

This guide is for educational purposes only and is not intended for clinical use.