Drug Guide
Dextromethorphan Polistirex
Classification
Therapeutic: Antitussive (cough suppressant)
Pharmacological: NMDA receptor antagonist, sigma-1 receptor agonist
FDA Approved Indications
- Relief of cough caused by minor throat and bronchial irritation
Mechanism of Action
Dextromethorphan acts centrally on the medullary cough center to elevate the threshold for coughing. It also acts as an NMDA receptor antagonist and sigma-1 receptor agonist, reducing cough reflex sensitivity.
Dosage and Administration
Adult: 20 mg every 4 hours, not to exceed 120 mg in 24 hours
Pediatric: 6-12 years: 10 mg every 12 hours or 20 mg every 4 hours (not to exceed 120 mg/day); under 6 years: consult pediatrician
Geriatric: Same as adult, cautious use due to potential CNS effects
Renal Impairment: Use with caution; dosage adjustments may be necessary
Hepatic Impairment: Use with caution; dosage adjustments may be necessary
Pharmacokinetics
Absorption: Well absorbed orally and sustained over time with polistirex formulation
Distribution: Widely distributed; crosses blood-brain barrier
Metabolism: Primarily hepatic via CYP2D6 and other enzymes
Excretion: Renal (metabolites) and fecal
Half Life: Approximately 3-6 hours
Contraindications
- Use in children under 4 years due to risk of accidental overdose and severe adverse effects
Precautions
- Use with caution in patients with a history of psychiatric disorders, chronic cough, or those taking serotonergic drugs due to risk of serotonin syndrome
Adverse Reactions - Common
- Dizziness (Common)
- Nausea or vomiting (Common)
- Drowsiness (Common)
Adverse Reactions - Serious
- Serotonin syndrome (when combined with serotonergic drugs) (Rare)
- Allergic reactions including rash, pruritus (Rare)
Drug-Drug Interactions
- Serotonergic agents (SSRIs, SNRIs, MAOIs) — risk of serotonin syndrome
- Central nervous system depressants — increased sedation
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess for cough severity, medication adherence, and history of psychiatric or respiratory conditions
Diagnoses:
- Risk of injury due to dizziness or drowsiness
Implementation: Administer with food or milk to reduce GI upset, monitor response and adverse effects
Evaluation: Effective cough suppression without adverse effects
Patient/Family Teaching
- Do not exceed recommended dose.
- Avoid alcohol and CNS depressants.
- Report signs of allergic reactions or serotonin syndrome.
- Seek medical advice before use with other serotonergic drugs.
Special Considerations
Black Box Warnings:
- Risks of abuse and misuse due to psychoactive properties, especially in adolescents and young adults.
Genetic Factors: CYP2D6 metabolizer status may affect drug levels and response.
Lab Test Interference: No known significant interference.
Overdose Management
Signs/Symptoms: Dizziness, nausea, vomiting, hallucinations, serotonin syndrome symptoms (agitation, hyperthermia, muscle rigidity)
Treatment: Supportive care, activated charcoal if recent ingestion, benzodiazepines for agitation or seizures, evaluate for serotonin syndrome, and maintain airway.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F). Keep container tightly closed.
Stability: Stable for 2-3 years, check expiration date.