What over‑the‑counter medication (e.g., Dimetapp DM) contains brompheniramine combined with sustained‑release pseudoephedrine, and what is the recommended adult dosing schedule for a patient without contraindications?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 27, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Over-the-Counter Brompheniramine + Sustained-Release Pseudoephedrine Products

For adults without contraindications, the recommended regimen is brompheniramine 12 mg combined with sustained-release pseudoephedrine 120 mg taken twice daily (every 12 hours). 1

Available Formulations

  • Brompheniramine 12 mg + sustained-release pseudoephedrine 120 mg is the evidence-based combination specifically studied and recommended by the American College of Chest Physicians for upper airway cough syndrome and allergic rhinitis. 1

  • This combination is available as a sustained-release tablet formulation designed for twice-daily dosing (morning and evening, approximately 12 hours apart). 1, 2

  • Common brand names include various generic formulations; the specific product "Dimetapp DM" mentioned in your question typically contains dextromethorphan (a cough suppressant) rather than the pure brompheniramine-pseudoephedrine combination, so verify the exact formulation on the label. 3

Adult Dosing Schedule

  • Standard adult dose: One tablet (brompheniramine 12 mg + pseudoephedrine 120 mg sustained-release) every 12 hours. 1

  • Maximum duration: Limit use to the shortest necessary period, typically 3–7 days for acute symptoms; chronic use beyond 2 weeks without medical supervision is not recommended. 1, 4

  • Initiation strategy to minimize sedation: Start with once-daily dosing at bedtime for 2–3 days, then advance to twice-daily dosing if tolerated. 1

Absolute Contraindications

Before recommending this combination, screen for the following conditions that prohibit use:

  • Severe or uncontrolled hypertension – pseudoephedrine raises systolic blood pressure by approximately 1 mmHg on average, but individual responses vary widely and can trigger dangerous hypertensive spikes. 5

  • Symptomatic benign prostatic hypertrophy or urinary retention – the anticholinergic properties of brompheniramine worsen these conditions. 1

  • Narrow-angle glaucoma – anticholinergic effects increase intraocular pressure. 1, 4

  • Congestive heart failure or severe coronary artery disease – pseudoephedrine's vasoconstrictive effects can precipitate cardiac decompensation. 5

  • Concurrent monoamine oxidase inhibitor (MAOI) therapy – this combination can trigger hypertensive crisis. 5

  • Children younger than 6 years – serious adverse events including 69 antihistamine-related deaths (41 in children under 2 years) and 54 decongestant-related deaths were documented between 1969 and 2006; the FDA advises against use in this age group. 4

Relative Contraindications Requiring Monitoring

  • Controlled hypertension: May use with caution if blood pressure is monitored within 24–48 hours of initiation; discontinue immediately if systolic BP rises >20 mmHg or new symptoms develop. 5

  • Concurrent stimulant medications (e.g., methylphenidate for ADHD): The combination creates additive cardiovascular burden; if unavoidable, monitor BP and heart rate closely and limit decongestant use to 3–5 days maximum. 4

  • Hyperthyroidism, arrhythmias, or cerebrovascular disease: Use only if safer alternatives (intranasal corticosteroids, saline irrigation) are ineffective. 5, 4

Common Pitfalls to Avoid

  • Do not substitute second-generation antihistamines (cetirizine, loratadine, fexofenadine) for brompheniramine in this indication; they lack the anticholinergic properties necessary to reduce secretions and suppress cough in upper airway cough syndrome. 1

  • Do not combine with other sympathomimetic agents (caffeine, energy drinks, additional decongestants, or stimulants) because this substantially increases the risk of hypertensive crisis. 5, 4

  • Do not use for viral upper respiratory infections in otherwise healthy adults—European and American guidelines explicitly advise against antihistamines for post-viral rhinosinusitis because viral infections are not histamine-mediated; safer alternatives include analgesics, high-volume saline irrigation (≥150 mL), and intranasal corticosteroids. 1

  • Avoid NSAIDs (ibuprofen, naproxen) in combination products if the patient has hypertension, as NSAIDs can raise BP by an additional 3 mmHg systolic and blunt antihypertensive medications. 5

Safer Alternatives When Contraindications Exist

  • Intranasal corticosteroids (e.g., fluticasone 100–200 µg daily) have no cardiovascular effects and are the preferred first-line option for patients with hypertension or cardiac disease. 1, 5

  • High-volume nasal saline irrigation (≥150 mL) provides mechanical clearance with no systemic absorption. 1, 5

  • Second-generation antihistamines alone (loratadine, cetirizine, fexofenadine) are safe in hypertensive patients but are ineffective for upper airway cough syndrome; reserve them for allergic rhinitis without cough. 1, 5

Expected Clinical Response

  • Symptom improvement typically occurs within a few days to 2 weeks of starting therapy. 1

  • If no improvement after 2 weeks of adequate therapy, obtain sinus imaging (CT or radiographs) to evaluate for chronic sinusitis, and consider alternative diagnoses such as asthma, non-asthmatic eosinophilic bronchitis, or gastroesophageal reflux disease. 1

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.