Chlorpheniramine

Chlorpheniramine

Generic Name

Chlorpheniramine

Mechanism

  • H₁ receptor antagonism: Competitively blocks peripheral and central H₁ receptors, reducing vasodilation, capillary permeability, and smooth‑muscle contraction.
  • Anticholinergic effect: Inhibits muscarinic (M₁–M₄) receptors, contributing to sedation, xerostomia, and anticholinergic toxicity in high doses.
  • Limited blood‑brain barrier penetration leads to significant CNS side effects relative to newer antihistamines.

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Pharmacokinetics

ParameterTypical values
AbsorptionRapid; peak plasma concentration 0.5–1 h after oral dosing
Bioavailability~70 % (oral)
DistributionHighly protein‑bound (~99 %); crosses BBB
MetabolismHepatic via CYP2D6; oxidative deamination and glucuronidation
EliminationRenal (≈70 % unmetabolised), hepatic excretion of metabolites
Half‑life5–10 h (may extend to 12‑15 h in hepatic/renal impairment)
Onset of action15–20 min (rapid relief of allergic symptoms)

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Indications

  • Acute allergic rhinitis (hay fever)
  • Urticaria (hives)
  • Seasonal allergic conjunctivitis
  • Non‑infectious rhinitis/eczema-associated itching
  • First‑line adjunct in post‑operative sedation or nausea (when anticholinergic benefit desired)

*(Note: In many countries, over‑the‑counter formulations are limited to single‑dose use for acute symptoms.)*

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Contraindications

  • Absolute contraindications: Severe cardiovascular disease (e.g., uncontrolled arrhythmias, ischemic heart disease), narrow‑angle glaucoma, prostatic hypertrophy with urinary retention, pregnancy (Category C).
  • Precautions:
  • Elderly: increased sensitivity to sedation & anticholinergic effects.
  • Children <6 yrs: contraindicated; use caution in 6‑12 yrs for CNS effects.
  • Patients with liver or kidney impairment → dose adjustment.
  • Drug interactions:
  • MAO inhibitors, tricyclic antidepressants, sedatives, alcohol → additive CNS depression.
  • CYP2D6 inhibitors (e.g., fluoxetine) → elevated plasma levels.

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Dosing

Age/WeightAdultPediatric (6‑12 yrs)Infant (≤6 yrs)
Oral4 mg every 4‑6 h (max 24 mg/day)0.25 mg/kg/dose every 8 h (max 12 mg/day)Contraindicated
Intramuscular / Subcutaneous4–10 mg IM/SC (single dose)Not recommended
Nebulised2 mg/mL for respiratory allergies0.5 mg/kg/dose (max 3 mg)

*Adjust dose downward in hepatic/renal dysfunction.*

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Adverse Effects

Common
• Drowsiness & sedation
• Dry mouth, blurred vision
• Headache, dizziness
• Light‑headedness, orthostatic hypotension

Serious
• Anticholinergic toxicity (confusion, urinary retention, tachycardia)
• Severe hypersensitivity (rash, angioedema)
• Cardiac arrhythmias (rare, especially in patients with pre‑existing arrhythmias)
• CNS depression (when combined with other CNS depressants)

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Monitoring

  • Vital signs: BP, pulse, ECG in patients with cardiac disease
  • CNS status: level of alertness, sedation score (e.g., Ramsay)
  • Respiratory: especially if used IV/IM in patients with airway obstruction
  • Urinary function: in patients with prostatic hypertrophy
  • Laboratory: liver & renal panels if chronic use or dose adjustment needed

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Clinical Pearls

1. Anticholinergic profile matters – Use caution in elderly or patients with glaucoma; consider switching to a second‑generation antihistamine (cetirizine, loratadine) when anticholinergic side‑effects are problematic.

2. Sedation is a therapeutic advantage – In postoperative patients or those with severe allergic reactions causing sleep‑deprived symptoms, chlorpheniramine’s sedating properties can aid in rest and comfort.

3. Drug‑drug synergy – Combine with decongestants (pseudoephedrine) only after ruling out cardiac risk; the anticholinergic effect of chlorpheniramine can mask tachycardia induced by sympathomimetic decongestants.

4. Pediatric dosing formula – 0.25 mg/kg/dose; never exceed total of 12 mg/day; double‑check weight calculations to avoid overdose.

5. Over‑the‑counter caution – OTC products may contain 4‑mg tablets; a single dose is safe for adults, but repeat dosing >24 h without physician review can increase risk of overdose.

6. Renal impairment → dose reduction – Reduce to 2 mg every 6 h or halve the total daily dose; monitor serum creatinine.

7. Use a symptom‑based approach – If itching or sneezing is the only symptom, a second‑generation antihistamine may be preferable to avoid sedation.

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• > Key Takeaway: *Chlorpheniramine* remains a useful, readily available first‑generation antihistamine for acute allergic symptoms, especially when sedative effect is desired. Its anticholinergic activity and CNS penetration, however, necessitate mindful dosing and monitoring, particularly in vulnerable populations.

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Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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