Atarax

Atarax

Generic Name

Atarax

Mechanism

  • Histamine H₁‑receptor antagonism: blocks peripheral postsynaptic H₁ receptors, leading to reduced pruritus, vasodilatation, and uterine relaxation.
  • Central nervous system (CNS) sedation: hydroxyzine crosses the blood‑brain barrier and exerts central H₁ blockade, producing anxiolytic and hypnotic effects.
  • Anticholinergic activity: modest inhibition of muscarinic receptors → dry mouth, blurred vision, constipation.
  • Neutralization of mast‑cell mediator release: reduces histamine and polypeptide release, beneficial in allergic inflammation.

Pharmacokinetics

  • Absorption: oral bioavailability ~85 % (rapid, peak plasma concentration within 1–3 h).
  • Distribution: extensive tissue distribution, high protein binding (~86 % to albumin).
  • Metabolism: hepatic N‑demethylation → primarily inactive metabolites; minimal CYP involvement.
  • Elimination: renal excretion (~80 % as metabolites); mean elimination half‑life 20–25 h (single dose). Renal impairment prolongs half‑life.
  • Special Populations:
  • Geriatric: increased sensitivity; consider starting lower dose.
  • Hepatic/Cirrhosis: no dosage adjustment needed (low hepatic metabolism).
  • Renal: reduce dose or defer dosing if CrCl <30 mL/min.

Indications

  • Anxiety (short‑term adjunctive treatment).
  • Premedication for sedation in minor procedures or to manage agitation.
  • Allergic conditions: urticaria, pruritus, and allergic rhinitis.
  • Nausea & vomiting (antiemetic).
  • Adjunctive therapy in management of atopic dermatitis when topical agents insufficient.

Contraindications

  • Contraindications:
  • Known hypersensitivity to hydroxyzine or phenothiazine derivatives.
  • Severe hepatic disease (rare).
  • Ocular hypertension or narrow‑angle glaucoma (risk of intra‑ocular pressure rise).
  • Warnings:
  • Central anticholinergic toxicity in high doses or with CNS‑acting drugs.
  • QT prolongation: avoid in patients with pre‑existing QT disorders or when co‑prescribed with drugs that prolong QT.
  • Sedation: risk of falls in elderly; advise against driving or operating machinery.
  • Pregnancy: category B; use with caution, only if benefit outweighs risk.
  • Breastfeeding: excreted in milk—consider alternative when possible.

Dosing

  • Adults: 25 mg orally every 4–6 h as needed (max 200 mg/day).
  • Children (≥12 yrs): 10–25 mg orally every 4–6 h (max 100 mg/day).
  • Pregnancy: 25 mg PO 2–3×/day adequate for anxiety; no evidence of teratogenicity.
  • Renal impairment (CrCl 30–50 mL/min): 25 mg every 8 h.
  • Elderly: start with 10 mg PO once; titrate as needed.
  • Intravenous (rarely used): 50 mg IV over 5 min, repeat as needed; monitor for hypotension.

Adverse Effects

  • Common
  • Somnolence, dizziness, mental dullness.
  • Dry mouth, blurred vision, urinary retention.
  • Headache, mild ataxia.
  • Serious
  • Anticholinergic crisis (severe CNS depression, hyperthermia, seizures).
  • Paradoxical agitation or anxiety in some patients.
  • QT‑interval prolongation → torsades de pointes (rare).
  • Severe allergic reactions (anaphylaxis) with rare immediate hypersensitivity.

Monitoring

  • Vital signs: pulse, BP, and respiration noted before dosing in high‑risk scenarios.
  • Neurologic: monitor consciousness, especially in elderly or those receiving CNS agents.
  • Cardiac: assess baseline ECG in patients with known QT prolongation; repeat if symptomatic.
  • Renal: creatinine clearance assessment in renal‑impaired patients for dose titration.
  • Patient counselling: on potential for sedation, handling of muscarinic side‑effects, and avoidance of alcohol or CNS depressants.

Clinical Pearls

  • Drug Interactions: synergistic CNS depression when combined with opioids, benzodiazepines, or alcohol. Avoid or titrate proactively.
  • Cardiovascular use: hydroxyzine can mask palpitations; monitor carefully in patients with arrhythmias.
  • Pre‑operative adjunct: can reduce pre‑operative anxiety and facilitate intubation; dose 25 mg 30 min pre‑op.
  • Dry Mouth & Dental Health: prescribe over‑the‑counter saliva substitutes or anticholinergic‑free hyaluronic acid gel to prevent xerostomia‑related complications.
  • Alternative indications: hydroxyzine’s anxiolytic effect is beneficial in sleep disorders; a single 50 mg dose may improve sleep quality in short-term use.
  • Contra‑Indication Detective: check for narrow‑angle glaucoma or ocular hypertension before commencing Atarax; consider screening with slit‑lamp exam if history unclear.
  • Drug‑Loading: a brief 12‑h loading of 50 mg per day is sometimes used for severe pruritus, but watch for cumulative sedation.

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Key pharmacology terms: *hydroxyzine*, *first‑generation antihistamine*, *H₁ antagonist*, *anticholinergic*, *QT prolongation*, *anxiety*, *pruritus*, *ulnar*, *renally cleared*.

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• For further updates and evidence‑based dosage recommendations, refer to the latest FDA prescribing information and peer‑reviewed pharmacology texts.

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

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