promazine hydrochloride: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
promazine hydrochloride: clinical details
Prescribing considerations
- Use only as an adjunct to non-pharmacological management for the selected licensed indication.
- Assess cardiac disease, QT risk, electrolytes, seizure risk, hepatic and renal function, Parkinsonism, glaucoma, prostatic enlargement, respiratory disease and venous-thromboembolism risk.
- Older people are especially susceptible to sedation, hypotension and impaired temperature regulation.
- Avoid abrupt discontinuation after ongoing treatment because withdrawal and movement disorders can occur.
- Consider high variability in systemic exposure and review effectiveness and toxicity.
Contraindications and cautions
- Hypersensitivity to promazine, other phenothiazines or relevant excipients
- Coma or central nervous system depression
- Bone-marrow depression
- Phaeochromocytoma
- Moderate or severe hepatic impairment
- Long-QT syndrome
- Pregnancy unless compelling reasons exist
- Breastfeeding
Monitoring
- Clinical response, sedation, postural blood pressure and falls risk
- Movement disorders, including akathisia, dystonia and tardive dyskinesia
- ECG and electrolytes when cardiac or QT risk factors are present
- Blood count if unexplained infection, fever or sore throat occurs
- Liver function and signs of jaundice
- During prolonged use, blood, cardiac-conduction and ocular effects
- Weight, metabolic effects, prolactin-related effects and venous-thromboembolism risk as clinically appropriate
Clinical pharmacology
Promazine is an aliphatic phenothiazine dopamine inhibitor with central depressant, alpha-adrenergic blocking and weaker anticholinergic activity. Oral absorption is followed by substantial first-pass and hepatic metabolism, extensive protein binding and wide interpatient variability in plasma exposure.
Formulation and product differences
- The selected preparation is an oral syrup requiring accurate volume measurement.
- It contains glucose, sucrose, propylene glycol, parabens and a small amount of ethanol; these excipients may matter in diabetes, sugar intolerance, renal or hepatic impairment, allergy risk and dental care.
- Store in the original bottle protected from light and observe the stated in-use shelf life.
promazine hydrochloride preparations and strengths
Syrup
Route: Oral
Strengths: 25 mg/5 mL, 50 mg/5 mL
promazine hydrochloride interactions
Promazine has clinically important sedative, cardiovascular, neurological and anticholinergic interactions. Check prescribed, non-prescription and herbal products with a pharmacist or prescriber.
Alcohol, opioids, sleeping medicines, anaesthetics and other CNS depressants
Sedation, impaired alertness and respiratory or central nervous system depression may be increased.
QT-prolonging medicines, including some antiarrhythmics, antibiotics, antidepressants and antipsychotics
The combination can increase the risk of dangerous ventricular arrhythmias.
Antihypertensives
Blood-pressure-lowering effects may be enhanced, increasing dizziness, falls or fainting.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.