What is the recommended dosage of intramuscular (IM) Phenergan (promethazine)?

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IM Phenergan (Promethazine) Dosage

The recommended IM dose of promethazine for adults is 25 mg, which may be repeated within 2 hours if necessary for allergic conditions, or 12.5-25 mg every 4 hours for nausea/vomiting, with deep intramuscular injection being the preferred and safest parenteral route. 1

Adult Dosing by Indication

Allergic Conditions

  • Standard dose: 25 mg IM 1
  • May repeat within 2 hours if necessary 1
  • Transition to oral route as soon as circumstances permit 1
  • For allergic reactions to blood or plasma: 25 mg IM 1

Nausea and Vomiting

  • Dose: 12.5-25 mg IM 1
  • Do not repeat more frequently than every 4 hours 1
  • When used postoperatively, reduce concomitant analgesic and barbiturate doses accordingly 1

Sedation (Hospitalized Patients)

  • Nighttime sedation: 25-50 mg IM 1

Preoperative/Postoperative Use

  • Dose: 25-50 mg IM 1
  • Combine with appropriately reduced doses of analgesics and atropine-like drugs 1
  • Reduce concomitant analgesic or hypnotic medication accordingly 1

Obstetric Use

  • Early labor sedation: 50 mg IM 1
  • Established labor: 25-75 mg IM (average 50 mg) with reduced narcotic dose 1
  • May repeat once or twice at 4-hour intervals if necessary 1
  • Maximum total dose: 100 mg in 24 hours during labor 1

Pediatric Dosing

Critical Age Restrictions

  • Contraindicated in children under 2 years of age 1
  • For children ≥2 years: use lowest effective dose and avoid concomitant respiratory depressants 1

Administration Technique and Safety

Route Selection Priority

  • Deep intramuscular injection is the preferred parenteral route 1
  • Subcutaneous injection is contraindicated due to tissue necrosis risk 1
  • Under no circumstances give intra-arterially due to severe arteriospasm and gangrene risk 1

IV Administration (When Necessary)

  • Maximum concentration: 25 mg/mL 1
  • Maximum rate: 25 mg per minute 1
  • Preferably inject through functioning IV infusion set tubing 1
  • Stop immediately if patient complains of pain to evaluate for arterial injection or extravasation 1

Critical Safety Considerations

Tissue Injury Risk

  • Promethazine can cause severe chemical irritation and tissue damage regardless of route 1
  • Risks include perivascular extravasation, unintentional intra-arterial injection, and intraneuronal/perineuronal infiltration 1

Cardiovascular Effects

  • Research demonstrates minimal effect on autonomic cardiovascular mechanisms at 50 mg IM dose 2
  • No significant changes in resting heart rate, blood pressure, baroreflex function, or plasma catecholamines at 3 or 19.5 hours post-injection 2

Sedation and Performance Impact

  • 25 mg IM promethazine without amphetamine produces performance decrements equivalent to blood alcohol level of 25-50 mg% (1-2 drinks) 3
  • Drowsiness reported at 6 hours post-IM injection in 60% of subjects due to slow absorption 3
  • Most subjects report drowsiness, with some experiencing nervous excitation, dry mouth, and fatigue 2

Drug Interactions

  • Increased respiratory depression risk when combined with opioids or other CNS depressants 1
  • Reduce analgesic and sedative doses when used concomitantly 1

Common Pitfalls to Avoid

  • Never use IV route as first-line—IM is preferred and safer 1
  • Never give subcutaneously—causes tissue necrosis 1
  • Never exceed 4-hour dosing intervals for nausea/vomiting 1
  • Do not use in vomiting of unknown etiology in children and adolescents 1
  • Inspect solution before use; do not use if discolored or contains precipitate 1

References

Research

Promethazine affects autonomic cardiovascular mechanisms minimally.

The Journal of pharmacology and experimental therapeutics, 1997

Research

Side effects of antimotion sickness drugs.

Aviation, space, and environmental medicine, 1984

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.

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