What is the dosage and usage of prochlorperazine for treating nausea and vomiting, and schizophrenia?

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Prochlorperazine Dosage and Usage for Nausea/Vomiting and Schizophrenia

For nausea and vomiting, prochlorperazine is typically administered at 5-10 mg orally every 6-8 hours as needed, while for schizophrenia, higher doses of 15-40 mg daily divided in multiple doses are recommended. 1

Nausea and Vomiting Treatment

Dosage Options:

  • Oral administration:
    • 5-10 mg every 6 hours as needed 2
    • 10 mg pretreatment (optional) for chemotherapy-induced nausea 2
  • Intravenous administration:
    • 5-10 mg every 6-8 hours 2
    • 2.5 mg slow IV push (can repeat after 20 minutes if needed) for rapid control 3
  • Rectal administration:
    • 25 mg suppository every 12 hours 2

Clinical Considerations:

  1. Efficacy: Prochlorperazine works significantly better than promethazine for relieving symptoms of nausea and vomiting more quickly and completely in emergency department patients 4

  2. Onset of action: Mean time to cessation of vomiting with IV administration is approximately 8.5 minutes versus 35 minutes for intramuscular administration 3

  3. Specific indications:

    • Low to moderate emetogenic potential chemotherapy 2
    • Postoperative nausea and vomiting 2
    • Opioid-induced nausea 5
    • Acute nausea in emergency settings 3, 4, 6
    • Cyclic vomiting syndrome 2
  4. Administration route options: Virtually all prochlorperazine formulations can be given intravenously at similar doses if the patient is unable to take oral medication 2

  5. Buccal formulation advantage: Buccal administration produces plasma concentrations more than twice as high as an oral tablet, with less than half the variability 7

Schizophrenia Treatment

Dosage:

  • FDA-approved for the treatment of schizophrenia 1
  • Higher doses than for antiemetic use are typically required
  • Dosing should be individualized based on response and tolerability

Important Adverse Effects and Precautions

Common adverse effects:

  • Extrapyramidal symptoms: Particularly akathisia, which can occur within a week of starting treatment 5
  • CNS depression 2
  • Anticholinergic effects 2

Monitoring and precautions:

  • Monitor for dystonic reactions: Use diphenhydramine 25-50 mg PO or IV every 4-6 hours for dystonic reactions 2
  • Caution in specific populations: Patients with history of leukopenia, neutropenia, dementia, glaucoma, or seizure disorder 2
  • Duration limitations: When used for non-psychotic anxiety, should not be administered at doses of more than 20 mg per day or for longer than 12 weeks due to risk of persistent tardive dyskinesia 1

Risk of extrapyramidal symptoms:

The incidence of extrapyramidal symptoms with prochlorperazine (14%) is significantly higher than with newer atypical antipsychotics like perospirone (0%) when used as antiemetics 5. Careful monitoring is essential, particularly for akathisia.

Alternative Antiemetics to Consider

When prochlorperazine causes side effects or is ineffective:

  • 5-HT3 antagonists (ondansetron, granisetron)
  • NK-1 receptor antagonists (aprepitant)
  • Other phenothiazines (promethazine, chlorpromazine)
  • Atypical antipsychotics with lower extrapyramidal side effect profiles 5

Administration in Special Circumstances

  • Peripheral IV administration: Can cause tissue injury, including gangrene or thrombophlebitis 2
  • Buccal administration: May provide higher and more consistent plasma levels with reduced metabolite formation 7

Always consider the risk-benefit profile when prescribing prochlorperazine, particularly for extended periods, due to the risk of tardive dyskinesia and other extrapyramidal symptoms.

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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