Is Compazine (prochlorperazine) nephrotoxic?

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Is Compazine (Prochlorperazine) Nephrotoxic?

Prochlorperazine (Compazine) is not considered nephrotoxic and does not appear on established lists of nephrotoxic medications in current clinical guidelines. Based on the available evidence, there is no indication that Compazine causes direct kidney injury or dysfunction.

Understanding Drug-Induced Nephrotoxicity

When evaluating a medication's potential for nephrotoxicity, it's important to understand how drugs can affect kidney function:

  • Drugs can cause kidney dysfunction through systemic or renal/glomerular hemodynamic effects, or cause structural damage through tubular or glomerular cell injury 1
  • Nephrotoxic medications typically work through mechanisms such as:
    • Direct tubular toxicity
    • Glomerular damage
    • Crystal formation and obstruction
    • Interstitial nephritis
    • Hemodynamic alterations 1

Prochlorperazine's Safety Profile

Prochlorperazine (Compazine) is a phenothiazine antiemetic and antipsychotic medication commonly used for:

  • Treatment of nausea and vomiting
  • Management of psychotic disorders
  • Adjunctive therapy in migraine headaches 1

The adverse effects profile of prochlorperazine includes:

  • Hypotension, tachycardia, arrhythmias
  • Extrapyramidal symptoms (akathisia, pseudo-parkinsonism, tardive dyskinesia, dystonia)
  • CNS effects (dizziness, sedation)
  • Anticholinergic effects (xerostomia, constipation, urinary retention, blurred vision)
  • Other effects (nasal congestion, decreased diaphoresis) 1

Notably absent from this list is nephrotoxicity or renal adverse effects.

Established Nephrotoxic Medications

For comparison, medications with well-documented nephrotoxicity include:

  • Aminoglycosides (amikacin, kanamycin) which can cause direct tubular damage 1
  • Amphotericin B, which affects up to 80% of treated patients with various renal effects 1
  • Cidofovir, foscarnet, and pentamidine, which have known nephrotoxic potential 1
  • Various antimicrobials that can cause acute interstitial nephritis, acute tubular necrosis, or crystal deposition 2, 3, 4

Clinical Implications and Recommendations

When prescribing medications to patients with kidney concerns:

  • Potentially nephrotoxic agents should be used only when needed and for as short a duration as possible 1
  • Kidney function should be monitored in patients exposed to known nephrotoxic agents 1
  • While many medications require dose adjustments in renal impairment, there is no specific recommendation for prochlorperazine dose adjustment in patients with kidney disease 5

Conclusion for Clinical Practice

When considering prochlorperazine for patients:

  • Prochlorperazine can be used without specific concerns about nephrotoxicity 1
  • Standard monitoring of renal function as part of routine care is appropriate, but specific monitoring for nephrotoxicity is not required 1
  • Focus monitoring on prochlorperazine's known adverse effects, particularly extrapyramidal symptoms and cardiovascular effects 1

For patients with existing kidney disease, the standard dosing of prochlorperazine (25 mg orally or by suppository, maximum three doses per 24 hours) can be followed without specific renal dose adjustments 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Nephrotoxicity of Antimicrobials and Antibiotics.

Advances in chronic kidney disease, 2020

Research

Antibiotic nephrotoxicity.

Chemioterapia : international journal of the Mediterranean Society of Chemotherapy, 1984

Research

Nephrotoxicity of antiinfective drugs.

International journal of clinical pharmacology and therapeutics, 1998

Research

Drug-Induced Nephrotoxicity and Dose Adjustment Recommendations: Agreement Among Four Drug Information Sources.

International journal of environmental research and public health, 2015

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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