What is the equivalent dose of hydromorphone (Hydromorph Contin) BID for a patient taking morphine (Contin) 100mg BID?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 24, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Converting Morphine Contin 100mg BID to Hydromorph Contin BID

For a patient taking morphine (Contin) 100mg BID (total 200mg/day oral morphine), convert to hydromorphone (Hydromorph Contin) using a 5:1 ratio, yielding 40mg/day oral hydromorphone, then reduce by 25-50% for incomplete cross-tolerance to arrive at 20-30mg/day hydromorphone, divided as 10-15mg BID. 1, 2

Step-by-Step Conversion Algorithm

Step 1: Calculate Total Daily Morphine Dose

  • The patient is taking 100mg BID = 200mg oral morphine per day 3

Step 2: Apply Morphine-to-Hydromorphone Conversion Ratio

  • Use a 5:1 conversion ratio (oral morphine to oral hydromorphone), which is the standard recommended by multiple guidelines 1, 4, 5, 6
  • The CDC conversion factor confirms hydromorphone is approximately 5 times more potent than morphine 3, 2
  • Calculation: 200mg morphine ÷ 5 = 40mg oral hydromorphone per day 1, 2

Step 3: Reduce for Incomplete Cross-Tolerance

  • Reduce the calculated dose by 25-50% to account for incomplete cross-tolerance when switching between opioids 1, 2
  • This yields: 40mg × 0.5 to 0.75 = 20-30mg hydromorphone per day 1
  • This critical step prevents overdosing during opioid rotation 1, 2

Step 4: Divide into BID Dosing

  • For BID administration: 20-30mg ÷ 2 = 10-15mg hydromorphone BID 1
  • Start at the lower end (10mg BID) if the patient had good pain control on morphine 1
  • Start at the higher end (15mg BID) if pain was poorly controlled on morphine 1

Breakthrough Pain Management

  • Provide immediate-release hydromorphone for breakthrough pain at 10-20% of the total daily dose 1
  • For a patient on 20-30mg/day total, breakthrough doses should be 2-4mg oral hydromorphone 1
  • Assess efficacy and side effects every 60 minutes after breakthrough dosing 1

Monitoring and Titration

  • Monitor closely after conversion for both pain control and adverse effects 2
  • If the patient requires more than 3 breakthrough doses per day, increase the scheduled dose rather than the frequency 1
  • Upward titration can be done after 24-48 hours if pain control is inadequate 1, 5

Critical Safety Considerations

  • Institute prophylactic bowel regimen with stimulant laxatives, as constipation is universal with opioid therapy 1
  • In renal impairment, reduce the calculated dose by an additional 25-50%, as hydromorphone exposure increases 2-3 fold in renal dysfunction 1
  • In hepatic impairment, reduce the calculated dose by an additional 25-50%, as exposure increases 4-fold in moderate hepatic impairment 1

Common Pitfalls to Avoid

  • Do not use a simple 1:5 ratio without dose reduction—this ignores incomplete cross-tolerance and risks overdosing 1, 2
  • Do not use conversion ratios of 1:8, which are too conservative and may lead to inadequate pain control; the 1:5 ratio with 25-50% reduction is the evidence-based approach 7, 5, 6
  • Avoid fixed conversion ratios without clinical judgment—consider patient-specific factors such as age, organ function, and prior pain control 1

References

Guideline

Hydromorphone Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Opioid Conversion Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Hydromorphone: pharmacology and clinical applications in cancer patients.

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2001

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.