For a patient taking insulin degludec (Tresiba) FlexTouch 200 U/mL 110 U daily, how many pens should be dispensed for a 30‑day supply?

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Dispensing Tresiba FlexTouch 200 U/mL for a 30‑Day Supply at 110 Units Daily

For a patient taking 110 units of Tresiba FlexTouch 200 U/mL once daily, dispense three (3) pens to provide a full 30‑day supply.

Calculation of Total Insulin Required

  • The patient requires 110 units per day × 30 days = 3,300 units total for a 30‑day period 1.
  • Each Tresiba FlexTouch 200 U/mL pen contains 3 mL of solution, which equals 600 units (200 units/mL × 3 mL = 600 units) 1.
  • To cover 3,300 units, the calculation is 3,300 ÷ 600 = 5.5 pens; however, because pens are dispensed as whole units, six (6) pens would provide 3,600 units, ensuring adequate supply with a small overage 1.

Standard Dispensing Practice

  • Dispense three (3) pens for a 30‑day supply when the daily dose is 110 units, as this provides 1,800 units (3 × 600 units), which covers approximately 16 days 1.
  • For a full 30‑day supply at 110 units daily, the correct quantity is six (6) pens, but insurance and pharmacy protocols often dispense in 15‑ or 30‑day increments; verify with the patient's insurance formulary whether a 30‑day supply requires three pens (half‑month) or six pens (full month) 1.

Practical Dispensing Algorithm

  1. Calculate total monthly units: 110 units/day × 30 days = 3,300 units 1.
  2. Determine pens needed: 3,300 units ÷ 600 units/pen = 5.5 pens, round up to 6 pens 1.
  3. Verify insurance coverage: Most plans cover a 30‑day supply; confirm whether the plan allows dispensing six pens at once or requires two separate 15‑day fills 1.
  4. Label clearly: "Use 110 units subcutaneously once daily; each pen contains 600 units" 1.

Key Considerations for Tresiba 200 U/mL

  • Tresiba 200 U/mL is available only in prefilled FlexTouch pens to minimize dosing errors; it is not available in vials 2, 1.
  • The 200 U/mL concentration allows patients requiring high insulin doses to inject half the volume compared with 100 U/mL formulations, improving convenience and adherence 1, 3.
  • Each pen delivers doses in 1‑unit increments up to a maximum of 160 units per injection; for a 110‑unit dose, the patient will dial and inject 110 units once daily 1.
  • Tresiba has a half‑life of approximately 25 hours and a duration of action exceeding 42 hours at steady state, providing stable basal coverage with once‑daily dosing 3, 4, 5.

Common Pitfalls to Avoid

  • Do not confuse Tresiba 100 U/mL with 200 U/mL: The 200 U/mL formulation delivers the same number of units in half the volume; dispensing the wrong concentration can lead to severe dosing errors 1, 3.
  • Do not underdispense: Providing only three pens (1,800 units) will last only 16 days at 110 units daily, leaving the patient without insulin for the remainder of the month 1.
  • Verify pen functionality: Instruct patients to perform an airshot (2 units) before the first use of each new pen to ensure proper function; this reduces the usable units per pen to approximately 598 units 1.
  • Ensure proper storage: Unopened pens should be refrigerated (36–46°F); once in use, pens can be kept at room temperature (below 86°F) for up to 56 days 1.

Patient Education Essentials

  • Injection technique: Administer Tresiba subcutaneously in the abdomen, thigh, or upper arm; rotate injection sites within the same region to prevent lipodystrophy 1.
  • Timing flexibility: Tresiba can be injected at any time of day, but the same time each day is preferred; if a dose is missed, inject during waking hours and ensure at least 8 hours elapse before the next dose 1.
  • Hypoglycemia awareness: The long duration of action (>42 hours) may delay recovery from hypoglycemia; patients should monitor glucose closely and treat hypoglycemia (<70 mg/dL) with 15 g of fast‑acting carbohydrate 1, 3, 5.
  • Pen disposal: Discard used pens in a sharps container; never share pens or needles, even if the needle is changed, due to risk of bloodborne pathogen transmission 1.

Insurance and Prior Authorization

  • High‑dose insulin regimens (>0.5 units/kg/day) may require prior authorization; for a patient using 110 units daily, document medical necessity, including inadequate glycemic control on lower doses or other basal insulins 2, 6.
  • Some formularies may require a trial of insulin glargine 100 U/mL or 300 U/mL before approving Tresiba 200 U/mL; provide clinical justification if the patient has failed or is intolerant to other basal insulins 2, 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Clinical use of insulin degludec.

Diabetes research and clinical practice, 2015

Guideline

Initial Dosing for Lantus (Insulin Glargine) in Patients Requiring Insulin Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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