What is the dosing difference between Advagraf (tacrolimus) and Pangraf (tacrolimus) for post-transplant immunosuppression?

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Last updated: June 18, 2025View editorial policy

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From the Guidelines

The main dosing difference between Advagraf and Pangraf is that Advagraf is a once-daily extended-release tacrolimus formulation, while Pangraf is typically administered twice daily. For post-transplant immunosuppression, Advagraf is taken once every 24 hours, usually in the morning, whereas Pangraf requires dosing every 12 hours. When converting from Pangraf to Advagraf, the total daily dose remains the same, but is consolidated into a single administration. For example, a patient taking 2 mg of Pangraf twice daily (4 mg total) would take 4 mg of Advagraf once daily. Both medications contain the same active ingredient (tacrolimus) and provide similar overall immunosuppression, but Advagraf's extended-release formulation maintains therapeutic blood levels over 24 hours with a single dose.

This difference in dosing frequency can improve medication adherence for transplant patients who must take immunosuppressants lifelong. Blood level monitoring remains essential for both formulations, with target trough levels typically ranging from 5-15 ng/mL depending on transplant type, time post-transplant, and individual patient factors, as recommended by the EASL clinical practice guidelines on liver transplantation 1. Patients should take either medication consistently with respect to meals, as food can affect tacrolimus absorption.

Some key considerations for dosing include:

  • Tacrolimus trough levels should be kept at 6-10 ng/ml during the first month followed by 4-8 ng/ml thereafter, as recommended by the EASL guidelines 1
  • It is recommended to combine tacrolimus with other immunosuppressive drugs to allow for a lower range of tacrolimus trough levels and to help preserve renal function 1
  • The administration of basiliximab induction with delayed introduction of tacrolimus is strongly recommended in patients at risk of developing post-transplant renal dysfunction 1
  • Exposure to CNIs should be minimised by employing combined immunosuppressive regimens, preferably an mTORi in the case of high risk of hepatic or extrahepatic cancer recurrence 1.

Overall, the choice between Advagraf and Pangraf should be based on individual patient factors, including medication adherence and side effect profiles, with the goal of achieving optimal immunosuppression and minimizing adverse effects, as supported by the EASL clinical practice guidelines on liver transplantation 1.

From the FDA Drug Label

The provided drug labels do not contain direct information comparing the dosing of Advagraf (tacrolimus) and Pangraf (tacrolimus) for post-transplant immunosuppression.

The FDA drug label does not answer the question.

From the Research

Dosing Difference Between Advagraf and Pangraf

The dosing difference between Advagraf (tacrolimus) and Pangraf (tacrolimus) for post-transplant immunosuppression is not explicitly stated in the provided studies, as Pangraf is not mentioned. However, the studies provide information on the dosing of Advagraf compared to Prograf (another formulation of tacrolimus).

Key Findings

  • Advagraf is a once-daily formulation of tacrolimus, while Prograf is a twice-daily formulation 2, 3.
  • De novo kidney transplant recipients may need higher doses of Advagraf compared to Prograf to achieve therapeutic levels 4.
  • The switch from Prograf to Advagraf can result in a sustained decrease in tacrolimus exposure, requiring close medical supervision 5.
  • The dose ratio of Prograf to Advagraf is often 1:1, but patients may require higher doses of Advagraf to maintain stable renal function 6.

Dosing Considerations

  • The required daily doses of tacrolimus may increase when switching from Prograf to Advagraf 5.
  • Tacrolimus trough levels may decrease after conversion to Advagraf, requiring dose adjustments 5.
  • The use of Advagraf may offer benefits such as improved adherence and a safer profile by avoiding toxic peak concentrations 3, 5.

Study Limitations

  • The studies provided do not directly compare Advagraf to Pangraf, making it difficult to determine the dosing difference between the two formulations.
  • The studies have varying sample sizes, study designs, and follow-up periods, which may limit the generalizability of the findings 2, 3, 6, 4, 5.

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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