Mycophenolate Mofetil (CellCept)

Immunosuppressantprescriptionoral · inferred

Prodrug ester of mycophenolic acid (MPA), a selective reversible inhibitor of inosine-5'-monophosphate dehydrogenase (IMPDH) that depletes guanosine nucleotides preferentially in lymphocytes. First-line for solid-organ transplant maintenance immunosuppression (typically with tacrolimus + steroid taper) and for lupus nephritis, AIHA, myasthenia gravis, and other autoimmune conditions. Typical adult dose 500-1500 mg PO BID (2-3 g/day transplant). MMF is rapidly hydrolyzed to MPA (F~94%); MPA t1/2 ~18h with enterohepatic recirculation producing a secondary peak. GI toxicity (diarrhea, nausea) and myelosuppression are leading AEs; teratogenic, strict pregnancy prevention required (REMS).

Projected serum levels — 1k mg, twice daily

Mycophenolate Mofetil (CellCept) (precursor)Mycophenolic Acid
Mycophenolate Mofetil (CellCept) modeled serum levels, 1k mg twice daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 125 250 375 500 Day 0 Day 4 Day 7 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1
Mycophenolate Mofetil (CellCept) modeled serum levels with a loading dose of 1.4k mg, then 1k mg twice daily The first dose is larger so levels approach steady state faster. 0 125 250 375 500 Day 0 Day 4 Day 7 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 1k mg twice daily (oral).

Loading schedule: 1.4k mg on day 1, then 1k mg twice daily — reaching therapeutic levels sooner.

Modeled steady state after ~1 days: peak ≈ 190 mg, trough ≈ 0.000 mg body load. Population-based estimate over 15 days for a 1k mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Immunosuppressant
Route modeled
Oral
Model confidence
inferred
Half-life
18 h
Common dose
1k mg
Suggested maximum
3k mg/day
Reference dose range
500–3k mg (single dose)
Suggested cadence
twice daily
Validated against
1k mg oral — Cmax 24.5 mg/L at 1 h

Documented interactions

  • danger
    Levothyroxine (Synthroid) + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Levothyroxine (Synthroid) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • danger
    Tacrolimus (Prograf) + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Tacrolimus (Prograf) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • danger
    Warfarin (Coumadin) + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Warfarin (Coumadin) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • warning
    Apigenin + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Apigenin from plasma protein binding sites, transiently raising free drug concentration.

  • warning
    Aripiprazole (Abilify) + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Aripiprazole (Abilify) from plasma protein binding sites, transiently raising free drug concentration.

  • warning
    Armour Thyroid (Desiccated Thyroid Extract) + Mycophenolate Mofetil (CellCept) Protein binding

    Mycophenolate Mofetil (CellCept) may displace Armour Thyroid (Desiccated Thyroid Extract) from plasma protein binding sites, transiently raising free drug concentration.

Serum checks 143 modeled interaction pairings for mycophenolate mofetil (cellcept) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. Clinical pharmacokinetics of mycophenolate mofetil Bullingham RES, Nicholls AJ, Kamm BR · Clinical Pharmacokinetics, 1998 DOI

    Foundational PK review: MMF rapidly hydrolyzed to MPA (F~94%), MPA t1/2 ~18h, enterohepatic recirculation produces secondary peak, glucuronide metabolism dominates elimination.

  2. Therapeutic drug monitoring of mycophenolate mofetil in transplantation van Gelder T et al. · Therapeutic Drug Monitoring, 2006 DOI

    Consensus TDM guidance: MPA AUC 30-60 mg.h/L target in renal transplant, C0 trough targets, and PK variability justifying dose individualization.

2 published studies referenced in the app, each with a plain-language summary.