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Mycophenolic Acid

Antimetabolite · Immunosuppressant

Also known as MYFORTIC, MPA, Mycophenolate mofetil, MMF, Ceptava, Mycophenolate Sodium

AntimetaboliteImmunosuppressant
CDSCO approved
EXCRETION
not curated
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Associated with congenital anomalies and increased risk of pregnancy loss. Women of childbearing potential must use effective contraception.
FDA category + note
Top interactionssee all 12
  • Activated CharcoalSevereDatabaseDDInter
  • AdalimumabSevereDatabaseDDInter
  • BaricitinibSevereDatabaseDDInter
  • CertolizumabSevereDatabaseDDInter

Mechanism

Mycophenolic acid (MPA) is an immunosuppressant that selectively and reversibly inhibits inosine monophosphate dehydrogenase (IMPDH), an enzyme crucial for the de novo synthesis of guanosine nucleotides. Lymphocytes are highly dependent on this pathway for proliferation and function, making them particularly susceptible to MPA's effects. This inhibition leads to a reduction in lymphocyte proliferation and antibody formation, thereby suppressing immune responses.

Indications

Prophylaxis of acute rejection in renal transplantation (in combination with a corticosteroid and ciclosporin)Prophylaxis of acute rejection in cardiac transplantation (in combination with ciclosporin and corticosteroids)Prophylaxis of acute rejection in hepatic transplantation (in combination with ciclosporin and corticosteroids)Prevention of transplant rejection

Dosing

Adult
For renal transplantation: 720 mg twice daily by mouth, to be started within 72 hours of transplantation.

Pharmacokinetics

Peak effect
Delayed due to enteric coating (for delayed-release tablet form).
Metabolism
Converted to MPAG.
Excretion
Metabolite (MPAG) undergoes tubular secretion.

Contraindications

  • Active serious gastro-intestinal disease (risk of haemorrhage, ulceration and perforation)
  • Use in children (due to higher incidence of side-effects)
  • Use in elderly (due to increased risk of infection, gastro-intestinal haemorrhage and pulmonary oedema)
  • Pregnancy (associated with congenital anomalies and increased risk of pregnancy loss)
  • Women of childbearing potential not using effective contraception

Side effects

Serious
  • Gastro-intestinal haemorrhage
  • Ulceration
  • Perforation
  • Increased risk of infection
  • Pulmonary oedema
  • Increased susceptibility to skin cancer
  • Hypogammaglobulinaemia
  • Bronchiectasis
  • Interstitial nephritis
  • Congenital anomalies (if used during pregnancy)
  • Pregnancy loss (if used during pregnancy)

Pregnancy & lactation

Pregnancy

Associated with congenital anomalies and increased risk of pregnancy loss. Women of childbearing potential must use effective contraception.

Drug interactions

Activated Charcoal
Severe
Database

Drug interaction classified as: absorption

Source: DDInter

Adalimumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Baricitinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Certolizumab
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Cholestyramine
Severe
Database

Drug interaction classified as: absorption

Source: DDInter

Cladribine
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Colesevelam
Severe
Database

Drug interaction classified as: absorption

Source: DDInter

Colestipol
Severe
Database

Drug interaction classified as: absorption

Source: DDInter

Deferiprone
Severe
Database

Clinical effect not specified

Source: DDInter

Dienogest
Severe
Database

Clinical effect not specified

Source: DDInter

Drospirenone
Severe
Database

Clinical effect not specified

Source: DDInter

Etanercept
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Related guidelines

Other Antimetabolite drugs

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Sources: Goodman & Gilman 14e, Katzung, BNF, Harriet Lane·Verified: 2026-05-10 · House clinical team