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New search Medicine profile Mycophenolate Mofetil

Clinical medicine profile

Mycophenolate Mofetil

Therapeutic agent (verify pharmacological class)

POM
Evidence state General guidance Reviewed 14 Aug 2026
Route
See product SmPC
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

Some sections contain general class guidance rather than medicine-specific evidence. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • Hypersensitivity to the active substance or excipients.
  • Additional absolute contraindications are indication- and product-specific — consult SmPC.

Precautions

  • GIT diseases
  • live attenuated vaccines
  • complete blood count performed as follows - weekly during the 1st month, twice monthly for the 2nd and the 3rd month of treatment, then monthly through the 1st yr
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

Cardiac:1.5 gm BD [in combination with cyclosporine and corticosteroids]. Renal: 1 gm BD in combination with cyclosporine and corti- costeroids].

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Review renal impairment dosing; many agents need CrCl/eGFR adjustment.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.
Hepatic

Review hepatic impairment dosing; monitor LFTs if agent is hepatically cleared or hepatotoxic.

03 Clinical use

Use, effects & interactions

Indications

  • Prophylaxis of acute renal or cardiac transplant rejection.
  • It is used in combination with cyclosporine and corticosteroids.
  • Clinical selection for Mycophenolate Mofetil should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Therapeutic agent (verify pharmacological class).
  • Confirm site-specific dose, duration and monitoring before prescribing.

Adverse effects

  • chest pain
  • dysp- nea
  • hematuria
  • hypertension
  • leukopenia
  • neu- tropenia
  • infections
  • peripheral edema
  • arthralgia joint pain
  • GI haemorrhage
  • gingival hyperplasia
  • neutropenia
  • oral moniliasis
  • pancreatitis
  • Professional use: confirm indication, dose, duration, monitoring and patient counselling points against current Kenya STG / EML and the product SmPC.
  • Document allergy status and key interactions.
04 Pharmacology

Mechanism & disposition

It is metabolized to mycophenolic acid, which is a selective, noncompetitive, and reversible inhibitor of inosine monophosphate dehydrogenase.

It is metabolized to mycophenolic acid, wh…The de novo synthesis pathway of guanosine…Its selectivity is due to the fact that T…
Read complete mechanism

It is metabolized to mycophenolic acid, which is a selective, noncompetitive, and reversible inhibitor of inosine monophosphate dehydrogenase. The de novo synthesis pathway of guanosine nucleotides is inhibited without being incorporated into DNA. Its selectivity is due to the fact that T and B-lymphocytes are almost solely dependent for their proliferation on the inhibited de novo synthesis of purines, while other cell types can utilize salvage pathways.

Onset

Product-specific

Duration

Product-specific

Route

See product SmPC

Elimination

are product-specific. Consider food effects, protein binding, hepatic CYP/UGT

Half-life

when adjusting for organ impairment, age and drug interactions. Verify parameters in the current SmPC.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Use only if potential benefit justifies potential risk; prefer agents with better reproductive data when alternatives exist.

Lactation

Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data.

06 Kenya market

Brands & loaded prices

From
Median
Listings2
BrandManufacturerPackObserved price
Mofecon-C 250 Concord Biotech LTD. Capsule, Hard Unavailable
PHENOLATE TABLETS MEDCURE HEALTHCARE LTD Tablet Unavailable
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Professional class pharmacology (Therapeutic agent (verify pharmacological class))
Last reviewed14 Aug 2026
EvidenceGeneral guidance
Open source document ↗

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.