Buy Prograf
Prograf

3.75
Prograf (tacrolimus) is an immunosuppressant used to prevent organ rejection in patients who have received a transplant. It works by lowering the body's immune system response to help the new organ stay healthy and function correctly.


Ingredient
Availability
In Stock
Delivery Time
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Tacrolimus
Reference Brand
Prograf
Manufacturer
Astellas Pharma
Product Form
Capsule, Granules, Injection, Ointment
Regulatory Classification
Rx
Primary Category
Immunosuppressant
Product Category
Antineoplastic and immunomodulating agents, Immunosuppressants, Calcineurin inhibitors
Pharmacological Class
Calcineurin Inhibitor
Manufacturer Description
A potent immunosuppressive drug used to prevent organ rejection after liver, kidney, or heart transplants.
Mechanism of Action
Tacrolimus suppresses the immune system by inhibiting the activation of T-lymphocytes, which are cells that would otherwise attack and reject a transplanted organ.
Route of Administration
Oral
Onset Time
1-3 days for therapeutic levels
Duration
12 hours
Contraindications
Hypersensitivity to macrolides, Pregnancy (unless essential)
Severe Adverse Events
Severe infections, Seizures, Kidney failure, Increased risk of lymphoma
Common Side Effects
Tremor, Headache, Nausea
Uncommon Side Effects
High blood pressure, Kidney function changes, Increased blood sugar, Insomnia
Drug Interactions
Grapefruit juice, St John’s Wort, Cyclosporine, Antifungals
Pregnancy Safety Warnings
Avoid unless potential benefit justifies the risk to the fetus.
Age Restrictions
Used in children under specialist guidance.
Storage Guidelines
Store at room temperature away from moisture.
Related Products
Cyclosporine, Adoport, Envarsus

Prograf FAQ

Can I travel internationally with Prograf, and will it affect airport security?

Yes, you can travel with Prograf. Carry the medication in its original prescription container, accompanied by a copy of the prescription or a doctor's letter. Airport security may inspect the medication, but it will not be restricted as a controlled substance in the UK.

Does Prograf have a distinctive appearance or imprint that helps identify it?

Prograf tablets are typically round, white (0.5 mg and 1 mg) or pink (5 mg), and are imprinted with “A-10” or “A-15” depending on the strength. Checking the imprint against the pharmacy label helps verify authenticity.

Will taking Prograf affect my ability to undergo drug testing for work or sport?

Tacrolimus can be detected in blood or urine but is not commonly screened for in standard occupational or sports drug tests. However, if a specific test for immunosuppressants is ordered, the presence of tacrolimus will be reported.

Are there any special considerations for pilots or airline crew taking Prograf?

Aviation medical authorities require that any medication potentially causing neuro-cognitive impairment be disclosed. Since tacrolimus can cause tremor or dizziness, pilots must be evaluated regularly and may need a medical exemption to continue flying.

What is the history behind the development of tacrolimus?

Tacrolimus was discovered in 1984 from the soil bacterium Streptomyces tsukubaensis in Japan. It was first approved for organ transplantation in the early 1990s and marketed as Prograf by Astellas Pharma.

How does Prograf compare to cyclosporine, another calcineurin inhibitor?

Both drugs inhibit calcineurin, but tacrolimus (Prograf) generally achieves similar immunosuppression at lower blood concentrations and may have a more favorable side-effect profile concerning gingival hyperplasia and hirsutism. Choice between them depends on individual response and tolerability.

Can I switch from a generic tacrolimus formulation to Prograf, or vice-versa?

Both contain the same active ingredient, but bioequivalence can vary. Switching should only occur under medical supervision, with close monitoring of trough levels to ensure consistent immunosuppression.

How stable is tacrolimus if I need to store it in a cooler environment, such as a travel cooler?

Tacrolimus is stable at room temperature. Prolonged exposure to temperatures below 15 °C or above 30 °C may affect tablet integrity. If stored in a cooler, keep it in a sealed container and avoid freezing.

Why does my insurance sometimes require prior authorization for Prograf?

Prograf is a high-cost, specialty medication used for transplant patients. UK NHS and private insurers often require clinical justification to ensure appropriate use before approving reimbursement.

What is Prograf?

Prograf is a prescription-only medication (POM) marketed in the United Kingdom by Astellas Pharma. Its sole active ingredient is tacrolimus, an immunosuppressant that belongs to the class of calcineurin inhibitors. Prograf is supplied as oral pills in strengths of 0.5 mg, 1 mg, and 5 mg. The drug is regulated by the Medicines and Healthcare products Regulatory Agency (MHRA) and is primarily used to prevent organ rejection after transplantation. Because tacrolimus modulates the immune system, it is occasionally considered for severe autoimmune conditions, but such uses are off-label in the UK.

How Prograf Works in the Body

Tacrolimus exerts its effect by binding to the intracellular protein FKBP-12 (FK506-binding protein). The tacrolimus-FKBP-12 complex then inhibits the enzyme calcineurin, a phosphatase essential for activating T-lymphocytes. By blocking calcineurin, tacrolimus reduces the production of interleukin-2 (IL-2) and other cytokines, thereby diminishing the proliferation and activation of T-cells that would otherwise attack a transplanted organ.

  • Onset of action: Blood levels rise within a few hours after a dose; immunosuppressive effect follows shortly thereafter.
  • Peak effect: Typically observed 1-3 hours post-dose.
  • Duration: The drug’s half-life is approximately 12 hours, requiring twice-daily dosing to maintain therapeutic trough concentrations.

Conditions Treated by Prograf

Approved (UK) indications

  • Prevention of organ rejection following kidney, liver, heart, or lung transplantation.
  • Adjunct therapy in bone-marrow transplantation (selected protocols).

These indications are supported by the MHRA and based on robust clinical trial data demonstrating reduced graft rejection rates when tacrolimus is part of a multi-drug immunosuppressive regimen.

Evidence-Based Off-Label Uses

Tacrolimus has been investigated for several severe autoimmune diseases, including:

  • Systemic lupus erythematosus (renal involvement) - small controlled trials suggest possible benefit when standard therapies fail.
  • Rheumatoid arthritis - case series report improvement in refractory cases.
  • Dermatologic autoimmune disorders (e.g., severe psoriasis) - oral tacrolimus is sometimes tried when topical preparations are insufficient.

Disclaimer: These uses are not approved by the MHRA. Off-label prescribing must be supervised by a specialist, and the risk-benefit profile should be assessed individually.

Who Should (Not) Use Prograf?

Ideal candidates

  • Adults undergoing solid-organ transplantation who require potent immunosuppression.
  • Patients whose baseline laboratory values (renal, hepatic, electrolytes) are within acceptable ranges and who can attend regular monitoring.

Absolute contraindications

  • Known hypersensitivity to tacrolimus or any component of the formulation.
  • Uncontrolled, severe infections (e.g., sepsis, active tuberculosis).
  • Pregnant women (tacrolimus is classified as Category C; potential fetal toxicity).

Relative contraindications & special considerations

  • Renal impairment: Dose reduction often needed; monitor creatinine closely.
  • Hepatic dysfunction: May increase drug levels; adjust dose as required.
  • Elderly: Increased sensitivity to neuro- and nephro-toxicity; start at the lower end of the dose range.
  • Breastfeeding: Tacrolimus passes into breast milk; avoidance is recommended.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Headache
  • Tremor or mild shakiness
  • Nausea, vomiting, or abdominal discomfort
  • Hypertension
  • Elevated blood glucose (possible new-onset diabetes)

These effects are usually dose-related and may improve with dose adjustment.

Serious Adverse Events

  • Nephrotoxicity: Rising serum creatinine, reduced glomerular filtration rate.
  • Infections: Opportunistic bacterial, viral (e.g., CMV), and fungal infections.
  • Malignancies: Increased risk of skin cancers and post-transplant lymphoproliferative disorder (PTLD).
  • Neurotoxicity: Severe tremor, seizures, or posterior reversible encephalopathy syndrome (PRES).
  • Hepatotoxicity: Elevated liver enzymes or cholestatic hepatitis.

If any of these occur, seek immediate medical attention.

Drug Interactions

  • CYP3A4 inhibitors (e.g., azole antifungals, macrolide antibiotics, diltiazem, verapamil) → increase tacrolimus levels → higher toxicity risk.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine, phenytoin, St John’s wort) → lower tacrolimus levels → risk of graft rejection.
  • Nephrotoxic agents (e.g., non-steroidal anti-inflammatory drugs, aminoglycosides) → additive kidney damage.

Patients should provide a full medication list-including over-the-counter products and herbal supplements-to their healthcare team.

Food and Lifestyle Interactions

  • Grapefruit juice markedly raises tacrolimus concentrations; avoidance is advised.
  • High-fat meals can increase absorption; take the medication consistently with regard to meals (same conditions each dose).
  • Alcohol may exacerbate liver toxicity; moderate consumption is recommended.
  • Driving or operating machinery: Tacrolimus can cause tremor or dizziness; use caution until individual response is known.

How to Take Prograf

  • Typical starting dose: 0.1 mg/kg body weight, administered twice daily (every 12 hours). The exact dose is individualized to achieve target blood trough levels (usually 5-15 ng/mL).
  • Available strengths: 0.5 mg, 1 mg, and 5 mg tablets. The prescribing clinician will select the combination that best matches the calculated dose.
  • Administration: Swallow whole with a glass of water. The pill may be taken with or without food, but maintain the same routine each day to avoid fluctuations in absorption.
  • Missed dose: Take the missed dose as soon as it is remembered unless the next scheduled dose is within 4 hours; in that case, skip the missed dose and continue the regular schedule. Do not double-dose.
  • Overdose: Symptoms may include severe tremor, confusion, seizures, and renal failure. Seek emergency medical care; treatment is supportive, and hemodialysis may be required in extreme cases.
  • Discontinuation: Abrupt cessation can precipitate acute rejection. Any dose reduction or withdrawal should be tapered under specialist supervision.

Monitoring and Follow-Up

  • Tacrolimus trough levels (blood concentration) measured 12 hours after the last dose, typically weekly during initiation, then every 1-3 months once stable.
  • Renal function: Serum creatinine and estimated glomerular filtration rate (eGFR) at each clinic visit.
  • Liver enzymes: ALT, AST, bilirubin to detect hepatotoxicity.
  • Blood pressure and glucose: Monitor weekly initially; adjust antihypertensive or antidiabetic therapy as needed.
  • Complete blood count: Periodic checks for anemia, leukopenia, or thrombocytopenia.

Regular follow-up appointments with the transplant or immunology team are essential to maintain therapeutic efficacy while minimizing toxicity.

Storage and Handling

  • Store tablets at room temperature (15 °C - 30 °C), away from moisture, light, and heat.
  • Keep the medication in the original container with a child-proof cap.
  • Do not use the product after the expiration date printed on the package.
  • Dispose of unused tablets according to local pharmacy return schemes or the UK’s NHS Drug Disposal guidelines.

Medication-Specific Glossary

Calcineurin
An intracellular phosphatase that activates T-cells; inhibition by tacrolimus suppresses immune responses.
Trough level
The lowest concentration of a drug in the bloodstream, measured just before the next dose; used to guide tacrolimus dosing.
Nephrotoxicity
Kidney damage caused by a medication, manifested as rising creatinine or reduced filtration.
CYP3A4
A liver enzyme that metabolises many drugs; tacrolimus is a substrate, so inhibitors or inducers of CYP3A4 change its blood levels.
Immunosuppression
Therapeutic reduction of the immune system’s activity to prevent graft rejection or control autoimmune disease.

Medical Disclaimer

This article provides educational information about Prograf and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Information for Prograf is sourced from established medical standards and updated frequently. It is provided for general guidance and should be confirmed with a healthcare professional before use.
Categories
Our Projects: Directory for Autoimmune Treatment Hong Kong - Tacrolimus Immunosuppressant Tablet