A complete drug profile of Tacrolimus an immunosuppressant used for organ transplant. It consist of PK/PD, MOA, Indication & Uses, Contraindications, Warnings & Precautions, Drug-interaction, Doses & Administration, Dosage forms, Chemical Formula, Side-Effects, Adverse Drug Reactions, Therapeutic Drug Monitoring (TDM).
2. Introduction
Tacrolimus, a macrolide immunosuppressant produced by
Streptomyces tsukubaensis.
Chemically, tacrolimus is designated as
[3S[3R*[E(1S*,3S*,4S*)],4S*,5R*,8S*,9E,12R*,14R*,15S*,16R*,1
8S*,19S*,26aR*]]5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-
hexadecahydro-5,19-dihydroxy3-[2-(4-hydroxy-3-
methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,
12,18-tetramethyl-8-(2-propenyl)-15,19-epoxy-3H-pyrido[2,1-
c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)
tetrone,monohydrate.
Tacrolimus has an empirical formula of C44H69NO12•H2O and
a formula weight of 822.03.
3. Indications & Uses
Tacrolimus is a calcineurin-inhibitor immunosuppressant indicated for
Prophylaxis of organ rejection in patients receiving allogeneic liver, kidney or
heart transplants
Use concomitantly with adrenal corticosteroids; in kidney and heart transplant,
use in conjunction with azathioprine or mycophenolate mofetil (MMF)
4. Limitations of Use
Do not use simultaneously with cyclosporine
Intravenous use reserved for patients who can not tolerate capsules orally
Use with sirolimus is not recommended in liver and heart transplant; use with
sirolimus in kidney transplant has not been established
6. Absorption
Tacrolimus, orally administrated, has a large variability in the rate of absorption
and absolute bioavailability which implies that the mean bioavailability is
approximately 25% but can range from 5% to 93%
Oral doses of tacrolimus should be 3 to 4 times higher than intravenous doses
to achieve comparable drug exposure after oral and intravenous administration.
In most patients tacrolimus is absorbed rapidly with peak plasma/blood
concentrations obtained in 0.5-1 hour32 however a lag time of 0 to 2 hours has
also been reported in some liver transplant recipients37 or an extended lag time
or secondary peaks
7. Distribution
Transplant recipients have significantly higher blood tacrolimus concentrations
(mean 15 times; range 4 to 114 times) than the corresponding plasma
concentrations due to the extensive binding of tacrolimus to the red blood cells.
The maximum amount of tacrolimus bound to red blood cells (bmax) is 418 ±
258 μg/l with an apparent dissociation constant (kd) of 3.8 ± 4.7 μg/l in
transplant patients while bmax is 1127 μg/l and KD of 13.5 μg/l in healthy
volunteers.
8. Metabolism
Tacrolimus undergoes O-demethylation, hydroxylation and/or oxidative
metabolic reactions, predominantly by CYP3A4 and CYP3A5 in the liver and
intestinal wall, with <0.5% of the parent drug appearing unchanged in the urine
or faeces.
Several metabolites are the product of a two-step reaction: oxidation by
cytochrome P450 3A enzymes destabilising the macrolide ring and followed by
its rearrangement.
9. Elimination
The metabolites of tacrolimus are for more than 95% eliminated by the biliary
route.
Urinary excretion accounts for, on average, 2.4% of tacrolimus elimination.
Biliary obstruction is reported to increase the concentration of tacrolimus
metabolites in the blood.
10. Mechanism of Action
It binds to an intracellular receptor and subsequently binds to calcineurin and
inhibits the calcineurin pathway that stimulates the nuclear factor, NFAT.
The action resembles that of cyclosporine (both drugs are calcineurin
inhibitors), although the cellular receptors differ.
By inhibiting the action of NFAT, tacrolimus decreases synthesis of
inflammatory cytokines.
In particular, synthesis of interleukin-2 (IL-2) is inhibited, which results in
decreased activation of T-lymphocytes.
It is 10-100 times more potent than cyclosporine.
Tacrolimus inhibits release of mast cell and basophil mediators and decreases
inflammatory mediator expression.
17. WARNINGS AND PRECAUTIONS
Lymphoma and Other Malignancies: Risk of lymphomas, including post
transplant lymphoproliferative disorder (PLTD); appears related to intensity and
duration of use. Avoid prolonged exposure to UV light and sunlight.
Serious infections: Increased risk of bacterial, viral, fungal and protozoal
infections, including opportunistic infections: combination immunosuppression
should be used with caution.
Polyoma Virus Infections: Serious, sometimes fatal outcomes, including
polyoma virus-associated nephropathy (PVAN), mostly due to BK virus, and JC
virus-associated progressive multifocal leukoencephalopathy (PML); consider
reducing immunosuppression
18. WARNINGS AND PRECAUTIONS
Cytomegalovirus (CMV) Infections: Increased risk of CMV viremia and disease;
consider reducing immunosuppression.
New Onset Diabetes After Transplant: Monitor blood glucose.
Nephrotoxicity: Acute and/or chronic; reduce the dose; use caution with other
nephrotoxic drugs
Neurotoxicity: Risk of Posterior Reversible Encephalopathy Syndrome, monitor
for neurologic abnormalities; reduce or discontinue Prograf and other
immunosuppressants.
Hyperkalemia: Monitor serum potassium levels. Careful consideration should
be given prior to use of other agents also associated with hyperkalemia.
19. WARNINGS AND PRECAUTIONS
Hypertension: May require antihypertensive therapy. Monitor relevant drug-
drug interactions
Anaphylactic Reactions with IV formulation: Observe patients receiving
tacrolimus injection for signs and symptoms of anaphylaxis
Use with Sirolimus: Not recommended in liver and heart transplant due to
increased risk of serious adverse reactions.
Myocardial Hypertrophy: Consider dosage reduction or discontinuation.
Immunizations: Use of live vaccines should be avoided.
Pure Red Cell Aplasia: Discontinuation should be considered.
20. DRUG INTERACTIONS
Mycophenolic Acid Products: Can increase MPA exposure after crossover from
cyclosporine to Prograf; monitor for MPA-related adverse reactions and adjust
MMF or MPA-dose as needed
Nelfinavir and Grapefruit Juice: Increased tacrolimus concentrations via CYP3A
inhibition; avoid concomitant use
CYP3A Inhibitors: Increased tacrolimus concentrations; monitor concentrations
and adjust tacrolimus dose as needed with concomitant use
CYP3A4 Inducers: Decreased tacrolimus concentrations; monitor
concentrations and adjust tacrolimus dose as needed with concomitant use
21. USE IN SPECIFIC POPULATIONS
Pregnancy: Based on animal data may cause fetal harm. Use only if the
potential benefit justifies the risk.
Nursing Mothers: Discontinue nursing taking into consideration importance of
drug to mother.
Hepatic/Renal impaired patients: Administer at the lower end of the
recommended starting dose. Monitor renal function in patients with impaired
renal function.
22. Therapeutic Drug Monitoring (TDM)
Tacrolimus has a narrow therapeutic index and highly variable pharmacokinetic
characteristics.
Close monitoring of the tacrolimus concentration is required to achieve an
optimal efficiency and thus minimizing the risk of subtherapeutic or toxic blood
concentrations.
Efficacy and side effects of tacrolimus are highly correlated with the area under
the curve (AUC0-12)
The most exact way to monitor the total tacrolimus exposure is by creating 12
hour pharmacokinetic profiles, which implicates that the tacrolimus
concentration should be measured at at least 6 different time points.
23. Therapeutic Drug Monitoring (TDM)
The AUC0-12 can then be calculated according to the trapezoidal rule using the
tacrolimus concentrations measured at different time points.
Since recording a complete 12 hour pharmacokinetic profile for every patient is
not feasible in clinical practice, traditionally many transplant centres use
tacrolimus trough (C0) concentrations to estimate the tacrolimus exposure.
Although tacrolimus C0 concentrations are generally considered to be a good
indication of the total systemic drug exposure its usefulness in differentiating
graft rejection episodes from nephrotoxicity has been questioned.
24. Therapeutic Drug Monitoring (TDM)
Based on the half-life of tacrolimus which is approximately ten hours, it is
necessary to wait at least 36 hours (3.3 half-lives) to reach a steady state
tacrolimus concentration after initiation of therapy or after a change in the
administration regime of tacrolimus.
Ideally, after starting the infusion, blood concentrations should be monitored
on day 2 or 3 on average 3 to 7 times weekly during the first few weeks after
transplantation, and less frequently thereafter.
Special circumstances such as changes in liver function, presence of adverse
effects or use of drugs that may alter tacrolimus kinetics may warrant more
frequent monitoring.