Tacrolimus: Difference between revisions
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==Adult Dosing== | ==Adult Dosing== | ||
===Heart transplant rejection prophylaxis=== | ===Heart transplant rejection prophylaxis=== | ||
*0. | *0.075mg/kg/day PO divided q12h | ||
*Start: >6h post-transplant; Info: adjust dose based on serum levels | *Start: >6h post-transplant; Info: adjust dose based on serum levels | ||
===Liver transplant rejection prophylaxis=== | ===Liver transplant rejection prophylaxis=== | ||
*0.1-0. | *0.1-0.15mg/kg/day PO divided q12h | ||
*Start: >6h post-transplant; Info: adjust dose based on serum levels | *Start: >6h post-transplant; Info: adjust dose based on serum levels | ||
===Kidney transplant rejection prophylaxis=== | ===Kidney transplant rejection prophylaxis=== | ||
*0.1-0. | *0.1-0.2mg/kg/day PO divided q12h | ||
*Start: | *Start: within 24h post-transplant; delay if renal function not adequate; Info: adjust dose based on serum levels | ||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===Liver transplant rejection prophylaxis=== | |||
*0.15-0.2mg/kg/day PO divided q12h | |||
*Start: >6h post-transplant; Info: adjust dose based on serum levels | |||
==Special Populations== | ==Special Populations== | ||
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: Pregnancy Category C | ||
*[[Lactation risk categories|Lactation risk]]: | *[[Lactation risk categories|Lactation risk]]: possibly unsafe | ||
===Renal Dosing=== | ===Renal Dosing=== | ||
*Adult: | *Adult: | ||
*Pediatric: | **kidney transplant: give lowest recommended dose, may consider further dose decrease; postop oliguria: start 6-24h post-transplant; may delay until renal function adequate; HD: not defined | ||
**all other transplants: give lowest recommended dose, may consider further dose decrease; HD: not defined | |||
*Pediatric: give lowest recommended dose, may consider further dose decrease; HD: not defined | |||
===Hepatic Dosing=== | ===Hepatic Dosing=== | ||
*Adult: | *Adult: give lowest recommended dose, may consider further dose decrease; Child-Pugh Score >10: decrease dose, amount not defined | ||
*Pediatric: | *Pediatric: give lowest recommended dose, may consider further dose decrease; Child-Pugh Score >10: decrease dose, amount not defined | ||
==Contraindications== | ==Contraindications== | ||
*Allergy to class/drug | *Allergy to class/drug | ||
*hypersensitivity to castor oil derivatives (IV form) | |||
*liver transplant use (ER cap form) | |||
*electrolyte abnormalities, uncorrected | |||
*congenital long QT syndrome | |||
*caution if QT prolongation | |||
*caution if [[QT prolongation]] family history | |||
*caution if torsades de pointes history | |||
*caution if ventricular arrhythmias | |||
*caution if bradycardia | |||
*caution if recent MI | |||
*caution if CHF | |||
*caution in female patients | |||
*caution in Black patients | |||
*caution in Hispanic patients | |||
*caution if renal impairment | |||
*caution if hepatic impairment | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*immunosuppression | |||
*malignancy | |||
*lymphoma | |||
*post-transplant lymphoproliferative disorder | |||
*infection, severe | |||
*CMV | |||
*PML | |||
*BK virus-assoc. nephropathy | |||
*Stevens-Johnson syndrome | |||
*toxic epidermal necrolysis | |||
*anaphylaxis | |||
*nephrotoxicity | |||
*neurotoxicity | |||
*posterior reversible encephalopathy syndrome | |||
*seizures | |||
*myocardial hypertrophy | |||
*pericardial effusion | |||
*QT prolongation | |||
*torsades de pointes | |||
*hyperkalemia, severe | |||
*hypertension, severe | |||
*diabetes mellitus | |||
*myelosuppression | |||
*DIC | |||
*thrombocytopenic purpura | |||
*hemolytic anemia | |||
*pure red cell aplasia | |||
===Common=== | ===Common=== | ||
*tremor | |||
*diarrhea | |||
*headache | |||
*hypertension | |||
*Creatinine increase | |||
*infection | |||
*nausea/vomiting | |||
*insomnia | |||
*pain | |||
*hypophosphatemia | |||
*constipation | |||
*asthenia | |||
*edema, peripheral | |||
*hypomagnesemia | |||
*fever | |||
*anemia | |||
*diabetes mellitus/hyperglycemia | |||
*paresthesia | |||
*LFTs elevated | |||
*hyperlipidemia | |||
*hyperkalemia | |||
*anorexia | |||
*dyspepsia | |||
*arthralgia | |||
*dyspnea | |||
*pruritus/rash | |||
*hypokalemia | |||
*dizziness | |||
*cough | |||
*leukopenia | |||
*photosensitivity | |||
*bronchitis | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 3.5-40.6h; 23.6h (heart transplant patients), 18.8h (kidney transplant patients), 11.7h (liver transplant patients); Info: prolonged half-life in hepatic impairment | ||
*Metabolism: | *Metabolism: liver extensively; CYP450: 3A4 substrate | ||
*Excretion: | *Excretion:feces 92.4%, urine 2.3% (<1% unchanged) | ||
==Mechanism of Action== | ==Mechanism of Action== | ||
Macrolide calcineurin inhibitor, inhibits T-lymphocyte activation | |||
==Comments== | ==Comments== | ||
==See Also== | ==See Also== | ||
*[[Transplant complications]] | |||
*[[Immunocompromised antibiotics]] | |||
==References== | ==References== | ||
<references/> | <references/> | ||
[[Category: | [[Category:Pharmacology]] | ||
epocrates | |||
Latest revision as of 20:00, 8 March 2021
Administration
- Type: immunosuppressant
- Dosage Forms: 0.5,1,5
- Routes of Administration: PO, topical, IV
- Common Trade Names:Prograf
Adult Dosing
Heart transplant rejection prophylaxis
- 0.075mg/kg/day PO divided q12h
- Start: >6h post-transplant; Info: adjust dose based on serum levels
Liver transplant rejection prophylaxis
- 0.1-0.15mg/kg/day PO divided q12h
- Start: >6h post-transplant; Info: adjust dose based on serum levels
Kidney transplant rejection prophylaxis
- 0.1-0.2mg/kg/day PO divided q12h
- Start: within 24h post-transplant; delay if renal function not adequate; Info: adjust dose based on serum levels
Pediatric Dosing
Liver transplant rejection prophylaxis
- 0.15-0.2mg/kg/day PO divided q12h
- Start: >6h post-transplant; Info: adjust dose based on serum levels
Special Populations
- Pregnancy Rating: Pregnancy Category C
- Lactation risk: possibly unsafe
Renal Dosing
- Adult:
- kidney transplant: give lowest recommended dose, may consider further dose decrease; postop oliguria: start 6-24h post-transplant; may delay until renal function adequate; HD: not defined
- all other transplants: give lowest recommended dose, may consider further dose decrease; HD: not defined
- Pediatric: give lowest recommended dose, may consider further dose decrease; HD: not defined
Hepatic Dosing
- Adult: give lowest recommended dose, may consider further dose decrease; Child-Pugh Score >10: decrease dose, amount not defined
- Pediatric: give lowest recommended dose, may consider further dose decrease; Child-Pugh Score >10: decrease dose, amount not defined
Contraindications
- Allergy to class/drug
- hypersensitivity to castor oil derivatives (IV form)
- liver transplant use (ER cap form)
- electrolyte abnormalities, uncorrected
- congenital long QT syndrome
- caution if QT prolongation
- caution if QT prolongation family history
- caution if torsades de pointes history
- caution if ventricular arrhythmias
- caution if bradycardia
- caution if recent MI
- caution if CHF
- caution in female patients
- caution in Black patients
- caution in Hispanic patients
- caution if renal impairment
- caution if hepatic impairment
Adverse Reactions
Serious
- immunosuppression
- malignancy
- lymphoma
- post-transplant lymphoproliferative disorder
- infection, severe
- CMV
- PML
- BK virus-assoc. nephropathy
- Stevens-Johnson syndrome
- toxic epidermal necrolysis
- anaphylaxis
- nephrotoxicity
- neurotoxicity
- posterior reversible encephalopathy syndrome
- seizures
- myocardial hypertrophy
- pericardial effusion
- QT prolongation
- torsades de pointes
- hyperkalemia, severe
- hypertension, severe
- diabetes mellitus
- myelosuppression
- DIC
- thrombocytopenic purpura
- hemolytic anemia
- pure red cell aplasia
Common
- tremor
- diarrhea
- headache
- hypertension
- Creatinine increase
- infection
- nausea/vomiting
- insomnia
- pain
- hypophosphatemia
- constipation
- asthenia
- edema, peripheral
- hypomagnesemia
- fever
- anemia
- diabetes mellitus/hyperglycemia
- paresthesia
- LFTs elevated
- hyperlipidemia
- hyperkalemia
- anorexia
- dyspepsia
- arthralgia
- dyspnea
- pruritus/rash
- hypokalemia
- dizziness
- cough
- leukopenia
- photosensitivity
- bronchitis
Pharmacology
- Half-life: 3.5-40.6h; 23.6h (heart transplant patients), 18.8h (kidney transplant patients), 11.7h (liver transplant patients); Info: prolonged half-life in hepatic impairment
- Metabolism: liver extensively; CYP450: 3A4 substrate
- Excretion:feces 92.4%, urine 2.3% (<1% unchanged)
Mechanism of Action
Macrolide calcineurin inhibitor, inhibits T-lymphocyte activation
Comments
See Also
References
epocrates
