Azathioprine: Difference between revisions
Neil.m.young (talk | contribs) (Text replacement - "5 mg" to "5mg") |
Neil.m.young (talk | contribs) (Text replacement - "3 mg" to "3mg") |
||
| Line 7: | Line 7: | ||
==Adult Dosing== | ==Adult Dosing== | ||
===Kidney transplant rejection prophylaxis=== | ===Kidney transplant rejection prophylaxis=== | ||
*1- | *1-3mg/kg PO qd | ||
*Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary | *Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary | ||
| Line 24: | Line 24: | ||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===Kidney transplant rejection prophylaxis=== | ===Kidney transplant rejection prophylaxis=== | ||
*1- | *1-3mg/kg PO qd | ||
*Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary | *Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary | ||
Revision as of 11:12, 21 July 2016
Administration
- Type: immunosuppressant
- Dosage Forms: 50
- Routes of Administration: PO (IV form unavailable in US)
- Common Trade Names: Azasan, Imuran
Adult Dosing
Kidney transplant rejection prophylaxis
- 1-3mg/kg PO qd
- Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary
Rheumatoid arthritis, severe
- 1-2.5mg/kg/day PO divided qd-bid
- Start: 1mg/kg/day PO divided qd-bid; Max: 2.5mg/kg/day; Info: after 6-8wk may increase 0.5mg/kg/day q4wk
Crohns Disease
- 100-250mg PO qd
- Start: 50mg PO qd; Max: 2.5mg/kg/day; Info: for induction or remission maintenance and fistulizing disease, steroid-sparing effects
Ulcerative colitis
- 100-250mg PO qd
- Start: 50mg PO qd; Max: 2.5mg/kg/day; Info: for induction or remission maintenance, steroid-sparing effects
Pediatric Dosing
Kidney transplant rejection prophylaxis
- 1-3mg/kg PO qd
- Start: 3-5mg/kg PO x1 up to 3 days before transplant; Info: transplant protocols may vary
Juvenile idiopathic arthritis, severe
- 1-2.5mg/kg/day PO divided qd-bid
- Start: 1mg/kg/day PO divided qd-bid; Max: 2.5mg/kg/day; Info: after 6-8wk may increase 0.5mg/kg/day q4wk
Special Populations
- Pregnancy Rating: Pregnancy Category D
- Lactation risk: possibly unsafe
Renal Dosing
- Adult: CrCl 10-50: decrease dose 25%; CrCl <10: decrease dose 50%; HD: give 0.25mg/kg supplement; PD: not defined
- Pediatric: CrCl 10-50: decrease dose 25% or give q36h; CrCl <10: decrease dose 50% or give q48h; HD: give supplement; PD: not defined
Hepatic Dosing
- Adult: not defined; caution advised
- Pediatric: not defined; caution advised
Contraindications
- Allergy to class/drug
- pregnancy (RA use)
- caution if renal impairment
- caution if prior alkylating agents
Adverse Reactions
Serious
- leukopenia
- thrombocytopenia
- anemia
- myelosuppression
- immunosuppression
- infection
- PML
- GI hypersensitivity reaction
- pancreatitis
- hepatotoxicity
- hepatic veno-occlusive disease
- lymphoma
- malignancy
- acute febrile neutrophilic dermatosis
Common
- leukopenia
- thrombocytopenia
- anemia
- infection
- nausea
- vomiting
- anorexia
- diarrhea
- ALT, AST elevated
- malaise
- myalgia
- fever
- rash
- malignancy
Pharmacology
- Half-life: 5 hours
- Metabolism: liver extensively, erythrocytes; CYP450
- Excretion: bile, urine (1-2% unchanged)
Mechanism of Action
Acts as a prodrug for mercaptopurine, inhibiting an enzyme required for the synthesis of DNA. Thus, it most strongly affects proliferating cells, such as the T cells and B cells of the immune system
Comments
See Also
References
epocrates
