Mercaptopurine: Difference between revisions
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* Crohn's disease<ref name="pmid18666323">{{cite journal| author=Nagy F, Molnar T, Szepes Z, Farkas K, Nyari T, Lonovics J| title=Efficacy of 6-mercaptopurine treatment after azathioprine hypersensitivity in inflammatory bowel disease. | journal=World J Gastroenterol | year= 2008 | volume= 14 | issue= 27 | pages= 4342-6 | pmid=18666323 | doi= | pmc=PMC2731186 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18666323 }} </ref><ref name="pmid10566725">{{cite journal| author=Kim PS, Zlatanic J, Korelitz BI, Gleim GW| title=Optimum duration of treatment with 6-mercaptopurine for Crohn's disease. | journal=Am J Gastroenterol | year= 1999 | volume= 94 | issue= 11 | pages= 3254-7 | pmid=10566725 | doi=10.1111/j.1572-0241.1999.01532.x | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10566725 }} </ref> | * Crohn's disease<ref name="pmid18666323">{{cite journal| author=Nagy F, Molnar T, Szepes Z, Farkas K, Nyari T, Lonovics J| title=Efficacy of 6-mercaptopurine treatment after azathioprine hypersensitivity in inflammatory bowel disease. | journal=World J Gastroenterol | year= 2008 | volume= 14 | issue= 27 | pages= 4342-6 | pmid=18666323 | doi= | pmc=PMC2731186 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18666323 }} </ref><ref name="pmid10566725">{{cite journal| author=Kim PS, Zlatanic J, Korelitz BI, Gleim GW| title=Optimum duration of treatment with 6-mercaptopurine for Crohn's disease. | journal=Am J Gastroenterol | year= 1999 | volume= 94 | issue= 11 | pages= 3254-7 | pmid=10566725 | doi=10.1111/j.1572-0241.1999.01532.x | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10566725 }} </ref> | ||
* Non-Hodgkin's lymphoma<ref name="pmid7844597">{{cite journal| author=Reiter A, Schrappe M, Parwaresch R, Henze G, Müller-Weihrich S, Sauter S et al.| title=Non-Hodgkin's lymphomas of childhood and adolescence: results of a treatment stratified for biologic subtypes and stage--a report of the Berlin-Frankfurt-Münster Group. | journal=J Clin Oncol | year= 1995 | volume= 13 | issue= 2 | pages= 359-72 | pmid=7844597 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7844597 }} </ref><ref name="pmid3275750">{{cite journal| author=Hvizdala EV, Berard C, Callihan T, Falletta J, Sabio H, Shuster JJ et al.| title=Lymphoblastic lymphoma in children--a randomized trial comparing LSA2-L2 with the A-COP+ therapeutic regimen: a Pediatric Oncology Group Study. | journal=J Clin Oncol | year= 1988 | volume= 6 | issue= 1 | pages= 26-33 | pmid=3275750 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3275750 }} </ref><ref name="pmid1247950">{{cite journal| author=Wollner N, Burchenal JH, Lieberman PH, Exelby P, D'Angio G, Murphy ML| title=Non-Hodgkin's lymphoma in children. A comparative study of two modalities of therapy. | journal=Cancer | year= 1976 | volume= 37 | issue= 1 | pages= 123-34 | pmid=1247950 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1247950 }} </ref> | * Non-Hodgkin's lymphoma<ref name="pmid7844597">{{cite journal| author=Reiter A, Schrappe M, Parwaresch R, Henze G, Müller-Weihrich S, Sauter S et al.| title=Non-Hodgkin's lymphomas of childhood and adolescence: results of a treatment stratified for biologic subtypes and stage--a report of the Berlin-Frankfurt-Münster Group. | journal=J Clin Oncol | year= 1995 | volume= 13 | issue= 2 | pages= 359-72 | pmid=7844597 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7844597 }} </ref><ref name="pmid3275750">{{cite journal| author=Hvizdala EV, Berard C, Callihan T, Falletta J, Sabio H, Shuster JJ et al.| title=Lymphoblastic lymphoma in children--a randomized trial comparing LSA2-L2 with the A-COP+ therapeutic regimen: a Pediatric Oncology Group Study. | journal=J Clin Oncol | year= 1988 | volume= 6 | issue= 1 | pages= 26-33 | pmid=3275750 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3275750 }} </ref><ref name="pmid1247950">{{cite journal| author=Wollner N, Burchenal JH, Lieberman PH, Exelby P, D'Angio G, Murphy ML| title=Non-Hodgkin's lymphoma in children. A comparative study of two modalities of therapy. | journal=Cancer | year= 1976 | volume= 37 | issue= 1 | pages= 123-34 | pmid=1247950 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1247950 }} </ref> | ||
* Ulcerative colitis<ref name="pmid18666323">{{cite journal| author=Nagy F, Molnar T, Szepes Z, Farkas K, Nyari T, Lonovics J| title=Efficacy of 6-mercaptopurine treatment after azathioprine hypersensitivity in inflammatory bowel disease. | journal=World J Gastroenterol | year= 2008 | volume= 14 | issue= 27 | pages= 4342-6 | pmid=18666323 | doi= | pmc=PMC2731186 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18666323 }} </ref><ref name="pmid10566725">{{cite journal| author=Kim PS, Zlatanic J, Korelitz BI, Gleim GW| title=Optimum duration of treatment with 6-mercaptopurine for Crohn's disease. | journal=Am J Gastroenterol | year= 1999 | volume= 94 | issue= 11 | pages= 3254-7 | pmid=10566725 | doi=10.1111/j.1572-0241.1999.01532.x | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10566725 }} </ref><ref name="pmid8792685">{{cite journal| author=George J, Present DH, Pou R, Bodian C, Rubin PH| title=The long-term outcome of ulcerative colitis treated with 6-mercaptopurine. | journal=Am J Gastroenterol | year= 1996 | volume= 91 | issue= 9 | pages= 1711-4 | pmid=8792685 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8792685 }} </ref><ref name="pmid1972315">{{cite journal| author=Adler DJ, Korelitz BI| title=The therapeutic efficacy of 6-mercaptopurine in refractory ulcerative colitis. | journal=Am J Gastroenterol | year= 1990 | volume= 85 | issue= 6 | pages= 717-22 | pmid=1972315 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1972315 }} </ref> | |||
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Revision as of 20:52, 14 January 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rabin Bista, M.B.B.S. [2]
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Overview
Mercaptopurine is a Antineoplastic, antimetabolite that is FDA approved for the treatment of maintenance therapy of acute lymphatic (lymphocytic, lymphoblastic) leukemia as part of a combination regimen. Common adverse reactions include Bone marrrow toxicity, Hepatotoxicity, skin rashes, Diarrhoea, nausea, vomiting and anorexia.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Indication
- maintenance therapy of acute lymphatic (lymphocytic, lymphoblastic) leukemia as part of a combination regimen.
- The response to this agent depends upon the particular subclassification of acute lymphatic leukemia and the age of the patient (pediatric or adult).
Dosage
Maintenance Therapy
- Once a complete hematologic remission is obtained, maintenance therapy is considered essential. Maintenance doses will vary from patient to patient. The usual daily maintenance dose of mercaptopurine is 1.5 to 2.5 mg/kg/day as a single dose. It is to be emphasized that in pediatric patients with acute lymphatic leukemia in remission, superior results have been obtained when mercaptopurine has been combined with other agents (most frequently with methotrexate) for remission maintenance. Mercaptopurine should rarely be relied upon as a single agent for the maintenance of remissions induced in acute leukemia.
Dosage with Concomitant Allopurinol
- When allopurinol and mercaptopurine are administered concomitantly, the dose of mercaptopurine must be reduced to one third to one quarter of the usual dose to avoid severe toxicity.
Dosage in TPMT-deficient Patients
- Patients with inherited little or no thiopurine-S-methyltransferase (TPMT) activity are at increased risk for severe mercaptopurine toxicity from conventional doses of mercaptopurine and generally require substantial dose reduction. The optimal starting dose for homozygous deficient patients has not been established
Dosage in Renal and Hepatic Impairment
- It is probably advisable to start with lower dosages in patients with impaired renal function, due to slower elimination of the drug and metabolites and a greater cumulative effect. Consideration should be given to reducing the dosage in patients with impaired hepatic function.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Mercaptopurine in adult patients.
Non–Guideline-Supported Use
Indications
- Acute myeloid leukemia[1]
- Chronic myeloid leukemia
- Crohn's disease[2][3]
- Non-Hodgkin's lymphoma[4][5][6]
- Ulcerative colitis[2][3][7][8]
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
Condition1
- Dosing Information
- Dosage
Condition2
There is limited information regarding FDA-Labeled Use of Mercaptopurine in pediatric patients.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
Condition1
- Developed by:
- Class of Recommendation:
- Strength of Evidence:
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Guideline-Supported Use of Mercaptopurine in pediatric patients.
Non–Guideline-Supported Use
Condition1
- Dosing Information
- Dosage
Condition2
There is limited information regarding Off-Label Non–Guideline-Supported Use of Mercaptopurine in pediatric patients.
Contraindications
- Condition1
Warnings
- Description
Precautions
- Description
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Clinical Trial Experience of Mercaptopurine in the drug label.
Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous
Postmarketing Experience
There is limited information regarding Postmarketing Experience of Mercaptopurine in the drug label.
Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous
Drug Interactions
- Drug
- Description
Use in Specific Populations
Pregnancy
- Pregnancy Category
- Australian Drug Evaluation Committee (ADEC) Pregnancy Category
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Mercaptopurine in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Mercaptopurine during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Mercaptopurine with respect to nursing mothers.
Pediatric Use
There is no FDA guidance on the use of Mercaptopurine with respect to pediatric patients.
Geriatic Use
There is no FDA guidance on the use of Mercaptopurine with respect to geriatric patients.
Gender
There is no FDA guidance on the use of Mercaptopurine with respect to specific gender populations.
Race
There is no FDA guidance on the use of Mercaptopurine with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Mercaptopurine in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Mercaptopurine in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Mercaptopurine in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Mercaptopurine in patients who are immunocompromised.
Administration and Monitoring
Administration
- Oral
- Intravenous
Monitoring
There is limited information regarding Monitoring of Mercaptopurine in the drug label.
- Description
IV Compatibility
There is limited information regarding IV Compatibility of Mercaptopurine in the drug label.
Overdosage
Acute Overdose
Signs and Symptoms
- Description
Management
- Description
Chronic Overdose
There is limited information regarding Chronic Overdose of Mercaptopurine in the drug label.
Pharmacology
There is limited information regarding Mercaptopurine Pharmacology in the drug label.
Mechanism of Action
Structure
Pharmacodynamics
There is limited information regarding Pharmacodynamics of Mercaptopurine in the drug label.
Pharmacokinetics
There is limited information regarding Pharmacokinetics of Mercaptopurine in the drug label.
Nonclinical Toxicology
There is limited information regarding Nonclinical Toxicology of Mercaptopurine in the drug label.
Clinical Studies
There is limited information regarding Clinical Studies of Mercaptopurine in the drug label.
How Supplied
Storage
There is limited information regarding Mercaptopurine Storage in the drug label.
Images
Drug Images
{{#ask: Page Name::Mercaptopurine |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}
Package and Label Display Panel
{{#ask: Label Page::Mercaptopurine |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}
Patient Counseling Information
There is limited information regarding Patient Counseling Information of Mercaptopurine in the drug label.
Precautions with Alcohol
- Alcohol-Mercaptopurine interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
- ®[9]
Look-Alike Drug Names
- A® — B®[10]
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
- ↑ Canpolat C, Jeha S, Lockhart S, Ramirez I, Zipf T, Pinkel D (1997). "High-dose mercaptopurine and intermediate-dose cytarabine during first remission of acute myeloid leukemia". Cancer Invest. 15 (2): 121–6. PMID 9095207.
- ↑ 2.0 2.1 Nagy F, Molnar T, Szepes Z, Farkas K, Nyari T, Lonovics J (2008). "Efficacy of 6-mercaptopurine treatment after azathioprine hypersensitivity in inflammatory bowel disease". World J Gastroenterol. 14 (27): 4342–6. PMC 2731186. PMID 18666323.
- ↑ 3.0 3.1 Kim PS, Zlatanic J, Korelitz BI, Gleim GW (1999). "Optimum duration of treatment with 6-mercaptopurine for Crohn's disease". Am J Gastroenterol. 94 (11): 3254–7. doi:10.1111/j.1572-0241.1999.01532.x. PMID 10566725.
- ↑ Reiter A, Schrappe M, Parwaresch R, Henze G, Müller-Weihrich S, Sauter S; et al. (1995). "Non-Hodgkin's lymphomas of childhood and adolescence: results of a treatment stratified for biologic subtypes and stage--a report of the Berlin-Frankfurt-Münster Group". J Clin Oncol. 13 (2): 359–72. PMID 7844597.
- ↑ Hvizdala EV, Berard C, Callihan T, Falletta J, Sabio H, Shuster JJ; et al. (1988). "Lymphoblastic lymphoma in children--a randomized trial comparing LSA2-L2 with the A-COP+ therapeutic regimen: a Pediatric Oncology Group Study". J Clin Oncol. 6 (1): 26–33. PMID 3275750.
- ↑ Wollner N, Burchenal JH, Lieberman PH, Exelby P, D'Angio G, Murphy ML (1976). "Non-Hodgkin's lymphoma in children. A comparative study of two modalities of therapy". Cancer. 37 (1): 123–34. PMID 1247950.
- ↑ George J, Present DH, Pou R, Bodian C, Rubin PH (1996). "The long-term outcome of ulcerative colitis treated with 6-mercaptopurine". Am J Gastroenterol. 91 (9): 1711–4. PMID 8792685.
- ↑ Adler DJ, Korelitz BI (1990). "The therapeutic efficacy of 6-mercaptopurine in refractory ulcerative colitis". Am J Gastroenterol. 85 (6): 717–22. PMID 1972315.
- ↑ Empty citation (help)
- ↑ "http://www.ismp.org". External link in
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