The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126280381 12628038 1 I 20160802 20160807 20160807 EXP PHHY2016CN107035 NOVARTIS LOU S, LUO Y, ZENG H, SHEN Y, ZHANG P, CHEN L ET.AL.,. ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION FOLLOWING DONOR CIK CELL INFUSION: A PHASE I STUDY IN PATIENTS WITH RELAPSED/REFRACTORY HEMATOLOGIC MALIGNANCIES. LEUKEMIA RESEARCH. 2016;48:6-10 27.00 YR M Y 0.00000 20160808 OT CN CN

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126280381 12628038 1 PS NEORAL CYCLOSPORINE 1 Intravenous (not otherwise specified) 2.5 MG, QD, DAY BEFORE TRANSPLANT 50716 2.5 MG SOLUTION QD
126280381 12628038 2 SS NEORAL CYCLOSPORINE 1 Oral 5 MG/KG, FOR 3-6 MONTHS 50716 5 MG/KG SOLUTION
126280381 12628038 3 SS NEORAL CYCLOSPORINE 1 50716 SOLUTION
126280381 12628038 4 SS SIMULECT BASILIXIMAB 1 Intravenous (not otherwise specified) 20 MG, ON THE DAY OF TRANSPLATION 0 20 MG VIAL
126280381 12628038 5 SS SIMULECT BASILIXIMAB 1 0 VIAL
126280381 12628038 6 SS SIMULECT BASILIXIMAB 1 0 VIAL
126280381 12628038 7 SS METHOTREXATE. METHOTREXATE 1 Intravenous (not otherwise specified) 15 MG/M2, DAY ONE AFTER TRANSPLANT 0 15 MG/M**2 SOLUTION FOR INJECTION
126280381 12628038 8 SS METHOTREXATE. METHOTREXATE 1 Intravenous (not otherwise specified) 10 MG/M2, HIRD DAY AFTER TRANSPLANT 0 10 MG/M**2 SOLUTION FOR INJECTION
126280381 12628038 9 SS METHOTREXATE. METHOTREXATE 1 0 SOLUTION FOR INJECTION
126280381 12628038 10 SS ANTITHYMOCYTE IMMUNOGLOBULIN THYMOCYTE IMMUNE GLOBULIN NOS 1 Intravenous drip 2.5 MG/KG, QD 0 2.5 MG/KG QD
126280381 12628038 11 SS ANTITHYMOCYTE IMMUNOGLOBULIN THYMOCYTE IMMUNE GLOBULIN NOS 1 0
126280381 12628038 12 SS ANTITHYMOCYTE IMMUNOGLOBULIN THYMOCYTE IMMUNE GLOBULIN NOS 1 0
126280381 12628038 13 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral 0.5 G, EVERY 12 H ON DAY 7 BEFORE TRANSPLANT 0 .5 G
126280381 12628038 14 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 0
126280381 12628038 15 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126280381 12628038 1 Stem cell transplant
126280381 12628038 2 Bone marrow transplant
126280381 12628038 3 Prophylaxis against graft versus host disease
126280381 12628038 4 Stem cell transplant
126280381 12628038 5 Bone marrow transplant
126280381 12628038 6 Prophylaxis against graft versus host disease
126280381 12628038 7 Stem cell transplant
126280381 12628038 8 Bone marrow transplant
126280381 12628038 9 Prophylaxis against graft versus host disease
126280381 12628038 10 Stem cell transplant
126280381 12628038 11 Bone marrow transplant
126280381 12628038 12 Prophylaxis against graft versus host disease
126280381 12628038 13 Stem cell transplant
126280381 12628038 14 Bone marrow transplant
126280381 12628038 15 Prophylaxis against graft versus host disease

Outcome of event

Event ID CASEID OUTC COD
126280381 12628038 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126280381 12628038 Cytomegalovirus infection
126280381 12628038 Neutropenia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found