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
126753061 12675306 1 I 20160810 20160813 20160822 20160822 EXP US-TAKEDA-2016MPI007236 TAKEDA 8.00 YR M Y 28.30000 KG 20160822 MD US US

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
126753061 12675306 1 PS VELCADE BORTEZOMIB 1 Intravenous (not otherwise specified) 1.3 MG/M2, UNK 21602 1.3 MG/M**2 INJECTION
126753061 12675306 2 SS VELCADE BORTEZOMIB 1 Intravenous (not otherwise specified) 1 MG, UNK 21602 1 MG INJECTION
126753061 12675306 3 SS CYTARABINE. CYTARABINE 1 Intrathecal UNK 0 INJECTION
126753061 12675306 4 SS Vincristine VINCRISTINE 1 Intravenous (not otherwise specified) 1.5 MG/M2, UNK 0 1.5 MG/M**2
126753061 12675306 5 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 3 MG/M2, UNK 0 3 MG/M**2
126753061 12675306 6 SS Daunorubicin DAUNORUBICIN 1 Intravenous (not otherwise specified) 25 MG, UNK 0 25 MG/M**2 INTRAVENOUS INFUSION
126753061 12675306 7 SS Pegaspargase PEGASPARGASE 1 Intravenous (not otherwise specified) 2500 UNK, UNK 0 2500 IU
126753061 12675306 8 SS METHOTREXATE. METHOTREXATE 1 Intrathecal UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126753061 12675306 1 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 3 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 4 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 5 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 6 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 7 Precursor T-lymphoblastic lymphoma/leukaemia
126753061 12675306 8 Precursor T-lymphoblastic lymphoma/leukaemia

Outcome of event

Event ID CASEID OUTC COD
126753061 12675306 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126753061 12675306 Abdominal pain
126753061 12675306 Constipation
126753061 12675306 Non-cardiac chest pain
126753061 12675306 Sinus tachycardia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126753061 12675306 1 20160718 20160730 0
126753061 12675306 3 20160718 20160718 0
126753061 12675306 4 20160718 20160808 0
126753061 12675306 5 20160718 20160809 0
126753061 12675306 6 20160718 20160808 0
126753061 12675306 7 20160718 20160804 0
126753061 12675306 8 20160718 20160725 0