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
125951971 12595197 1 I 20150405 20160718 20160727 20160727 EXP CN-TAKEDA-2016MPI006660 TAKEDA 66.00 YR M Y 68.00000 KG 20160726 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
125951971 12595197 1 PS VELCADE BORTEZOMIB 1 Subcutaneous 2.38 MG, UNK U 140410454 21602 2.38 MG INJECTION
125951971 12595197 2 SS VELCADE BORTEZOMIB 1 Subcutaneous 2.38 MG, UNK U 140410454 21602 2.38 MG INJECTION
125951971 12595197 3 SS VELCADE BORTEZOMIB 1 Subcutaneous 2.38 MG, UNK U 140410454 21602 2.38 MG INJECTION
125951971 12595197 4 SS PREDNISONE. PREDNISONE 1 Oral 100 MG, UNK U 0 100 MG TABLET
125951971 12595197 5 SS PREDNISONE. PREDNISONE 1 Oral 100 MG, UNK U 0 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125951971 12595197 1 Lymphoma
125951971 12595197 4 Mantle cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
125951971 12595197 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125951971 12595197 Abdominal distension
125951971 12595197 Diarrhoea
125951971 12595197 Hypoaesthesia
125951971 12595197 Nausea
125951971 12595197 Pain

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
125951971 12595197 1 20150408 0
125951971 12595197 2 20150401 0
125951971 12595197 3 20150404 0
125951971 12595197 4 20150401 0
125951971 12595197 5 20150404 0