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
125702971 12570297 1 I 20151201 20160714 20160719 20160719 PER US-TAKEDA-2016MPI006432 TAKEDA 68.56 YR F Y 0.00000 20160719 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
125702971 12570297 1 PS VELCADE BORTEZOMIB 1 Unknown UNK Y 21602 INJECTION
125702971 12570297 2 SS REVLIMID LENALIDOMIDE 1 Oral 15 MG, QD Y A0480F 0 15 MG QD
125702971 12570297 3 SS REVLIMID LENALIDOMIDE 1 Oral 10 MG, QD Y A0480F 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125702971 12570297 1 Product used for unknown indication
125702971 12570297 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125702971 12570297 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125702971 12570297 Abdominal pain
125702971 12570297 Anaemia

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
125702971 12570297 2 20151123 20160314 0
125702971 12570297 3 20160314 0