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
103698812 10369881 2 F 201402 20160726 20140808 20160727 EXP FR-ROCHE-1446833 ROCHE 59.00 YR M Y 0.00000 20160727 MD FR FR

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
103698812 10369881 1 PS MABTHERA RITUXIMAB 1 Unknown U 103705
103698812 10369881 2 SS ENDOXAN CYCLOPHOSPHAMIDE 1 Unknown U 0
103698812 10369881 3 SS EMEND APREPITANT 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103698812 10369881 1 Waldenstrom's macroglobulinaemia
103698812 10369881 2 Waldenstrom's macroglobulinaemia
103698812 10369881 3 Vomiting

Outcome of event

Event ID CASEID OUTC COD
103698812 10369881 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103698812 10369881 Gait disturbance
103698812 10369881 Paraesthesia
103698812 10369881 Tinnitus

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
103698812 10369881 1 201312 0
103698812 10369881 2 201312 0
103698812 10369881 3 201312 0