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
125030712 12503071 2 F 20121122 20160707 20160628 20160714 EXP DE-ROCHE-1782167 ROCHE 79.00 YR F Y 50.00000 KG 20160714 MD DE DE

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
125030712 12503071 1 PS Rituximab RITUXIMAB 1 Intravenous (not otherwise specified) DATE OF LAST DOSE PRIOR TO SAE: 11/OCT/2012 103705 200 MG SOLUTION FOR INFUSION
125030712 12503071 2 SS BENDAMUSTINE BENDAMUSTINE 1 Intravenous (not otherwise specified) DATE OF LAST DOSE PRIOR TO SAE: 15/MAY/2012 0 124 MG INFUSION
125030712 12503071 3 C VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Unknown 0
125030712 12503071 4 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0 50 MG
125030712 12503071 5 C FUROSEMIDE. FUROSEMIDE 1 Unknown 0 80 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125030712 12503071 1 B-cell lymphoma
125030712 12503071 2 B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
125030712 12503071 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125030712 12503071 General physical health deterioration
125030712 12503071 Hepatic cirrhosis
125030712 12503071 Hepatitis B

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
125030712 12503071 1 20111215 0
125030712 12503071 2 20111215 0
125030712 12503071 3 20111223 0