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
124599552 12459955 2 F 20160531 20160713 20160613 20160722 EXP US-JNJFOC-20160601779 JANSSEN 56.30 YR A F Y 58.00000 KG 20160722 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
124599552 12459955 1 PS DARATUMUMAB DARATUMUMAB 1 Intravenous (not otherwise specified) N 4370845 761036 CONCENTRATE FOR SOLUTION FOR INFUSION
124599552 12459955 2 SS DARATUMUMAB DARATUMUMAB 1 Intravenous (not otherwise specified) COMPLETED CYCLE 17 N 4370845 100638 940 MG CONCENTRATE FOR SOLUTION FOR INFUSION /month
124599552 12459955 3 SS VELCADE BORTEZOMIB 1 Subcutaneous COMPLETED CYCLE 8 N 0 2 MG LYOPHILIZED POWDER
124599552 12459955 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 10 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124599552 12459955 2 Plasma cell myeloma
124599552 12459955 3 Plasma cell myeloma
124599552 12459955 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
124599552 12459955 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124599552 12459955 Haemophilus bacteraemia
124599552 12459955 Upper respiratory tract infection

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
124599552 12459955 2 20150330 0
124599552 12459955 3 20150330 0
124599552 12459955 4 20150330 0