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
125493022 12549302 2 F 2016 20160708 20160712 20160719 EXP US-CELGENEUS-USA-2016071994 CELGENE 0.00 F Y 0.00000 20160719 CN 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
125493022 12549302 1 PS THALOMID THALIDOMIDE 1 Oral U UNKNOWN 20785 50 MG CAPSULES QD
125493022 12549302 2 SS THALOMID THALIDOMIDE 1 Oral U UNKNOWN 20785 50 MG CAPSULES QD
125493022 12549302 3 SS POMALYST POMALIDOMIDE 1 Oral U 204026 4 MG CAPSULES QD
125493022 12549302 4 SS POMALYST POMALIDOMIDE 1 Oral U 204026 2 MG CAPSULES QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125493022 12549302 1 Plasma cell myeloma
125493022 12549302 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125493022 12549302 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125493022 12549302 Plasma cell myeloma

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
125493022 12549302 1 201102 0
125493022 12549302 2 201605 0
125493022 12549302 3 201505 0
125493022 12549302 4 201604 0