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
123108332 12310833 2 F 20160314 20160707 20160427 20160720 EXP GB-CELGENEUS-GBR-2016037644 CELGENE 68.82 YR F Y 92.50000 KG 20160720 MD GB GB

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
123108332 12310833 1 PS CC-4047 POMALIDOMIDE 1 Oral U 66188 4 MG CAPSULES
123108332 12310833 2 SS CC-4047 POMALIDOMIDE 1 Oral U 66188 4 MG CAPSULES
123108332 12310833 3 SS CC-4047 POMALIDOMIDE 1 Oral U 66188 4 MG CAPSULES
123108332 12310833 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 0 40 MG UNKNOWN
123108332 12310833 5 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 0 40 MG UNKNOWN
123108332 12310833 6 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 0 40 MG UNKNOWN
123108332 12310833 7 C rivaroxaban RIVAROXABAN 1 Oral 0 10 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123108332 12310833 1 Plasma cell myeloma
123108332 12310833 4 Plasma cell myeloma
123108332 12310833 7 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
123108332 12310833 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123108332 12310833 Infective exacerbation of chronic obstructive airways disease
123108332 12310833 Pneumonia

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
123108332 12310833 1 20141009 20141029 0
123108332 12310833 2 20160310 20160317 0
123108332 12310833 3 20160310 0
123108332 12310833 4 20141009 20141030 0
123108332 12310833 5 20160310 20160317 0
123108332 12310833 6 20160318 0