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
121422892 12142289 2 F 201508 20160727 20160303 20160802 PER US-CELGENEUS-USA-2016030161 CELGENE 88.16 YR F Y 0.00000 20160802 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
121422892 12142289 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U 21880 10 MG CAPSULES QD
121422892 12142289 2 SS REVLIMID LENALIDOMIDE 1 Oral 1 MILLIGRAM/SQ. METER Y U 21880 10 MG CAPSULES QOD
121422892 12142289 3 SS REVLIMID LENALIDOMIDE 1 Oral Y U 21880 5 MG CAPSULES QOD
121422892 12142289 4 SS VELCADE BORTEZOMIB 1 Unknown U U 0 1 MG/M**2 UNKNOWN
121422892 12142289 5 C ZOMETA ZOLEDRONIC ACID 1 Intravenous drip 3 MILLIGRAM 0 3 MG UNKNOWN /month
121422892 12142289 6 C DECADRON DEXAMETHASONE 1 Unknown 20 MILLIGRAM 0 20 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121422892 12142289 1 Plasma cell myeloma
121422892 12142289 4 Product used for unknown indication
121422892 12142289 5 Product used for unknown indication
121422892 12142289 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121422892 12142289 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121422892 12142289 Haemoglobin decreased
121422892 12142289 Neutropenia

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
121422892 12142289 1 201507 0
121422892 12142289 2 201508 201510 0
121422892 12142289 3 201510 0
121422892 12142289 4 201603 0
121422892 12142289 5 201508 201512 0
121422892 12142289 6 201507 0