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
122609992 12260999 2 F 20160125 20160713 20160412 20160719 PER US-CELGENEUS-USA-2016041709 CELGENE 62.05 YR F Y 69.40000 KG 20160719 OT 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
122609992 12260999 1 PS POMALYST POMALIDOMIDE 1 Oral 2 MILLIGRAM U UNKNOWN 204026 2 MG CAPSULES
122609992 12260999 2 SS CYTOXAN CYCLOPHOSPHAMIDE 1 Intravenous drip U UNKNOWN 204026 600 MG/M**2 INJECTION
122609992 12260999 3 SS PREDNISONE. PREDNISONE 1 Oral 600 MILLIGRAM/SQ. METER U UNKNOWN 204026 50 MG UNKNOWN QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122609992 12260999 1 Plasma cell myeloma
122609992 12260999 2 Plasma cell myeloma
122609992 12260999 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
122609992 12260999 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122609992 12260999 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
122609992 12260999 1 20150217 20151204 0
122609992 12260999 2 20150217 20151204 0
122609992 12260999 3 20150217 20151204 0