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
125903981 12590398 1 I 20120204 20160720 20160725 20160725 PER US-CELGENEUS-USA-2016075375 CELGENE 56.93 YR Y 0.00000 20160725 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
125903981 12590398 1 PS REVLIMID LENALIDOMIDE 1 Oral U U 21880 25 MG CAPSULES
125903981 12590398 2 SS REVLIMID LENALIDOMIDE 1 Oral U U 21880 10 MG CAPSULES
125903981 12590398 3 SS REVLIMID LENALIDOMIDE 1 Oral U U 21880 10 MG CAPSULES
125903981 12590398 4 SS REVLIMID LENALIDOMIDE 1 Oral U U 21880 5 MG CAPSULES
125903981 12590398 5 SS REVLIMID LENALIDOMIDE 1 Oral U U 21880 5 MG CAPSULES
125903981 12590398 6 SS ALKERAN MELPHALAN 1 Intravenous drip U U 0 200 UG/M**2 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125903981 12590398 1 Plasma cell myeloma
125903981 12590398 6 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125903981 12590398 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125903981 12590398 Febrile 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
125903981 12590398 1 20110510 20110812 0
125903981 12590398 2 20120418 20120806 0
125903981 12590398 3 20120830 20121203 0
125903981 12590398 4 20121219 20140301 0
125903981 12590398 5 20140310 20140925 0
125903981 12590398 6 20120124 20120124 0