The Safety Rates Drug Report

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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
118577993 11857799 3 F 20130103 20160804 20151222 20160810 PER US-CELGENEUS-163-21880-13103751 CELGENE 80.95 YR M Y 72.50000 KG 20160810 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
118577993 11857799 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES
118577993 11857799 2 SS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES QOD
118577993 11857799 3 SS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES QOD
118577993 11857799 4 SS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES QOD
118577993 11857799 5 SS DECADRON DEXAMETHASONE 1 Oral U U 0 40 MG UNKNOWN /wk
118577993 11857799 6 SS DECADRON DEXAMETHASONE 1 Oral U U 0 40 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118577993 11857799 1 Plasma cell myeloma
118577993 11857799 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
118577993 11857799 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118577993 11857799 Pneumonia
118577993 11857799 Thrombocytopenia

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
118577993 11857799 1 20110705 20110726 0
118577993 11857799 2 20110908 20120301 0
118577993 11857799 3 20120401 20130103 0
118577993 11857799 4 20130124 20130302 0
118577993 11857799 5 20110705 0
118577993 11857799 6 20121005 20130530 0