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
112020112 11202011 2 F 20110304 20160720 20150619 20160726 PER US-CELGENEUS-USA-2014113821 CELGENE 71.68 YR Y 0.00000 20160726 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
112020112 11202011 1 PS REVLIMID LENALIDOMIDE 1 Oral N U 21880 25 MG CAPSULES
112020112 11202011 2 SS REVLIMID LENALIDOMIDE 1 Oral N U 21880 CAPSULES
112020112 11202011 3 SS REVLIMID LENALIDOMIDE 1 Oral N U 21880 CAPSULES
112020112 11202011 4 SS REVLIMID LENALIDOMIDE 1 Oral N U 21880 CAPSULES
112020112 11202011 5 SS DECADRON DEXAMETHASONE 1 Oral U U UNKNOWN 0 40 MG UNKNOWN /wk
112020112 11202011 6 SS DECADRON DEXAMETHASONE 1 Oral U U UNKNOWN 0 40 MG UNKNOWN
112020112 11202011 7 SS DECADRON DEXAMETHASONE 1 Oral U U UNKNOWN 0 UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112020112 11202011 1 Plasma cell myeloma
112020112 11202011 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
112020112 11202011 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112020112 11202011 Large granular lymphocytosis
112020112 11202011 Urinary tract infection

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
112020112 11202011 1 20110107 20110204 0
112020112 11202011 2 20110729 20110930 0
112020112 11202011 3 20120214 20120701 0
112020112 11202011 4 20140618 20141111 0
112020112 11202011 5 20110107 20110204 0
112020112 11202011 6 20110309 20110506 0
112020112 11202011 7 20140618 0