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
118387922 11838792 2 F 20151202 20160720 20151215 20160805 PER US-CELGENEUS-USA-2015122281 CELGENE 86.16 YR M Y 0.00000 20160805 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
118387922 11838792 1 PS REVLIMID LENALIDOMIDE 1 Oral U A0560A 21880 10 MG CAPSULES
118387922 11838792 2 SS REVLIMID LENALIDOMIDE 1 Oral 40 MILLIGRAM U A0560A 21880 10 MG CAPSULES
118387922 11838792 3 SS REVLIMID LENALIDOMIDE 1 Oral U A0560A 21880 5 MG CAPSULES QD
118387922 11838792 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U U 0 40 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118387922 11838792 1 Plasma cell myeloma
118387922 11838792 4 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118387922 11838792 Flushing
118387922 11838792 Neutropenia
118387922 11838792 White blood cell count decreased

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
118387922 11838792 1 201510 20151202 0
118387922 11838792 2 20151204 20160107 0
118387922 11838792 3 20160111 0
118387922 11838792 4 201510 0