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
118827802 11882780 2 F 20131219 20160801 20151231 20160808 PER US-CELGENEUS-163-21880-13125166 CELGENE 65.02 YR F Y 118.60000 KG 20160808 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
118827802 11882780 1 PS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 25 MG CAPSULES
118827802 11882780 2 SS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 15 MG CAPSULES
118827802 11882780 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U U UNKNOWN 0 8 MG TABLETS /wk
118827802 11882780 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U U UNKNOWN 0 8 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118827802 11882780 1 Plasma cell myeloma
118827802 11882780 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
118827802 11882780 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118827802 11882780 Abdominal pain
118827802 11882780 Diarrhoea
118827802 11882780 Pulmonary embolism

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
118827802 11882780 1 20101001 20111012 0
118827802 11882780 2 20111205 0
118827802 11882780 3 20111205 0
118827802 11882780 4 20120913 0