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
104412613 10441261 3 F 20131018 20160909 20140909 20160923 EXP GB-CELGENEUS-167-20785-13110284 CELGENE 70.00 YR M Y 0.00000 20160923 MD GB GB

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
104412613 10441261 1 PS THALIDOMIDE THALIDOMIDE 1 Oral 50 MILLIGRAM U 20785 50 MG CAPSULES QD
104412613 10441261 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral U 0 500 MG TABLETS
104412613 10441261 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral U 0 300 MG TABLETS
104412613 10441261 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 0 20 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104412613 10441261 1 Plasma cell myeloma
104412613 10441261 2 Plasma cell myeloma
104412613 10441261 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
104412613 10441261 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104412613 10441261 Fall
104412613 10441261 Muscle atrophy
104412613 10441261 Muscular weakness
104412613 10441261 Nausea
104412613 10441261 Pneumonia aspiration
104412613 10441261 Vomiting

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
104412613 10441261 1 20130807 0
104412613 10441261 2 20130807 20131016 0
104412613 10441261 4 20130807 0