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
126716201 12671620 1 I 20130823 20130830 20160822 20160822 EXP GB-CELGENEUS-167-20785-13090046 CELGENE 66.00 YR F Y 0.00000 20160822 OT 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
126716201 12671620 1 PS THALOMID THALIDOMIDE 1 Oral 100 MILLIGRAM N U 20785 100 MG CAPSULES QD
126716201 12671620 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral N U 0 500 MG TABLETS QD
126716201 12671620 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral N U 0 40 MG TABLETS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126716201 12671620 1 Plasma cell myeloma
126716201 12671620 2 Plasma cell myeloma
126716201 12671620 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126716201 12671620 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126716201 12671620 Constipation
126716201 12671620 Pain
126716201 12671620 Viral labyrinthitis

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
126716201 12671620 1 20130706 20130821 0
126716201 12671620 2 20130706 20130815 0
126716201 12671620 3 20130706 20130815 0