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
126602952 12660295 2 F 201309 20160815 20160817 20160825 EXP US-CELGENEUS-USA-2016084080 CELGENE 68.28 YR M Y 0.00000 20160825 CN 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
126602952 12660295 1 PS THALOMID THALIDOMIDE 1 Oral U U UNKNOWN 20785 100 MG CAPSULES QD
126602952 12660295 2 SS THALOMID THALIDOMIDE 1 Oral 200-100 MG U U UNKNOWN 20785 CAPSULES QD
126602952 12660295 3 SS THALOMID THALIDOMIDE 1 Oral U U UNKNOWN 20785 100 MG CAPSULES QD
126602952 12660295 4 SS THALOMID THALIDOMIDE 1 Oral U U UNKNOWN 20785 200 MG CAPSULES QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126602952 12660295 1 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126602952 12660295 OT
126602952 12660295 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126602952 12660295 Cystitis
126602952 12660295 Femur fracture
126602952 12660295 Pain
126602952 12660295 Sepsis
126602952 12660295 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
126602952 12660295 1 200608 0
126602952 12660295 2 200701 0
126602952 12660295 3 201401 0
126602952 12660295 4 201603 0