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
126403634 12640363 4 F 20160802 20160915 20160810 20160923 EXP US-CELGENEUS-USA-2016081226 CELGENE 71.82 YR M Y 0.00000 20160923 MD 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
126403634 12640363 1 PS THALOMID THALIDOMIDE 1 Oral U UNKNOWN 20785 100 MG CAPSULES
126403634 12640363 2 SS THALOMID THALIDOMIDE 1 Oral 150-300 MG U UNKNOWN 20785 CAPSULES QD
126403634 12640363 3 SS THALOMID THALIDOMIDE 1 Oral U UNKNOWN 20785 100 MG CAPSULES
126403634 12640363 4 SS THALOMID THALIDOMIDE 1 Oral U UNKNOWN 20785 100 MG CAPSULES QD
126403634 12640363 5 C COUMADIN WARFARIN SODIUM 1 Oral 0 5 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126403634 12640363 1 Anaemia
126403634 12640363 2 Haemorrhage
126403634 12640363 5 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
126403634 12640363 OT
126403634 12640363 HO
126403634 12640363 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126403634 12640363 Gastrointestinal haemorrhage
126403634 12640363 Haemorrhagic anaemia

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
126403634 12640363 1 201411 0
126403634 12640363 2 201501 0
126403634 12640363 3 201509 0
126403634 12640363 4 20160822 0
126403634 12640363 5 20160702 0