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
125054852 12505485 2 F 2016 20160628 20160628 20160707 PER US-CELGENEUS-USA-2016064912 CELGENE 0.00 F Y 79.45000 KG 20160707 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
125054852 12505485 1 PS THALOMID THALIDOMIDE 1 Oral U B2005AB 20785 50 MG CAPSULES QD
125054852 12505485 2 SS THALOMID THALIDOMIDE 1 Oral U B2005AB 20785 100 MG CAPSULES QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125054852 12505485 1 Gastric haemorrhage

Outcome of event

Event ID CASEID OUTC COD
125054852 12505485 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125054852 12505485 Fatigue
125054852 12505485 Muscular weakness
125054852 12505485 Neuropathy peripheral
125054852 12505485 Tremor

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
125054852 12505485 1 20160421 0
125054852 12505485 2 201605 0