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
125613631 12561363 1 I 20160628 20160708 20160715 20160715 PER US-CELGENEUS-USA-2016072151 CELGENE 65.74 YR F Y 0.00000 20160715 OT 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
125613631 12561363 1 PS THALOMID THALIDOMIDE 1 Oral N U M9941101-08 20785 150 MG CAPSULES
125613631 12561363 2 SS THALOMID THALIDOMIDE 1 Oral N U M9941101-08 20785 150 MG CAPSULES

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125613631 12561363 1 Hereditary haemorrhagic telangiectasia

Outcome of event

Event ID CASEID OUTC COD
125613631 12561363 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125613631 12561363 Constipation
125613631 12561363 Decreased appetite
125613631 12561363 Fatigue
125613631 12561363 Full blood count decreased
125613631 12561363 Weight decreased

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
125613631 12561363 1 201605 0
125613631 12561363 2 20160617 20160628 0