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
127340022 12734002 2 F 2016 20160912 20160912 20160920 PER US-CELGENEUS-USA-2016091610 CELGENE 60.00 YR F Y 0.00000 20160920 PH 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
127340022 12734002 1 PS THALOMID THALIDOMIDE 1 Oral U 20785 50 MG CAPSULES QD
127340022 12734002 2 SS THALOMID THALIDOMIDE 1 Oral U 20785 100 MG CAPSULES QD
127340022 12734002 3 SS THALOMID THALIDOMIDE 1 Oral U 20785 100 MG CAPSULES QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127340022 12734002 1 Systemic lupus erythematosus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127340022 12734002 Adverse drug reaction
127340022 12734002 Hypoaesthesia
127340022 12734002 Memory impairment
127340022 12734002 Paraesthesia
127340022 12734002 Somnolence

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
127340022 12734002 1 20160412 0
127340022 12734002 2 201605 0
127340022 12734002 3 201607 20160907 0