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
124322532 12432253 2 F 20160518 20160913 20160603 20160919 PER US-CELGENEUS-USA-2016056836 CELGENE 53.48 YR F Y 68.10000 KG 20160919 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
124322532 12432253 1 PS REVLIMID LENALIDOMIDE 1 Oral U A2058C 21880 10 MG CAPSULES QD
124322532 12432253 2 SS REVLIMID LENALIDOMIDE 1 Oral U A2058C 21880 10 MG CAPSULES
124322532 12432253 3 SS AMOXICILLIN. AMOXICILLIN 1 Unknown D U 0 UNKNOWN
124322532 12432253 4 C AMBIEN ZOLPIDEM TARTRATE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124322532 12432253 1 Myelodysplastic syndrome
124322532 12432253 3 Swelling face
124322532 12432253 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124322532 12432253 DS
124322532 12432253 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124322532 12432253 Drug hypersensitivity
124322532 12432253 Haemoglobin decreased
124322532 12432253 Tooth 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
124322532 12432253 1 201308 0
124322532 12432253 2 20160422 0
124322532 12432253 3 201605 0