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
90600511 9060051 1 I 20130125 0 20130207 20130207 DIR 6.00 YR M N 24.30000 KG 20130131 MD 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
90600511 9060051 1 PS VORINOSTAT 1 ORAL D D G011864 0 200 MG QD
90600511 9060051 2 SS I-MIBG 1 INTRAVENOUS D 0 437 MCI 1X
90600511 9060051 4 C NEUPOGEN 1 0
90600511 9060051 5 C POTASSIUM IODIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90600511 9060051 1 Neuroblastoma
90600511 9060051 2 Neuroblastoma

Outcome of event

Event ID CASEID OUTC COD
90600511 9060051 HO
90600511 9060051 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90600511 9060051 Blood blister
90600511 9060051 Contusion
90600511 9060051 Haemorrhage
90600511 9060051 Petechiae
90600511 9060051 Thrombocytopenia
90600511 9060051 Tongue haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
90600511 9060051 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
90600511 9060051 1 20121203 20121217 0
90600511 9060051 2 20121205 0