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
126295233 12629523 3 F 20160801 20160818 20160808 20160827 EXP JP-AMGEN-JPNSP2016102073 AMGEN 57.00 YR A F Y 0.00000 20160827 PH JP JP

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
126295233 12629523 1 PS G-LASTA PEGFILGRASTIM 1 Subcutaneous UNK U 125031 SOLUTION FOR INJECTION
126295233 12629523 2 SS ADRIACIN DOXORUBICIN HYDROCHLORIDE 1 Intravenous drip 30 MG/M2, UNK 0 30 MG/M**2 INJECTION
126295233 12629523 3 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous drip 2000 MG/M2, UNK 0 2000 MG/M**2 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126295233 12629523 1 Product used for unknown indication
126295233 12629523 2 Product used for unknown indication
126295233 12629523 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126295233 12629523 HO
126295233 12629523 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126295233 12629523 Febrile neutropenia

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
126295233 12629523 1 20160727 20160727 0
126295233 12629523 2 20160721 20160722 0
126295233 12629523 3 20160721 20160725 0