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
125637941 12563794 1 I 2016 20160712 20160716 20160716 EXP US-AMGEN-USASP2016090673 AMGEN 47.00 YR A F Y 0.00000 20160716 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
125637941 12563794 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U A40228-0006628 125031 SOLUTION FOR INJECTION
125637941 12563794 2 SS NEUPOGEN FILGRASTIM 1 Unknown 480 MG, QD (ONCE A DAY FOR 3 DAYS) U 0 480 MG UNKNOWN FORMULATION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125637941 12563794 1 Product used for unknown indication
125637941 12563794 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125637941 12563794 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125637941 12563794 Drug dose omission
125637941 12563794 Neutrophil count abnormal
125637941 12563794 White blood cell count 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
125637941 12563794 2 20160623 20160627 0