The Safety Rates Drug Report

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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
125799174 12579917 4 F 2016 20160826 20160721 20160903 EXP GB-AMGEN-GBRSP2016084662 AMGEN 63.00 YR A F Y 0.00000 20160903 OT GB GB

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
125799174 12579917 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 UNKNOWN FORMULATION
125799174 12579917 2 SS APREPITANT. APREPITANT 1 Oral UNK 0
125799174 12579917 3 SS ABRAXANE PACLITAXEL 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125799174 12579917 1 Product used for unknown indication
125799174 12579917 2 Product used for unknown indication
125799174 12579917 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125799174 12579917 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125799174 12579917 Back pain
125799174 12579917 Body temperature fluctuation
125799174 12579917 Diarrhoea
125799174 12579917 Fatigue
125799174 12579917 Pain
125799174 12579917 Pain in extremity
125799174 12579917 Pyrexia
125799174 12579917 White blood cell count increased

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

no results found

Therapies reported

no results found