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
125438911 12543891 1 I 201604 20160706 20160711 20160711 EXP GB-AMGEN-GBRSP2016088397 AMGEN 45.00 YR A F Y 0.00000 20160711 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
125438911 12543891 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 UNKNOWN FORMULATION
125438911 12543891 2 SS TAXOTERE DOCETAXEL 1 Intravenous (not otherwise specified) UNK UNK, 1/3 WEEKS 0 Q3W
125438911 12543891 3 SS ETHANOL ALCOHOL 1 Unknown UNK 0
125438911 12543891 4 C PEGFILGRASTIM PEGFILGRASTIM 1 Subcutaneous UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125438911 12543891 1 Product used for unknown indication
125438911 12543891 2 Breast cancer
125438911 12543891 3 Product used for unknown indication
125438911 12543891 4 White blood cell count decreased

Outcome of event

Event ID CASEID OUTC COD
125438911 12543891 OT
125438911 12543891 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125438911 12543891 Alopecia
125438911 12543891 Dyspnoea
125438911 12543891 Fatigue
125438911 12543891 Lower respiratory tract infection
125438911 12543891 Micturition disorder

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
125438911 12543891 2 20160324 20160324 0
125438911 12543891 4 20160324 0