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
120692293 12069229 3 F 201605 20160525 20160211 20160922 PER US-AMGEN-USASP2016015235 AMGEN 75.00 YR E M Y 0.00000 20160922 CN 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
120692293 12069229 1 PS NEUPOGEN FILGRASTIM 1 Unknown UNK, 2 WEEK THERAPY TWICE U 103353 UNKNOWN FORMULATION
120692293 12069229 2 SS NEUPOGEN FILGRASTIM 1 Unknown UNK, 2 WEEK THERAPY TWICE U 103353 UNKNOWN FORMULATION
120692293 12069229 3 C VIDAZA AZACITIDINE 1 UNK 0
120692293 12069229 4 C PREDNISONE. PREDNISONE 1 UNK, FOR 2 WEEKS 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120692293 12069229 1 Product used for unknown indication
120692293 12069229 3 Acute myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
120692293 12069229 HO
120692293 12069229 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120692293 12069229 Neutrophil count abnormal
120692293 12069229 Neutrophil count decreased
120692293 12069229 Platelet count decreased
120692293 12069229 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
120692293 12069229 1 20160126 0
120692293 12069229 2 20160503 0
120692293 12069229 3 20160523 0