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
127410261 12741026 1 I 2016 20160907 20160914 20160914 EXP US-AMGEN-USASP2016121028 AMGEN 0.00 F Y 60.77000 KG 20160914 OT 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
127410261 12741026 1 PS NEUPOGEN FILGRASTIM 1 Unknown 300 MUG, QD (300 MCG, DAILY) 103353 300 UG UNKNOWN FORMULATION QD
127410261 12741026 2 SS ROCEPHIN CEFTRIAXONE SODIUM 1 Unknown UNK 0
127410261 12741026 3 SS CEFEPIME CEFEPIME HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK 0
127410261 12741026 4 C CYTOXAN CYCLOPHOSPHAMIDE 1 UNK 0
127410261 12741026 5 C TAXOTERE DOCETAXEL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127410261 12741026 1 Neutropenia
127410261 12741026 2 Pyrexia
127410261 12741026 3 Pyrexia

Outcome of event

Event ID CASEID OUTC COD
127410261 12741026 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127410261 12741026 Blood count abnormal
127410261 12741026 Bone pain
127410261 12741026 Clostridium difficile infection
127410261 12741026 Febrile neutropenia
127410261 12741026 Neutrophil count increased
127410261 12741026 White blood cell 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
127410261 12741026 1 2016 0
127410261 12741026 2 2016 0
127410261 12741026 3 2016 0
127410261 12741026 4 20160609 0
127410261 12741026 5 2016 0