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
127524621 12752462 1 I 20160907 20160916 20160916 EXP US-ROCHE-1830190 ROCHE 0.00 F Y 60.77000 KG 20160916 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
127524621 12752462 1 PS NEUPOGEN FILGRASTIM 1 Unknown 300 MUG, DAILY 103353 300 UG QD
127524621 12752462 2 SS ROCEPHIN CEFTRIAXONE SODIUM 1 Unknown U 63239
127524621 12752462 3 SS CEFEPIME CEFEPIME HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0
127524621 12752462 4 C CYTOXAN CYCLOPHOSPHAMIDE 1 Unknown 0
127524621 12752462 5 C TAXOTERE DOCETAXEL 1 0
127524621 12752462 6 C ADRIAMYCIN DOXORUBICIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127524621 12752462 1 Neutropenia
127524621 12752462 2 Pyrexia
127524621 12752462 3 Pyrexia
127524621 12752462 6 Drug hypersensitivity

Outcome of event

Event ID CASEID OUTC COD
127524621 12752462 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127524621 12752462 Blood count abnormal
127524621 12752462 Bone pain
127524621 12752462 Clostridium difficile infection
127524621 12752462 Febrile neutropenia
127524621 12752462 Neutrophil count increased
127524621 12752462 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
127524621 12752462 1 2016 0
127524621 12752462 2 2016 0
127524621 12752462 3 2016 0
127524621 12752462 4 20160609 0