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
124835903 12483590 3 F 20160616 20160722 20160621 20160725 EXP IT-ROCHE-1779223 ROCHE 57.15 YR F Y 88.00000 KG 20160725 OT IT IT

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
124835903 12483590 1 PS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) Y N1026H02 103792 700 MG SOLUTION FOR INFUSION /cycle
124835903 12483590 2 C VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Unknown 0 35 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124835903 12483590 1 Breast cancer
124835903 12483590 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
124835903 12483590 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124835903 12483590 Myalgia
124835903 12483590 Pulse absent
124835903 12483590 Skin discolouration
124835903 12483590 Tremor
124835903 12483590 Unresponsive to stimuli

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
124835903 12483590 1 20160616 20160616 0
124835903 12483590 2 20160616 20160616 0