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
124056042 12405604 2 F 201602 20160829 20160526 20160830 EXP CO-ROCHE-1762556 ROCHE 49.49 YR F Y 40.00000 KG 20160830 CN CO CO

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
124056042 12405604 1 PS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) U 103792 380 MG SOLUTION FOR INFUSION
124056042 12405604 2 SS CAPECITABINE. CAPECITABINE 1 Oral U 20896 2000 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124056042 12405604 1 Breast cancer
124056042 12405604 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
124056042 12405604 HO
124056042 12405604 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124056042 12405604 Diarrhoea
124056042 12405604 Joint injury
124056042 12405604 Limb injury
124056042 12405604 Weight decreased
124056042 12405604 Xeroderma

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
124056042 12405604 1 20150313 0
124056042 12405604 2 20150313 0