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
123539143 12353914 3 F 20160419 20160902 20160511 20160907 EXP US-ROCHE-1753514 ROCHE 64.00 YR F Y 0.00000 20160907 MD 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
123539143 12353914 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAY 1-14 OF 21-DAY CYCLE?DATE OF LAST DOSE PRIOR TO AE ONSET: 18/APR/2016 20896 TABLET BID
123539143 12353914 2 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) ON DAY 1 OF 21-DAY CYCLE?MOST RECENT DOSE PRIOR TO EVENT ONSET: 04/APR/2016 0 80 MG/M**2
123539143 12353914 3 C PIPERACILLIN SODIUM PIPERACILLIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123539143 12353914 1 Adenocarcinoma gastric
123539143 12353914 2 Adenocarcinoma gastric

Outcome of event

Event ID CASEID OUTC COD
123539143 12353914 HO
123539143 12353914 DE
123539143 12353914 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123539143 12353914 Febrile neutropenia
123539143 12353914 Respiratory failure
123539143 12353914 Septic shock

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
123539143 12353914 1 20160404 20160419 0
123539143 12353914 2 20160404 0