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
125182712 12518271 2 F 20160203 20160802 20160630 20160811 EXP IT-MINISAL02-347620 IT-PFIZER INC-3174284 PFIZER 54.00 YR F Y 0.00000 20160811 PH 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
125182712 12518271 1 PS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 45 MG, CYCLIC N UNK 22234 45 MG SOLUTION FOR INJECTION
125182712 12518271 2 SS OXALIPLATIN. OXALIPLATIN 1 Intravenous (not otherwise specified) 105 MG, CYCLIC N UNK 78813 105 MG SOLUTION FOR INJECTION
125182712 12518271 3 SS CAPECITABINE. CAPECITABINE 1 Oral 2100 MG, CYCLIC N UNK 0 2100 MG TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125182712 12518271 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125182712 12518271 Diarrhoea
125182712 12518271 Pain
125182712 12518271 Palmar-plantar erythrodysaesthesia syndrome
125182712 12518271 Peripheral swelling
125182712 12518271 Skin exfoliation

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
125182712 12518271 1 20160125 20160215 0
125182712 12518271 2 20160125 20160215 0
125182712 12518271 3 20160125 20160215 0