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
125874781 12587478 1 I 20160708 20160713 20160725 20160725 EXP IT-PFIZER INC-2016345472 PFIZER 74.00 YR F Y 0.00000 20160725 MD 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
125874781 12587478 1 PS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 175 MG/M2, CYCLIC Y 76131 175 MG/M**2
125874781 12587478 2 C CARBOPLATIN. CARBOPLATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125874781 12587478 1 Ovarian epithelial cancer

Outcome of event

Event ID CASEID OUTC COD
125874781 12587478 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125874781 12587478 Chest pain
125874781 12587478 Dyspnoea
125874781 12587478 Erythema
125874781 12587478 Throat tightness

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
125874781 12587478 1 20160617 20160708 0