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
125955381 12595538 1 I 20160708 20160714 20160726 20160726 EXP IT-MINISAL02-367201 IT-TEVA-678724ACC TEVA 74.52 YR F Y 0.00000 20160726 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
125955381 12595538 1 PS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 175 MG/M2 CYCLICAL Y 75297 175 MG/M**2
125955381 12595538 2 C CARBOPLATIN. CARBOPLATIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125955381 12595538 1 Ovarian epithelial cancer
125955381 12595538 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125955381 12595538 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125955381 12595538 Chest pain
125955381 12595538 Dyspnoea
125955381 12595538 Flushing
125955381 12595538 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
125955381 12595538 1 20160617 20160708 0