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
124709322 12470932 2 F 20160601 20160607 20160616 20160714 EXP PHHY2016IT080114 SANDOZ 75.73 YR M Y 0.00000 20160714 OT 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
124709322 12470932 1 PS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) 450 MG, CYCLIC U 76959 450 MG SOLUTION FOR INFUSION
124709322 12470932 2 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1500 MG, CYCLIC 0 1500 MG POWDER FOR SOL FOR INF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124709322 12470932 1 Lung neoplasm malignant
124709322 12470932 2 Lung neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
124709322 12470932 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124709322 12470932 Dysarthria
124709322 12470932 Dyspnoea
124709322 12470932 Hyperhidrosis
124709322 12470932 Loss of consciousness

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found