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
124758983 12475898 3 F 20160601 20160701 20160617 20160713 EXP IT-MINISAL02-362092 IT-TEVA-668061ACC TEVA 71.17 YR F Y 0.00000 20160714 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
124758983 12475898 1 PS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 175 MG/M2 CYCLICAL Y U 75297 175 MG/M**2
124758983 12475898 2 C CARBOPLATIN. CARBOPLATIN 1 U 0
124758983 12475898 3 C BEVACIZUMAB BEVACIZUMAB 1 7.5 MG/KG U 0 7.5 MG/KG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124758983 12475898 1 Non-small cell lung cancer recurrent
124758983 12475898 2 Product used for unknown indication
124758983 12475898 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124758983 12475898 HO
124758983 12475898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124758983 12475898 Disorganised speech
124758983 12475898 Dyspnoea
124758983 12475898 Erythema

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
124758983 12475898 1 20160217 20160601 0