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
124633173 12463317 3 F 20160624 20160614 20160708 EXP JP-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-118427 RANBAXY 74.00 YR M Y 0.00000 20160708 OT GB JP

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
124633173 12463317 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown U 90494
124633173 12463317 2 I PACLITAXEL. PACLITAXEL 1 Unknown 21 DAILY; THE DOSE WAS 94.9 MG PER WEEK U 0 200 MG/M**2
124633173 12463317 3 C CARBOPLATIN. CARBOPLATIN 1 Unknown 21 DAILY U 0 200 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124633173 12463317 1 Myocardial infarction
124633173 12463317 2 Lung adenocarcinoma recurrent
124633173 12463317 3 Lung adenocarcinoma recurrent

Outcome of event

Event ID CASEID OUTC COD
124633173 12463317 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124633173 12463317 Drug interaction
124633173 12463317 Febrile neutropenia
124633173 12463317 Leukopenia
124633173 12463317 Neutropenia

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

no results found

Therapies reported

no results found