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
124633143 12463314 3 F 20160624 20160614 20160708 EXP JP-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-118424 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
124633143 12463314 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown UNK U U 90494
124633143 12463314 2 I PACLITAXEL. PACLITAXEL 1 Unknown WEEKLY, 6 COURSES, THE DOSE WAS 70.0MG PER WEEK U U 0 40 MG/M**2
124633143 12463314 3 C CARBOPLATIN. CARBOPLATIN 1 Unknown WEEKLY, 6 COURSES U U 0 40 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124633143 12463314 1 Myocardial infarction
124633143 12463314 2 Lung adenocarcinoma stage III
124633143 12463314 3 Lung adenocarcinoma stage III

Outcome of event

Event ID CASEID OUTC COD
124633143 12463314 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124633143 12463314 Drug interaction
124633143 12463314 Febrile neutropenia
124633143 12463314 Leukopenia
124633143 12463314 Neutropenia

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

no results found

Therapies reported

no results found