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
100067962 10006796 2 F 20140318 20140311 20140331 EXP AUR-APL-2014-02647 AUROBINDO 74.00 YR F N 0.00000 20140328 N OT GB

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
100067962 10006796 1 PS CLOPIDOGREL (CLOPIDOGREL) 1 U 50540
100067962 10006796 2 SS GINKGO BILOBA (GINKGO BILOBA) 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100067962 10006796 1 Antiplatelet therapy
100067962 10006796 2 Menopausal symptoms

Outcome of event

Event ID CASEID OUTC COD
100067962 10006796 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100067962 10006796 Chromaturia
100067962 10006796 Contusion
100067962 10006796 Dizziness
100067962 10006796 Drug interaction
100067962 10006796 Feeling abnormal
100067962 10006796 Haematuria
100067962 10006796 Self-medication
100067962 10006796 Vaginal haemorrhage

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

Event ID CASEID RPSR COD
100067962 10006796 LIT
100067962 10006796 FGN
100067962 10006796 HP

Therapies reported

no results found