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
98117465 9811746 5 F 201106 20160627 20140110 20160705 EXP US-SANOFI-AVENTIS-2013SA055834 AVENTIS 78.00 YR E F Y 0.00000 20160705 MD US US

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
98117465 9811746 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNKNOWN 20839 1 DF TABLET QD
98117465 9811746 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNKNOWN 20839 1 DF TABLET QD
98117465 9811746 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNKNOWN 20839 1 DF TABLET QD
98117465 9811746 4 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98117465 9811746 1 Acute coronary syndrome
98117465 9811746 2 Stent placement
98117465 9811746 3 Peripheral arterial occlusive disease

Outcome of event

Event ID CASEID OUTC COD
98117465 9811746 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98117465 9811746 Blood disorder
98117465 9811746 Gastrointestinal haemorrhage
98117465 9811746 Multiple injuries
98117465 9811746 Ulcer haemorrhage

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
98117465 9811746 1 20020101 20110613 0
98117465 9811746 2 20020101 20110613 0
98117465 9811746 3 20020101 20110613 0