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
98116853 9811685 3 F 201105 20160803 20140110 20160812 EXP US-SANOFI-AVENTIS-2013SA045077 AVENTIS 0.00 A F Y 0.00000 20160812 CN 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
98116853 9811685 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNKNOWN 20839 75 MG TABLET QD
98116853 9811685 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNKNOWN 20839 75 MG TABLET QD
98116853 9811685 3 C BETA BLOCKING AGENTS UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98116853 9811685 1 Transient ischaemic attack
98116853 9811685 2 Acute coronary syndrome

Outcome of event

Event ID CASEID OUTC COD
98116853 9811685 OT
98116853 9811685 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
98116853 9811685 Cerebral haemorrhage
98116853 9811685 Death
98116853 9811685 Gastrointestinal haemorrhage
98116853 9811685 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
98116853 9811685 1 2005 201110 0
98116853 9811685 2 2005 201110 0