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
981007013 9810070 13 F 2009 20160906 20140110 20160915 EXP US-SANOFI-AVENTIS-2013SA071481 AVENTIS 56.00 YR A M Y 74.10000 KG 20160915 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
981007013 9810070 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U UNKNOWN 20839 75 MG TABLET QD
981007013 9810070 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U UNK 20839 600 MG TABLET 1X
981007013 9810070 3 SS ASPIRIN. ASPIRIN 1 Unknown U UNKNOWN 0
981007013 9810070 4 C LIPITOR ATORVASTATIN CALCIUM 1 0 20 MG QD
981007013 9810070 5 C NITROGLYCERINE NITROGLYCERIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
981007013 9810070 1 Prophylaxis
981007013 9810070 2 Prophylaxis
981007013 9810070 4 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
981007013 9810070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
981007013 9810070 Aneurysm
981007013 9810070 Cerebral haemorrhage
981007013 9810070 Cerebrovascular accident
981007013 9810070 Haemorrhage intracranial
981007013 9810070 Hemiparesis
981007013 9810070 Seizure
981007013 9810070 Sensory disturbance

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
981007013 9810070 1 2008 20090102 0
981007013 9810070 2 20031223 20031223 0
981007013 9810070 3 2008 0