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
125767801 12576780 1 I 20150328 20160712 20160720 20160720 EXP CH-SM-2016-05793 CH-SA-2016SA129018 AVENTIS 84.00 YR E F Y 0.00000 20160720 MD CH CH

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
125767801 12576780 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y UNK 20839 75 MG QD
125767801 12576780 2 I MARCOUMAR PHENPROCOUMON 1 Oral Y UNK 0 1 DF TABLET
125767801 12576780 3 I ASPIRIN CARDIO ASPIRIN 1 Oral Y UNK 0 100 MG QD
125767801 12576780 4 C ATORVASTATIN ATORVASTATIN 1 0
125767801 12576780 5 C CIPRALEX ESCITALOPRAM OXALATE 1 0
125767801 12576780 6 C PANTOZOL PANTOPRAZOLE SODIUM 1 0
125767801 12576780 7 C CONCOR BISOPROLOL FUMARATE 1 0
125767801 12576780 8 C ALDACTONE SPIRONOLACTONE 1 0
125767801 12576780 9 C TOREM TORSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125767801 12576780 1 Myocardial infarction
125767801 12576780 2 Atrial flutter
125767801 12576780 3 Myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
125767801 12576780 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125767801 12576780 International normalised ratio increased
125767801 12576780 Lower gastrointestinal 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
125767801 12576780 1 201408 20150328 0
125767801 12576780 2 201407 20150328 0
125767801 12576780 3 201408 20150328 0