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
126858551 12685855 1 I 2013 20160816 20160825 20160825 EXP FR-SA-2016SA151307 AVENTIS 93.00 YR E M Y 0.00000 20160825 OT FR FR

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
126858551 12685855 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y U 20839 1 DF FILM-COATED TABLET QD
126858551 12685855 2 SS MOPRAL OMEPRAZOLE SODIUM 1 Oral 20 MG GASTRO-RESISTANT TABLET Y U 0 1 DF QD
126858551 12685855 3 C FUMAFER FERROUS FUMARATE 1 Oral 0 66 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126858551 12685855 1 Myocardial infarction
126858551 12685855 2 Gastrointestinal haemorrhage
126858551 12685855 3 Anaemia

Outcome of event

Event ID CASEID OUTC COD
126858551 12685855 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126858551 12685855 Asthenia
126858551 12685855 Confusional state
126858551 12685855 Depressed level of consciousness
126858551 12685855 Depression
126858551 12685855 Fall
126858551 12685855 Fatigue
126858551 12685855 Gastric haemorrhage
126858551 12685855 Muscular weakness
126858551 12685855 Myalgia
126858551 12685855 Vertigo

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
126858551 12685855 2 2016 0