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
126794371 12679437 1 I 2013 20160816 20160824 20160824 EXP FR-ASTRAZENECA-2016SE89571 ASTRAZENECA 93.00 YR M Y 0.00000 20160824 MD 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
126794371 12679437 1 PS MOPRAL OMEPRAZOLE SODIUM 1 Oral Y U 19810 20 MG QD
126794371 12679437 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y U 0 75 MG QD
126794371 12679437 3 C FUMAFER FERROUS FUMARATE 1 Oral 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126794371 12679437 1 Gastrointestinal haemorrhage
126794371 12679437 2 Myocardial infarction
126794371 12679437 3 Anaemia

Outcome of event

Event ID CASEID OUTC COD
126794371 12679437 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126794371 12679437 Abdominal pain
126794371 12679437 Asthenia
126794371 12679437 Cognitive disorder
126794371 12679437 Confusional state
126794371 12679437 Constipation
126794371 12679437 Depressed level of consciousness
126794371 12679437 Depression
126794371 12679437 Fall
126794371 12679437 Fatigue
126794371 12679437 Gastric haemorrhage
126794371 12679437 General physical health deterioration
126794371 12679437 Muscular weakness
126794371 12679437 Myalgia
126794371 12679437 Pain
126794371 12679437 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
126794371 12679437 1 2016 0