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
125808941 12580894 1 I 201606 20160713 20160721 20160721 EXP DK-ASTRAZENECA-2016SE75802 ASTRAZENECA 86.00 YR M Y 0.00000 20160721 MD DK DK

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
125808941 12580894 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 19962 12.5 MG MODIFIED-RELEASE TABLET BID
125808941 12580894 2 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 19962 25 MG MODIFIED-RELEASE TABLET BID
125808941 12580894 3 C CARDOPAX RETARD 2 0
125808941 12580894 4 C CLOPIDOGREL CLOPIDOGREL BISULFATE 1 0
125808941 12580894 5 C GLYCERYL TRINITRATE NITROGLYCERIN 1 0
125808941 12580894 6 C SIMVASTATIN. SIMVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125808941 12580894 1 Cardiac failure congestive
125808941 12580894 2 Cardiac failure congestive
125808941 12580894 3 Cardiac failure congestive
125808941 12580894 4 Myocardial ischaemia
125808941 12580894 5 Angina pectoris
125808941 12580894 6 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
125808941 12580894 OT
125808941 12580894 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125808941 12580894 Chest pain
125808941 12580894 Dizziness
125808941 12580894 Presyncope
125808941 12580894 Ventricular arrhythmia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found