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
125471483 12547148 3 F 20160706 20160711 20160714 EXP US-ASTRAZENECA-2016SE73971 ASTRAZENECA 0.00 F Y 122.50000 KG 20160714 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
125471483 12547148 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U U 21366 5 MG TABLET QD
125471483 12547148 2 SS BRILINTA TICAGRELOR 1 Oral 900 MG U 0 90 MG TABLET Q12H
125471483 12547148 3 SS BRILINTA TICAGRELOR 1 Oral 900 MG U 0 90 MG TABLET Q12H
125471483 12547148 4 C ASPIRIN. ASPIRIN 1 Oral 0 81 MG QD
125471483 12547148 5 C PLAVIX CLOPIDOGREL BISULFATE 1 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125471483 12547148 1 Blood cholesterol increased
125471483 12547148 2 Acute coronary syndrome
125471483 12547148 3 Anticoagulant therapy
125471483 12547148 4 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
125471483 12547148 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125471483 12547148 Dyspnoea
125471483 12547148 Off label use
125471483 12547148 Product use issue

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
125471483 12547148 1 201511 0
125471483 12547148 2 20160519 20160523 0
125471483 12547148 3 20160519 20160523 0
125471483 12547148 4 20160519 0
125471483 12547148 5 20160524 0