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
123725472 12372547 2 F 20160809 20160516 20160817 EXP US-ASTRAZENECA-2016SE48894 ASTRAZENECA 0.00 M Y 100.70000 KG 20160818 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
123725472 12372547 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 40 MG TABLET QD
123725472 12372547 2 SS BRILINTA TICAGRELOR 1 Oral 22433 90 MG TABLET BID
123725472 12372547 3 SS BRILINTA TICAGRELOR 1 Oral 22433 90 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123725472 12372547 1 Blood cholesterol
123725472 12372547 2 Acute coronary syndrome
123725472 12372547 3 Stent placement

Outcome of event

Event ID CASEID OUTC COD
123725472 12372547 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123725472 12372547 Dyspnoea
123725472 12372547 Myocardial infarction
123725472 12372547 Therapeutic response unexpected

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
123725472 12372547 2 20160417 0
123725472 12372547 3 20160417 0