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
125245931 12524593 1 I 20160329 20160626 20160704 20160704 EXP IL-ASTRAZENECA-2016SE70964 ASTRAZENECA 62.00 YR M Y 0.00000 20160704 IL IL

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
125245931 12524593 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 TABLET
125245931 12524593 2 C VECTOR 2 0 160 MG
125245931 12524593 3 C CARDILOC BISOPROLOL FUMARATE 1 0 2.5 MG QD
125245931 12524593 4 C TRITACE RAMIPRIL 1 0 5 MG QD
125245931 12524593 5 C PLAVIX CLOPIDOGREL BISULFATE 1 0 75 MG QD
125245931 12524593 6 C ASPIRIN. ASPIRIN 1 0 100 MG QD
125245931 12524593 7 C LOSEC OMEPRAZOLE 1 0 20 MG QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125245931 12524593 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125245931 12524593 Asthenia
125245931 12524593 Dizziness
125245931 12524593 Dyspnoea
125245931 12524593 Hemiparesis
125245931 12524593 Lip swelling
125245931 12524593 Swelling face

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
125245931 12524593 1 20160329 0