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
125245241 12524524 1 I 20160523 20160704 20160704 PER US-ASTRAZENECA-2016SE56329 ASTRAZENECA 0.00 F Y 49.40000 KG 20160704 CN 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
125245241 12524524 1 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 5.0MG UNKNOWN 0 5 MG
125245241 12524524 2 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 40 MG TABLET QD
125245241 12524524 3 C ASPIRIN. ASPIRIN 1 Oral 0 81 MG QD
125245241 12524524 4 C PREDNISONE. PREDNISONE 1 Oral 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125245241 12524524 1 Cardiac disorder
125245241 12524524 2 Blood cholesterol abnormal
125245241 12524524 3 Cardiac disorder
125245241 12524524 4 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125245241 12524524 Asthenia
125245241 12524524 Decreased appetite
125245241 12524524 Nausea
125245241 12524524 Rheumatoid arthritis
125245241 12524524 Weight decreased

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
125245241 12524524 1 2000 0
125245241 12524524 2 2003 0
125245241 12524524 3 2000 0
125245241 12524524 4 20160509 0