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
126169311 12616931 1 I 20101206 20160803 20160803 PER US-ASTRAZENECA-2010SE57984 ASTRAZENECA 67.00 YR M Y 104.30000 KG 20160803 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
126169311 12616931 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 TABLET
126169311 12616931 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 5 MG TABLET QD
126169311 12616931 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126169311 12616931 1 Blood cholesterol increased
126169311 12616931 2 Blood cholesterol increased
126169311 12616931 3 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126169311 12616931 Blood cholesterol abnormal
126169311 12616931 Coronary artery disease
126169311 12616931 Myalgia
126169311 12616931 Wrong patient received medication

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
126169311 12616931 3 201603 0