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
77095802 7709580 2 F 20160513 20160513 20101214 20160721 PER US-ASTRAZENECA-2010SE35918 ASTRAZENECA 28222.00 DY F Y 63.50000 KG 20160722 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
77095802 7709580 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD
77095802 7709580 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
77095802 7709580 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77095802 7709580 1 Blood cholesterol abnormal
77095802 7709580 2 Blood cholesterol abnormal
77095802 7709580 3 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
77095802 7709580 Cardiolipin antibody positive
77095802 7709580 Drug dose omission
77095802 7709580 Hot flush
77095802 7709580 Intentional product misuse
77095802 7709580 Myalgia
77095802 7709580 Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found