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
126055131 12605513 1 I 2011 20160616 20160729 20160729 PER US-ASTRAZENECA-2016SE67418 ASTRAZENECA 61.00 YR F Y 63.50000 KG 20160729 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
126055131 12605513 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 .5 DF TABLET QOD
126055131 12605513 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD
126055131 12605513 3 C ESTRACE ESTRADIOL 1 0
126055131 12605513 4 C PROVERA MEDROXYPROGESTERONE ACETATE 1 0
126055131 12605513 5 C RANITIDINE. RANITIDINE 1 0
126055131 12605513 6 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 0
126055131 12605513 7 C HEART MEDS 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126055131 12605513 1 Blood cholesterol increased
126055131 12605513 2 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126055131 12605513 Blood cholesterol increased
126055131 12605513 Malaise
126055131 12605513 Off label use
126055131 12605513 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
126055131 12605513 1 2011 201506 0
126055131 12605513 2 201506 0
126055131 12605513 3 2001 0
126055131 12605513 4 2001 0