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
124908372 12490837 2 F 20101220 20160803 20160623 20160811 EXP DK-ASTRAZENECA-2016SE65449 ASTRAZENECA 19598.00 DY F Y 56.00000 KG 20160811 CN DK DK

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
124908372 12490837 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 39240 MG U U 21366 20 MG TABLET QD
124908372 12490837 2 C ANCOZAN LOSARTAN POTASSIUM 1 0
124908372 12490837 3 C CLORIOCARD 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124908372 12490837 1 Hypercholesterolaemia
124908372 12490837 3 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124908372 12490837 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124908372 12490837 Cupulolithiasis
124908372 12490837 Dizziness
124908372 12490837 Insomnia
124908372 12490837 Nausea
124908372 12490837 Thrombosis

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
124908372 12490837 1 20101215 20160429 0