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
104827864 10482786 4 F 20140617 20160927 20140929 20160930 EXP GB-ASTRAZENECA-2014SE47060 ASTRAZENECA 25890.00 DY M Y 93.00000 KG 20160930 MD GB GB

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
104827864 10482786 1 PS LISINOPRIL. LISINOPRIL 1 Oral Y 0 TABLET
104827864 10482786 2 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Oral 25275 MG Y U 0 75 MG TABLET QD
104827864 10482786 3 SS FELODIPINE. FELODIPINE 1 Oral Y 0
104827864 10482786 4 SS DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 Oral Y 0
104827864 10482786 5 SS BENDROFLUMETHIAZIDE (NON AZ PRODUCT) BENDROFLUMETHIAZIDE 1 Oral Y 0
104827864 10482786 6 C SIMVASTATIN. SIMVASTATIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104827864 10482786 1 Hypertension
104827864 10482786 2 Peripheral arterial occlusive disease
104827864 10482786 3 Hypertension
104827864 10482786 4 Hypertension
104827864 10482786 5 Diuretic therapy
104827864 10482786 6 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
104827864 10482786 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104827864 10482786 Renal tubular necrosis

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
104827864 10482786 1 20031222 20140621 0
104827864 10482786 2 20130716 20140617 0
104827864 10482786 3 20031222 20140621 0
104827864 10482786 4 20031222 20140621 0
104827864 10482786 5 20101110 20140621 0
104827864 10482786 6 20070420 20140621 0