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
125841481 12584148 1 I 20160627 20160715 20160722 20160722 EXP IT-ASTRAZENECA-2016SE77993 ASTRAZENECA 3734.00 WK F Y 0.00000 20160722 MD IT IT

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
125841481 12584148 1 PS BRILIQUE TICAGRELOR 1 Oral 3960 MG Y U 22433 180 MG TABLET QD
125841481 12584148 2 SS CARDIOASPIRIN ASPIRIN 1 Unknown 22 DF U U 0 1 DF QD
125841481 12584148 3 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Intravenous (not otherwise specified) 4400 MG 0 4400 MG QD
125841481 12584148 4 C PANTORC PANTOPRAZOLE SODIUM 1 0
125841481 12584148 5 C TORVAST ATORVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125841481 12584148 1 Antiplatelet therapy
125841481 12584148 2 Antiplatelet therapy

Outcome of event

Event ID CASEID OUTC COD
125841481 12584148 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125841481 12584148 C-reactive protein abnormal
125841481 12584148 Eosinophilia
125841481 12584148 Pyrexia
125841481 12584148 Renal failure

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
125841481 12584148 1 20160606 20160629 0
125841481 12584148 2 20160606 0
125841481 12584148 3 20160627 20160630 0