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
119032265 11903226 5 F 20160229 20160517 20160110 20160714 PER US-ASTRAZENECA-2015SF31382 ASTRAZENECA 3284.00 WK M Y 101.60000 KG 20160714 CN 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
119032265 11903226 1 PS BRILINTA TICAGRELOR 1 Oral U U 22433 90 MG TABLET BID
119032265 11903226 2 SS BRILINTA TICAGRELOR 1 Oral U U 22433 90 MG TABLET BID
119032265 11903226 3 SS BRILINTA TICAGRELOR 1 Oral U U 22433 90 MG TABLET BID
119032265 11903226 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 TABLET
119032265 11903226 5 C COREG CARVEDILOL 1 0
119032265 11903226 6 C HYDROCODONE HYDROCODONE 1 0
119032265 11903226 7 C NIACIN. NIACIN 1 0
119032265 11903226 8 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119032265 11903226 1 Acute coronary syndrome
119032265 11903226 2 Myocardial infarction
119032265 11903226 3 Stent placement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119032265 11903226 Drug dose omission
119032265 11903226 Dyspnoea
119032265 11903226 Frustration tolerance decreased
119032265 11903226 Incorrect dose administered
119032265 11903226 Insomnia

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
119032265 11903226 1 20151211 0
119032265 11903226 2 20151211 0
119032265 11903226 3 20151211 0