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
127051751 12705175 1 I 20110224 20110330 20160831 20160831 EXP US-ASTRAZENECA-2016SE92385 ASTRAZENECA 63.00 YR F Y 76.20000 KG 20160901 MD 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
127051751 12705175 1 PS NAPROXEN. NAPROXEN 1 Oral Y U 0 TABLET
127051751 12705175 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral Y U 0
127051751 12705175 3 C JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 0
127051751 12705175 4 C AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 Oral 0
127051751 12705175 5 C VYTORIN EZETIMIBESIMVASTATIN 1 Oral 0
127051751 12705175 6 C ASPIRIN. ASPIRIN 1 Oral 0
127051751 12705175 7 C LANTUS INSULIN GLARGINE 1 Unknown 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127051751 12705175 1 Osteoarthritis
127051751 12705175 2 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
127051751 12705175 OT
127051751 12705175 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127051751 12705175 Myocardial infarction

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
127051751 12705175 1 20101001 20110223 0
127051751 12705175 2 20100930 20110223 0
127051751 12705175 3 2010 0
127051751 12705175 4 2004 20110224 0
127051751 12705175 5 2006 0
127051751 12705175 6 2008 0
127051751 12705175 7 201008 0