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
77940334 7794033 4 F 20100726 20160824 20110201 20160831 EXP TW-ASTRAZENECA-2011SE05041 ASTRAZENECA 74.00 YR M Y 110.00000 KG 20160901 MD TW TW

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
77940334 7794033 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 37240 MG Y 0 40 MG QD
77940334 7794033 2 SS NAPROXEN. NAPROXEN 1 Oral Y 0 TABLET
77940334 7794033 3 SS NAPROXEN. NAPROXEN 1 Oral Y 0 TABLET
77940334 7794033 4 C APROVEL IRBESARTAN 1 Unknown 0
77940334 7794033 5 C COLCHICINE. COLCHICINE 1 Unknown 0
77940334 7794033 6 C AMARYL GLIMEPIRIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77940334 7794033 2 Osteoarthritis
77940334 7794033 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
77940334 7794033 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
77940334 7794033 Coronary artery disease

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
77940334 7794033 1 20080108 20100816 0
77940334 7794033 2 20080108 20100816 0
77940334 7794033 3 20080108 20100816 0
77940334 7794033 4 20060207 0
77940334 7794033 5 20060207 0
77940334 7794033 6 20081209 0