The Safety Rates Drug Report

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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
73426033 7342603 3 F 20100321 20160824 20100402 20160901 EXP UA-PFIZER INC-2010036937 PFIZER 66.00 YR M Y 94.00000 KG 20160901 MD UA UA

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
73426033 7342603 1 PS CELECOXIB. CELECOXIB 1 Oral UNK Y 20998 CAPSULE, HARD
73426033 7342603 2 SS CELECOXIB. CELECOXIB 1 Y 20998 CAPSULE, HARD
73426033 7342603 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 20 MG, 1X/DAY 14480 MG 0 20 MG QD
73426033 7342603 4 C LISINOPRIL. LISINOPRIL 1 Oral 10 MG, 1X/DAY 0 10 MG QD
73426033 7342603 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, 1X/DAY 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73426033 7342603 1 Osteoarthritis
73426033 7342603 2 Rheumatoid arthritis
73426033 7342603 3 Prophylaxis
73426033 7342603 4 Hypertension
73426033 7342603 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
73426033 7342603 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
73426033 7342603 Atrial fibrillation

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
73426033 7342603 1 20080327 20100320 0
73426033 7342603 3 20080327 20100320 0
73426033 7342603 4 2007 0
73426033 7342603 5 2007 0