The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7584537 8017524 I 7584537-2 20110408 20110621 20110630 EXP JP-PFIZER INC-2011146519 PFIZERINC 62 YR M Y 71.7 KG 20110630 MD JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7584537 1016908450 C NORVASC 1 ORAL UNK
7584537 1016908447 C ASPIRIN 1 ORAL UNK
7584537 1016908445 PS ATORVASTATIN CALCIUM 1 ORAL 20 MG, 1X/DAY 020702
7584537 1016908451 C SIGMART 2 ORAL UNK
7584537 1016908452 C RABEPRAZOLE SODIUM 1 ORAL UNK
7584537 1016908446 SS ATORVASTATIN CALCIUM 1 ORAL 10 MG, 1X/DAY 020702
7584537 1016908448 C MICARDIS 1 ORAL UNK
7584537 1016908449 C PLAVIX 1 ORAL UNK
7584537 1016908453 C ALLOPURINOL 2 ORAL UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7584537 1016908450 HYPERTENSION
7584537 1016908447 ANGINA PECTORIS
7584537 1016908445 HYPERCHOLESTEROLAEMIA
7584537 1016908451 ANGINA PECTORIS
7584537 1016908448 HYPERTENSION
7584537 1016908449 ANGINA PECTORIS
7584537 1016908453 HYPERURICAEMIA

Outcome of event

Event ID OUTC COD
7584537 HO

Reactions reported

Event ID PT
7584537 CHOLANGITIS
7584537 BILE DUCT STONE

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7584537 1016908445 20101116 20101206 21 DAY
7584537 1016908452 20101119
7584537 1016908446 20101207 20110408 123 DAY
7584537 1016908448 20101116
7584537 1016908449 20101116 20110215 92 DAY