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
6731004 7366310 F 6731004-1 20060601 20100510 20100518 EXP GB-PFIZER INC-2010046275 PFIZERINC 72 YR F Y 96.4 KG 20100517 UNITED KINGDOM

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
6731004 1013709816 PS ATORVASTATIN CALCIUM 1 UNK 20702
6731004 1013709817 SS SIMVASTATIN 1 ORAL UNK
6731004 1013709818 SS ACTOS 1 30 MG, 1X/DAY
6731004 1013709819 SS ROSIGLITAZONE 2 4 MG, 1X/DAY
6731004 1013709820 SS ROSIGLITAZONE 2 8 MG, 1X/DAY
6731004 1013709821 SS SUPRALIP 2 160 MG, 1X/DAY
6731004 1013709822 SS SUPRALIP 2 UNK
6731004 1013709823 C METFORMIN 2 1.5 G, DAILY
6731004 1013709824 C ROSUVASTATIN 2 10 MG, UNK
6731004 1013709825 C ROSUVASTATIN 2 20 MG, UNK
6731004 1013709826 C ROSUVASTATIN 2 10 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6731004 1013709818 TYPE 2 DIABETES MELLITUS
6731004 1013709819 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6731004 OT

Reactions reported

Event ID PT
6731004 HIGH DENSITY LIPOPROTEIN DECREASED
6731004 MYALGIA

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
6731004 1013709816 20040201
6731004 1013709818 20070201 20070501
6731004 1013709819 20050301 20050601
6731004 1013709820 20050601 20060901
6731004 1013709821 20030501 20060901
6731004 1013709822 20060901
6731004 1013709824 20040201 20050601
6731004 1013709825 20050601 20060801
6731004 1013709826 20060801