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
6735058 7366310 F 6735058-8 20060601 20100510 20100521 EXP GB-PFIZER INC-2010046275 PFIZERINC 72 YR F Y 96.4 KG 20100520 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
6735058 1013726219 PS ATORVASTATIN CALCIUM 2 UNK 20702
6735058 1013726220 SS SIMVASTATIN 2 ORAL UNK
6735058 1013726221 SS ACTOS 1 30 MG, 1X/DAY
6735058 1013726222 SS ROSIGLITAZONE 2 4 MG, 1X/DAY
6735058 1013726223 SS ROSIGLITAZONE 2 8 MG, 1X/DAY
6735058 1013726224 SS SUPRALIP 2 160 MG, 1X/DAY
6735058 1013726225 SS SUPRALIP 2 UNK
6735058 1013726226 C METFORMIN 2 1.5 G, DAILY
6735058 1013726227 C ROSUVASTATIN 2 10 MG, UNK
6735058 1013726228 C ROSUVASTATIN 2 20 MG, UNK
6735058 1013726229 C ROSUVASTATIN 2 10 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6735058 1013726221 TYPE 2 DIABETES MELLITUS
6735058 1013726222 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6735058 OT

Reactions reported

Event ID PT
6735058 HIGH DENSITY LIPOPROTEIN DECREASED
6735058 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
6735058 1013726219 20040201
6735058 1013726221 20070201 20070501
6735058 1013726222 20050301 20050601
6735058 1013726223 20050601 20060901
6735058 1013726224 20030501 20060901
6735058 1013726225 20060901
6735058 1013726227 20040201 20050601
6735058 1013726228 20050601 20060801
6735058 1013726229 20060801