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
6781498 7366310 F 6781498-0 20060601 20100611 20100621 EXP GB-PFIZER INC-2010046275 PFIZERINC 72 YR F Y 96.4 KG 20100618 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
6781498 1013903550 PS ATORVASTATIN CALCIUM 1 UNK 20702
6781498 1013903551 SS SIMVASTATIN 1 ORAL UNK
6781498 1013903552 SS ACTOS 1 30 MG, 1X/DAY
6781498 1013903553 SS ROSIGLITAZONE 2 4 MG, 1X/DAY
6781498 1013903554 SS ROSIGLITAZONE 2 8 MG, 1X/DAY
6781498 1013903555 SS SUPRALIP 2 160 MG, 1X/DAY
6781498 1013903556 SS SUPRALIP 2 UNK
6781498 1013903557 C METFORMIN 2 1.5 G, DAILY
6781498 1013903558 C ROSUVASTATIN 2 10 MG, UNK
6781498 1013903559 C ROSUVASTATIN 2 20 MG, UNK
6781498 1013903560 C ROSUVASTATIN 2 10 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6781498 1013903552 TYPE 2 DIABETES MELLITUS
6781498 1013903553 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6781498 OT

Reactions reported

Event ID PT
6781498 BLOOD TRIGLYCERIDES INCREASED
6781498 DIABETES MELLITUS INADEQUATE CONTROL
6781498 GLYCOSYLATED HAEMOGLOBIN INCREASED
6781498 HIGH DENSITY LIPOPROTEIN DECREASED
6781498 INSULIN RESISTANCE
6781498 MYALGIA
6781498 PARADOXICAL DRUG REACTION

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
6781498 1013903550 20040201
6781498 1013903552 20070201 20070501
6781498 1013903553 20050301 20050601
6781498 1013903554 20050601 20060901
6781498 1013903555 20030501 20060901
6781498 1013903556 20060901
6781498 1013903558 20040201 20050601
6781498 1013903559 20050601 20060801
6781498 1013903560 20060801