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
6758838 7393294 F 6758838-1 20100113 20100604 20100607 EXP GXKR2010DE05440 SANDOZ,INC. 54 YR M Y 83 KG 20100607 MD GERMANY

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
6758838 1013820175 PS METFORMIN HCL 1 ORAL 500 MG, QD 75985
6758838 1013820176 SS ALLOPURINOL 1 ORAL 150 MG, QD
6758838 1013820177 SS CRESTOR 1 ORAL 10 MG, QD
6758838 1013820178 SS JANUMET 1 ORAL 1 DF, BID
6758838 1013820179 SS ACTOS 1 ORAL 15 MG, QD
6758838 1013820180 SS OMACOR 1 ORAL 1000 MG, QID
6758838 1013820181 SS RASILEZ (ALISKIREN) 2 ORAL 150 MG, QD
6758838 1013820182 C METOHEXAL 2 ORAL
6758838 1013820183 C RAMIPRIL 1
6758838 1013820184 C SIMVAHEXAL 2 40 MG, QD

Indications of drugs used

Event ID DRUG SEQ INDI PT
6758838 1013820175 TYPE 2 DIABETES MELLITUS
6758838 1013820176 HYPERURICAEMIA
6758838 1013820177 HYPERLIPIDAEMIA
6758838 1013820178 TYPE 2 DIABETES MELLITUS
6758838 1013820179 TYPE 2 DIABETES MELLITUS
6758838 1013820180 HYPERTRIGLYCERIDAEMIA
6758838 1013820181 HYPERTENSION
6758838 1013820184 HYPERLIPIDAEMIA

Outcome of event

Event ID OUTC COD
6758838 HO

Reactions reported

Event ID PT
6758838 LIVER INJURY

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
6758838 1013820175 20080701 20100422
6758838 1013820176 20100423
6758838 1013820177 20091008 20100423 198 DAY
6758838 1013820178 20090101 20100423
6758838 1013820179 20090713 20100423 285 DAY
6758838 1013820180 20080701 20100423
6758838 1013820181 20070101 20100423
6758838 1013820184 20091007