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
6743387 7401102 I 6743387-7 20100113 20100519 20100527 EXP DE-ASTRAZENECA-2010SE23405 AZPRODUW00 54 YR M Y 83 KG 20100527 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
6743387 1013759608 PS CRESTOR 1 ORAL 21366
6743387 1013759609 SS METFORMIN HYDROCHLORIDE 1 ORAL
6743387 1013759610 SS JANUMET 1 ORAL
6743387 1013759611 SS ACTOS 1 ORAL
6743387 1013759612 SS OMACOR 1 ORAL
6743387 1013759613 SS ALLOPURINOL 1 ORAL
6743387 1013759614 SS RASILEZ 2 ORAL
6743387 1013759615 C RAMIPRIL 1 ORAL
6743387 1013759616 C METOHEXAL SUCC 95 MG 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6743387 1013759608 HYPERLIPIDAEMIA
6743387 1013759609 TYPE 2 DIABETES MELLITUS
6743387 1013759610 TYPE 2 DIABETES MELLITUS
6743387 1013759611 TYPE 2 DIABETES MELLITUS
6743387 1013759612 HYPERTRIGLYCERIDAEMIA
6743387 1013759613 HYPERURICAEMIA
6743387 1013759614 HYPERTENSION
6743387 1013759615 HYPERTENSION
6743387 1013759616 HYPERTENSION

Outcome of event

Event ID OUTC COD
6743387 HO

Reactions reported

Event ID PT
6743387 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
6743387 1013759608 20091008 20100423 198 DAY
6743387 1013759609 20080701 20100422 21 MON
6743387 1013759610 20090101 20100423 1 YR
6743387 1013759611 20090713 20100423 285 DAY
6743387 1013759612 20080701 20100423 21 MON
6743387 1013759613 20100423
6743387 1013759614 20070101 20100423 3 YR
6743387 1013759615 20051001
6743387 1013759616 20051001