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
6750603 7406426 I 6750603-4 20100113 20100518 20100601 EXP DE-MYLANLABS-2010S1008830 MYLAN PHARMACEUTICALS INC. 54 YR M Y 83 KG 20100601 OT 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
6750603 1013789610 SS METFORMIN HCL 1 ORAL
6750603 1013789611 PS ALLOPURINOL 1 ORAL 018659
6750603 1013789612 SS CRESTOR 1 ORAL
6750603 1013789613 SS JANUMET 1 ORAL EINE DF ENTHALT: 50 MG SITAGLIPTIN/1000 MG METFORMIN HYDROCHLORIDE
6750603 1013789614 SS ACTOS 1 ORAL
6750603 1013789615 SS OMACOR 1 ORAL
6750603 1013789616 SS RASILEZ /01763601/ 2 ORAL
6750603 1013789617 C RAMIPRIL 2 ORAL
6750603 1013789618 C METOHEXAL SUCC 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6750603 1013789610 TYPE 2 DIABETES MELLITUS
6750603 1013789611 HYPERURICAEMIA
6750603 1013789612 HYPERLIPIDAEMIA
6750603 1013789613 TYPE 2 DIABETES MELLITUS
6750603 1013789614 TYPE 2 DIABETES MELLITUS
6750603 1013789615 HYPERTRIGLYCERIDAEMIA
6750603 1013789616 HYPERTENSION
6750603 1013789617 HYPERTENSION
6750603 1013789618 HYPERTENSION

Outcome of event

Event ID OUTC COD
6750603 HO

Reactions reported

Event ID PT
6750603 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
6750603 1013789610 20080701 20100422
6750603 1013789611 20100423
6750603 1013789612 20091008 20100423
6750603 1013789613 20090101 20100423
6750603 1013789614 20090713 20100423
6750603 1013789615 20080701 20100423
6750603 1013789616 20070101 20100423
6750603 1013789617 20051001
6750603 1013789618 20051001