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
6750607 7406426 I 6750607-1 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
6750607 1013789636 PS METFORMIN HCL 1 ORAL 75973
6750607 1013789637 SS ALLOPURINOL 1 ORAL
6750607 1013789638 SS CRESTOR 1 ORAL
6750607 1013789639 SS JANUMET 1 ORAL EINE DF ENTHALT: 50 MG SITAGLIPTIN/1000 MG METFORMIN HYDROCHLORIDE
6750607 1013789640 SS ACTOS 1 ORAL
6750607 1013789641 SS OMACOR 1 ORAL
6750607 1013789642 SS RASILEZ /01763601/ 2 ORAL
6750607 1013789643 C RAMIPRIL 2 ORAL
6750607 1013789644 C METOHEXAL SUCC 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6750607 1013789636 TYPE 2 DIABETES MELLITUS
6750607 1013789637 HYPERURICAEMIA
6750607 1013789638 HYPERLIPIDAEMIA
6750607 1013789639 TYPE 2 DIABETES MELLITUS
6750607 1013789640 TYPE 2 DIABETES MELLITUS
6750607 1013789641 HYPERTRIGLYCERIDAEMIA
6750607 1013789642 HYPERTENSION
6750607 1013789643 HYPERTENSION
6750607 1013789644 HYPERTENSION

Outcome of event

Event ID OUTC COD
6750607 HO

Reactions reported

Event ID PT
6750607 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
6750607 1013789636 20080701 20100422
6750607 1013789637 20100423
6750607 1013789638 20091008 20100423
6750607 1013789639 20090101 20100423
6750607 1013789640 20090713 20100423
6750607 1013789641 20080701 20100423
6750607 1013789642 20070101 20100423
6750607 1013789643 20051001
6750607 1013789644 20051001