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
6750604 7406426 I 6750604-6 20100113 20100518 20100601 EXP DE-MYLANLABS-2010S1008830 ALPHAPHARM 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
6750604 1013789619 PS METFORMIN HCL 1 ORAL 75969
6750604 1013789620 SS ALLOPURINOL 1 ORAL
6750604 1013789621 SS CRESTOR 1 ORAL
6750604 1013789622 SS JANUMET 1 ORAL EINE DF ENTHALT: 50 MG SITAGLIPTIN/1000 MG METFORMIN HYDROCHLORIDE
6750604 1013789623 SS ACTOS 1 ORAL
6750604 1013789624 SS OMACOR 1 ORAL
6750604 1013789625 SS RASILEZ /01763601/ 2 ORAL
6750604 1013789626 C RAMIPRIL 2 ORAL
6750604 1013789627 C METOHEXAL SUCC 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6750604 1013789619 TYPE 2 DIABETES MELLITUS
6750604 1013789620 HYPERURICAEMIA
6750604 1013789621 HYPERLIPIDAEMIA
6750604 1013789622 TYPE 2 DIABETES MELLITUS
6750604 1013789623 TYPE 2 DIABETES MELLITUS
6750604 1013789624 HYPERTRIGLYCERIDAEMIA
6750604 1013789625 HYPERTENSION
6750604 1013789626 HYPERTENSION
6750604 1013789627 HYPERTENSION

Outcome of event

Event ID OUTC COD
6750604 HO

Reactions reported

Event ID PT
6750604 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
6750604 1013789619 20080701 20100422
6750604 1013789620 20100423
6750604 1013789621 20091008 20100423
6750604 1013789622 20090101 20100423
6750604 1013789623 20090713 20100423
6750604 1013789624 20080701 20100423
6750604 1013789625 20070101 20100423
6750604 1013789626 20051001
6750604 1013789627 20051001