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
6748531 7405113 I 6748531-3 20100113 20100518 20100601 EXP DE-RANBAXY-2010RR-34055 RANBAXYUS 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
6748531 1013781183 SS ALLOPURINOL 1 ORAL 150 MG, QD
6748531 1013781184 PS METFORMIN HCL 1 ORAL 500 MG, QD 021591
6748531 1013781185 SS CRESTOR 1 ORAL 10 MG, QD
6748531 1013781186 SS JANUMET 1 ORAL 1 DF, UNK
6748531 1013781187 SS ACTOS 1 ORAL 15 MG, QD
6748531 1013781188 SS OMACOR 1 ORAL UNK
6748531 1013781189 SS RASILEZ 2 ORAL 150 MG, QD
6748531 1013781190 C RAMIPRIL 1 ORAL 5 MG, QD
6748531 1013781191 C METOHEXAL SUCC 95MG 2 ORAL 47.5 MG, QD

Indications of drugs used

Event ID DRUG SEQ INDI PT
6748531 1013781183 HYPERURICAEMIA
6748531 1013781184 TYPE 2 DIABETES MELLITUS
6748531 1013781185 HYPERLIPIDAEMIA
6748531 1013781186 TYPE 2 DIABETES MELLITUS
6748531 1013781187 TYPE 2 DIABETES MELLITUS
6748531 1013781188 HYPERTRIGLYCERIDAEMIA
6748531 1013781189 HYPERTENSION
6748531 1013781190 HYPERTENSION
6748531 1013781191 HYPERTENSION

Outcome of event

Event ID OUTC COD
6748531 HO

Reactions reported

Event ID PT
6748531 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
6748531 1013781183 20100423
6748531 1013781184 20080701 20100422
6748531 1013781185 20091008 20100423 198 DAY
6748531 1013781186 20090101 20100423
6748531 1013781187 20090713 20100423 285 DAY
6748531 1013781188 20080701 20100423
6748531 1013781189 20070101 20100423
6748531 1013781190 20051001
6748531 1013781191 20051001