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
6752632 7407782 I 6752632-3 20100113 20100521 20100602 EXP DE-WATSON-2010-07118 WATSON YR Y 20100602 CN UNITED KINGDOM

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
6752632 1013796921 PS METFORMIN HCL 1 ORAL 500 MG, DAILY UNCONFIRMED 76818
6752632 1013796922 SS CRESTOR 1 ORAL 10 MG, DAILY
6752632 1013796923 SS JANUMET 1 ORAL 1 DF, BID
6752632 1013796924 SS ACTOS 1 ORAL 15 MG, DAILY
6752632 1013796925 SS OMACOR 1 ORAL 1000 MG, QID
6752632 1013796926 SS ALLOPURINOL 1 ORAL 150 MG, DAILY
6752632 1013796927 SS RASILEZ 2 ORAL 150 MG, DAILY
6752632 1013796928 C RAMIPRIL 2 ORAL 5 MG, DAILY
6752632 1013796929 C METOHEXAL SUCC 2 ORAL 47 1/2 MG, DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6752632 1013796921 TYPE 2 DIABETES MELLITUS
6752632 1013796922 HYPERLIPIDAEMIA
6752632 1013796923 TYPE 2 DIABETES MELLITUS
6752632 1013796924 TYPE 2 DIABETES MELLITUS
6752632 1013796925 HYPERTRIGLYCERIDAEMIA
6752632 1013796926 HYPERURICAEMIA
6752632 1013796927 HYPERTENSION
6752632 1013796928 HYPERTENSION
6752632 1013796929 HYPERTENSION

Outcome of event

Event ID OUTC COD
6752632 HO

Reactions reported

Event ID PT
6752632 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
6752632 1013796921 20080701 20100422
6752632 1013796922 20091008 20100423 198 DAY
6752632 1013796923 20090101 20100423
6752632 1013796924 20090713 20100423 285 DAY
6752632 1013796925 20080701 20100423
6752632 1013796926 20100423
6752632 1013796927 20070101 20100423
6752632 1013796928 20051001
6752632 1013796929 20051001