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
6677266 7323128 F 2 6677266-0 20091201 20100323 20100408 EXP THQ2010A00433 TAKEDA PHARMACEUTICALS NORTH AMERICA 49 YR F N 20100407 OT 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
6677266 1013484334 PS ACTOS 1 15 MG (15 MG,1 IN 1 D) Y U 21073
6677266 1013543881 SS BYETTA 1 SUBCUTANEOUS SEE IMAGE
6677266 1013543882 SS GLUCOPHAGE 1 2.55 GM (2.55 GM,1 IN 1 D) ; 2.55 GM (2.55 GM,1 IN 1 D)

Indications of drugs used

Event ID DRUG SEQ INDI PT
6677266 1013484334 TYPE 2 DIABETES MELLITUS
6677266 1013543881 TYPE 2 DIABETES MELLITUS
6677266 1013543882 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6677266 HO

Reactions reported

Event ID PT
6677266 ABDOMINAL PAIN LOWER
6677266 SALPINGO-OOPHORECTOMY BILATERAL

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
6677266 FGN
6677266 HP
6677266 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6677266 1013484334 20091112 20091201 19 DAY
6677266 1013543881 20070524 20070621 28 DAY
6677266 1013543881 20070622 20091201 893 DAY
6677266 1013543881 20091203
6677266 1013543882 20060501 20091201 3 YR
6677266 1013543882 20091203