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
6795630 7423807 F 6795630-6 20100602 20100617 20100625 EXP JP-MERCK-1006USA01730 MERCK HUMAN HEALTH DIVISION 77 YR M Y 62 KG 20100625 MD JAPAN

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
6795630 1013957390 PS JANUVIA 1 ORAL 21995
6795630 1013957391 SS AMARYL 1 ORAL
6795630 1013957392 SS AMARYL 1 ORAL
6795630 1013957393 SS ACTOS 1 ORAL
6795630 1013957394 C MICARDIS 1 ORAL
6795630 1013957395 C ATELEC 2 ORAL
6795630 1013957396 SS GLYCORAN 2 ORAL
6795630 1013957397 SS GLUCOBAY 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6795630 1013957390 DIABETES MELLITUS
6795630 1013957391 DIABETES MELLITUS
6795630 1013957393 DIABETES MELLITUS
6795630 1013957394 HYPERTENSION
6795630 1013957395 HYPERTENSION
6795630 1013957396 DIABETES MELLITUS
6795630 1013957397 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6795630 LT
6795630 OT

Reactions reported

Event ID PT
6795630 FEMUR FRACTURE
6795630 HYPOGLYCAEMIA

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
6795630 1013957390 20100525
6795630 1013957391 20100512 20100525 14 DAY
6795630 1013957392 20100525
6795630 1013957393 20040625
6795630 1013957394 20061005
6795630 1013957395 20061006
6795630 1013957396 20040310
6795630 1013957397 20100312