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
6694581 7293496 F 6694581-5 20100131 20100416 20100423 EXP JP-MERCK-1002USA03442 MERCK HUMAN HEALTH DIVISION 81 YR F Y 20100423 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
6694581 1013558718 PS JANUVIA 1 ORAL 021995
6694581 1013558719 SS AMARYL 1 ORAL
6694581 1013558720 SS AMARYL 1 ORAL
6694581 1013558721 SS AMARYL 1 ORAL
6694581 1013558722 SS ACTOS 1 ORAL
6694581 1013558723 C CLONAZEPAM 1 UNKNOWN
6694581 1013558724 C LIVALO 1 UNKNOWN
6694581 1013558725 C CANDESARTAN CILEXETIL 1 UNKNOWN
6694581 1013558726 C AMLODIPINE BESYLATE 2 UNKNOWN
6694581 1013558727 C PEPCID 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6694581 1013558718 TYPE 2 DIABETES MELLITUS
6694581 1013558719 TYPE 2 DIABETES MELLITUS
6694581 1013558722 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6694581 OT

Reactions reported

Event ID PT
6694581 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
6694581 1013558718 20091217 20100131 46 DAY
6694581 1013558720 20100203
6694581 1013558721 20100131
6694581 1013558723 20080122
6694581 1013558724 20080120
6694581 1013558725 20081212
6694581 1013558726 20080120