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
6686741 7293496 F 6686741-4 20100131 20100408 20100419 EXP JP-MERCK-1002USA03442 MERCK HUMAN HEALTH DIVISION 81 YR F Y 20100419 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
6686741 1013526156 PS JANUVIA 1 ORAL 021995
6686741 1013526157 SS AMARYL 1 ORAL
6686741 1013526158 SS AMARYL 1 ORAL
6686741 1013526159 SS AMARYL 1 ORAL
6686741 1013526160 SS ACTOS 1 ORAL
6686741 1013526161 C CLONAZEPAM 1 UNKNOWN
6686741 1013526162 C LIVALO 1 UNKNOWN
6686741 1013526163 C CANDESARTAN CILEXETIL 1 UNKNOWN
6686741 1013526164 C AMLODIPINE BESYLATE 2 UNKNOWN
6686741 1013526165 C PEPCID 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6686741 1013526156 TYPE 2 DIABETES MELLITUS
6686741 1013526157 TYPE 2 DIABETES MELLITUS
6686741 1013526160 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6686741 OT

Reactions reported

Event ID PT
6686741 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
6686741 1013526156 20091217 20100131 46 DAY
6686741 1013526158 20100203
6686741 1013526159 20100131
6686741 1013526161 20080122
6686741 1013526162 20080120
6686741 1013526163 20081212
6686741 1013526164 20080120