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
6698884 7293496 F 6698884-X 20100131 20100408 20100427 EXP JP-MERCK-1002USA03442 MERCK HUMAN HEALTH DIVISION 81 YR F Y 20100427 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
6698884 1013578411 PS JANUVIA 1 ORAL 021995
6698884 1013578412 SS AMARYL 1 ORAL
6698884 1013578413 SS AMARYL 1 ORAL
6698884 1013578414 SS AMARYL 1 ORAL
6698884 1013578415 SS ACTOS 1 ORAL
6698884 1013578416 C RIVOTRIL 2 UNKNOWN
6698884 1013578417 C LIVALO 1 UNKNOWN
6698884 1013578418 C CANDESARTAN CILEXETIL 1 UNKNOWN
6698884 1013578419 C AMLODIPINE BESYLATE 2 UNKNOWN
6698884 1013578420 C PEPCID 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6698884 1013578411 TYPE 2 DIABETES MELLITUS
6698884 1013578412 TYPE 2 DIABETES MELLITUS
6698884 1013578415 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6698884 OT

Reactions reported

Event ID PT
6698884 ALTERED STATE OF CONSCIOUSNESS
6698884 BALANCE DISORDER
6698884 CHILLS
6698884 DYSARTHRIA
6698884 GAIT DISTURBANCE
6698884 HYPOGLYCAEMIA
6698884 MUSCULAR WEAKNESS

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
6698884 1013578411 20091217 20100131 46 DAY
6698884 1013578413 20100203
6698884 1013578414 20100131
6698884 1013578416 20080122
6698884 1013578417 20080120
6698884 1013578418 20081212
6698884 1013578419 20080120