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
6754283 7405871 F 6754283-3 20100514 20100526 20100603 EXP JP-MERCK-1005USA03087 MERCK HUMAN HEALTH DIVISION 75 YR M Y 61 KG 20100603 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
6754283 1013803130 PS JANUVIA 1 ORAL 21995
6754283 1013803131 C AMLODIPINE 1 ORAL
6754283 1013803132 C YOKU-KAN-SAN-KA-CHIMPI-HANGE 2 ORAL
6754283 1013803133 C PLETAL 1 ORAL
6754283 1013803134 C ARICEPT 1 ORAL
6754283 1013803135 SS MELBIN 2 ORAL
6754283 1013803136 SS ACTOS 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6754283 1013803130 DIABETES MELLITUS
6754283 1013803131 HYPERTENSION
6754283 1013803133 CEREBRAL INFARCTION
6754283 1013803134 DEMENTIA ALZHEIMER'S TYPE
6754283 1013803135 DIABETES MELLITUS
6754283 1013803136 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6754283 OT

Reactions reported

Event ID PT
6754283 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
6754283 1013803130 20100426 20100514 19 DAY
6754283 1013803131 20100325 20100520 57 DAY
6754283 1013803132 20100325
6754283 1013803133 20100325 20100520 57 DAY
6754283 1013803134 20100408 20100520 43 DAY
6754283 1013803135 20100311 20100520 71 DAY
6754283 1013803136 20100520