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
6744317 7401716 F 6744317-4 20100112 20100520 20100527 EXP JP-MERCK-1003USA01127 MERCK HUMAN HEALTH DIVISION 55 YR F Y 47 KG 20100527 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
6744317 1013763465 PS JANUVIA 1 ORAL 021995
6744317 1013763466 C AMLODIPINE BESYLATE 2 ORAL
6744317 1013763467 C PLETAL 1 ORAL
6744317 1013763468 C NITROPEN 2 ORAL
6744317 1013763469 C MICARDIS 1 ORAL
6744317 1013763470 C MICARDIS 1 ORAL
6744317 1013763471 SS ACTOS 1 ORAL
6744317 1013763472 C CRESTOR 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6744317 1013763465 TYPE 2 DIABETES MELLITUS
6744317 1013763466 HYPERTENSION
6744317 1013763469 HYPERTENSION
6744317 1013763471 TYPE 2 DIABETES MELLITUS
6744317 1013763472 DYSLIPIDAEMIA

Outcome of event

Event ID OUTC COD
6744317 OT

Reactions reported

Event ID PT
6744317 DYSPEPSIA

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
6744317 1013763465 20091225 20100223 61 DAY
6744317 1013763466 20080717
6744317 1013763469 20080717
6744317 1013763470 20080613
6744317 1013763471 20080717
6744317 1013763472 20090327