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
6786559 7429268 F 6786559-8 20100127 20100615 20100623 EXP JP-MERCK-1004USA04013 MERCK HUMAN HEALTH DIVISION 65 YR F Y 20100623 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
6786559 1013923745 PS JANUVIA 1 ORAL 021995
6786559 1013923746 SS AMARYL 1 ORAL
6786559 1013923747 SS AMARYL 1 ORAL
6786559 1013923748 SS ACTOS 1 ORAL
6786559 1013923749 C ASPIRIN 1 UNKNOWN
6786559 1013923750 C PROSNER 2 UNKNOWN
6786559 1013923751 C NATRIX 2 UNKNOWN
6786559 1013923752 C MICARDIS 1 UNKNOWN
6786559 1013923753 C SUNRYTHM 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6786559 1013923745 TYPE 2 DIABETES MELLITUS
6786559 1013923746 TYPE 2 DIABETES MELLITUS
6786559 1013923748 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6786559 HO

Reactions reported

Event ID PT
6786559 ALTERED STATE OF CONSCIOUSNESS
6786559 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
6786559 1013923745 20091225 20100127 34 DAY
6786559 1013923746 20100128
6786559 1013923747 20100127
6786559 1013923748 20100127