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
6758724 7376392 F 6758724-7 20100307 20100528 20100607 EXP JP-MERCK-1004USA04793 MERCK HUMAN HEALTH DIVISION 87 YR F Y 20100607 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
6758724 1013819806 PS JANUVIA 1 ORAL 21995
6758724 1013819807 C CELECOX 2 ORAL
6758724 1013819808 SS FENOFIBRATE 1 ORAL
6758724 1013819809 C FUROSEMIDE 2 ORAL
6758724 1013819810 SS AMARYL 1 ORAL
6758724 1013819811 SS AMARYL 1 ORAL 3MG IN THE MORNING AND 2 IN THE EVENING
6758724 1013819812 SS AMARYL 1 ORAL
6758724 1013819813 SS MELBIN 2 ORAL
6758724 1013819814 SS SEIBULE 2 ORAL
6758724 1013819815 SS ACTOS 1 ORAL
6758724 1013819816 C ACTONEL 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6758724 1013819806 DIABETES MELLITUS
6758724 1013819807 OSTEOARTHRITIS
6758724 1013819809 OEDEMA
6758724 1013819810 DIABETES MELLITUS
6758724 1013819813 DIABETES MELLITUS
6758724 1013819814 DIABETES MELLITUS
6758724 1013819815 DIABETES MELLITUS
6758724 1013819816 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
6758724 HO

Reactions reported

Event ID PT
6758724 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
6758724 1013819806 20100216
6758724 1013819807 20071127
6758724 1013819808 20100216
6758724 1013819809 20071001
6758724 1013819810 20071001 20100311 893 DAY
6758724 1013819811 20100312 20100330 19 DAY
6758724 1013819812 20100331 20100408 9 DAY
6758724 1013819813 20071001 20100408 921 DAY
6758724 1013819814 20071001
6758724 1013819815 20090101
6758724 1013819816 20071027