The Safety Rates Drug Report

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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
6710202 7380711 I 6710202-7 20100401 20100416 20100430 EXP TCI2010A01499 TAKEDA PHARMACEUTICALS NORTH AMERICA. YR M N 20100429 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
6710202 1013623250 PS BASEN (VOGLIBOSE) 2 ORAL 15 MG (15 MG, 1-2), PER ORAL D 21073
6710202 1013647018 SS ACTOS 1 ORAL PER ORAL
6710202 1013647020 SS AMARYL 1 ORAL 3 MG (3 MG, 1 D), PER ORAL
6710202 1013647022 SS GLACTIV (SITAGLIPTIN PHOSPHATE HYDRATE) (ORAL ANTIDIABETICS) 2 ORAL PER ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6710202 1013623250 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6710202 HO

Reactions reported

Event ID PT
6710202 HYPOGLYCAEMIC COMA

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
6710202 FGN
6710202 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6710202 1013623250 20100413