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
6759420 7418030 I 6759420-2 20100527 20100603 EXP TPA2010A03298 TAKEDA PHARMACEUTICALS NORTH AMERICA 53 YR M N 20100602 OT UNITED STATES

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
6759420 1013822456 PS ACTOS 1 ORAL 45 MG, 1 IN 1 D, PER ORAL D D 21073
6759420 1013855191 SS LANTUS 1
6759420 1013855192 C LIPITOR 1
6759420 1013855193 C DIOVAN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6759420 1013822456 TYPE 2 DIABETES MELLITUS
6759420 1013855191 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6759420 OT
6759420 RI

Reactions reported

Event ID PT
6759420 CONVULSION
6759420 DRUG INEFFECTIVE
6759420 HYPOGLYCAEMIA

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

Event ID RPSR COD
6759420 CR
6759420 HP

Therapies reported

no results found