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
6763468 7418030 F 1 6763468-1 20100527 20100608 EXP TPA2010A03298 TAKEDA PHARMACEUTICALS NORTH AMERICA. 53 YR M N 20100607 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
6763468 1013838629 PS ACTOS 1 ORAL 45 MG, 1 IN 1 D, PER ORAL D D 21073
6763468 1013871579 SS LANTUS 1
6763468 1013871581 C LIPITOR 1
6763468 1013871582 C DIOVAN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6763468 1013838629 TYPE 2 DIABETES MELLITUS
6763468 1013871579 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6763468 OT
6763468 RI

Reactions reported

Event ID PT
6763468 CONVULSION
6763468 HYPOGLYCAEMIA
6763468 NO THERAPEUTIC RESPONSE

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

Event ID RPSR COD
6763468 CR
6763468 HP

Therapies reported

no results found