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
6696853 7374787 I 6696853-7 20100415 20100422 EXP TUK2010A00054 TAKEDA PHARMACEUTICALS NORTH AMERICA. 54 YR F N 20100421 UNITED KINGDOM

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
6696853 1013569006 PS ACTOS 1 ORAL (15 MG) ORAL Y 21073
6696853 1013615149 C METFORMIN HCL 1
6696853 1013615150 C NAPROXEN 1
6696853 1013615151 C SIMVASTATIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6696853 1013569006 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6696853 OT
6696853 RI

Reactions reported

Event ID PT
6696853 ARTHRALGIA
6696853 HYPOAESTHESIA
6696853 JOINT SWELLING

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

Event ID RPSR COD
6696853 FGN
6696853 HP
6696853 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6696853 1013569006 20091104 20100320 136 DAY