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
6686098 7366610 I 6686098-9 20090310 20100407 20100414 EXP TCI2009A04361 TAKEDA PHARMACEUTICALS NORTH AMERICA. 76 YR F N 20100413 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
6686098 1013523649 PS ACTOS 1 ORAL 15 MG (15 MG,1 IN 1 D) PER ORAL Y D 21073
6686098 1013571636 C BASEN OD (VOGLIBOSE) 2
6686098 1013571637 C BIGUANDIES 2
6686098 1013571638 C PARIET (RABEPROZOLE SODIUM) 2
6686098 1013571639 C CRESTOR 1
6686098 1013571641 C LOSARTAN POTASSIUM 1
6686098 1013571642 C SULFONAMIDES, UREA DERIVATIVES 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6686098 1013523649 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6686098 HO

Reactions reported

Event ID PT
6686098 ANGER
6686098 ANXIETY
6686098 ATRIAL FIBRILLATION
6686098 BLOOD PRESSURE INCREASED
6686098 CARDIAC FAILURE CHRONIC
6686098 DECREASED APPETITE
6686098 PARANOIA
6686098 PSYCHIATRIC SYMPTOM
6686098 PULMONARY CONGESTION
6686098 WEIGHT DECREASED

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

Event ID RPSR COD
6686098 FGN
6686098 HP
6686098 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6686098 1013523649 20080331 20090420 384 DAY