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
6694678 7366610 F 6694678-X 20090310 20100414 20100420 EXP TCI2009A04361 TAKEDA PHARMACEUTICALS NORTH AMERICA. 76 YR F N 20100419 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
6694678 1013559175 PS ACTOS 1 ORAL 15 MG (15 MG,1 IN 1 D) PER ORAL Y D 21073
6694678 1013596180 C BASEN OD (VOGLIBOSE) 2
6694678 1013596181 C BIGUANIDES 2
6694678 1013596183 C RABEPRAZOLE SODIUM 1
6694678 1013596197 C CRESTOR 1
6694678 1013596198 C LOSARTAN POTASSIUM 1
6694678 1013596199 C SULFONAMIDES, UREA DERIVATIVES 2
6694678 1013596200 C ANTITHROMBOTIC AGENTS 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6694678 1013559175 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6694678 HO

Reactions reported

Event ID PT
6694678 ANXIETY
6694678 ATRIAL FIBRILLATION
6694678 BLOOD PRESSURE INCREASED
6694678 CARDIAC FAILURE CHRONIC
6694678 DECREASED APPETITE
6694678 HALLUCINATION
6694678 PARANOIA
6694678 TACHYCARDIA
6694678 WEIGHT DECREASED

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

Event ID RPSR COD
6694678 FGN
6694678 HP
6694678 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6694678 1013559175 20080331 20090420 384 DAY