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
6669721 7352712 F 6669721-4 20100304 20100319 20100402 EXP TCI2010A00976 TAKEDA PHARMACEUTICALS NORTH AMERICA 55 YR M N 20100401 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
6669721 1013454460 PS ACTOS 1 ORAL 30 MG (30 MG, 1 IN 1 D), PER ORAL N D 21073
6669721 1013530353 C LANSORAL (LANSOPRAZOLE) 2
6669721 1013530354 C OMEPRAZOLE 1
6669721 1013530355 C PLETAL 1
6669721 1013530356 C ALLOPURINOL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6669721 1013454460 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6669721 HO

Reactions reported

Event ID PT
6669721 ABDOMINAL DISCOMFORT
6669721 DECREASED APPETITE
6669721 GASTRIC CANCER
6669721 LYMPHADENOPATHY
6669721 MALIGNANT ASCITES
6669721 METASTASES TO PERITONEUM
6669721 PYLORIC STENOSIS
6669721 REFLUX OESOPHAGITIS

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

Event ID RPSR COD
6669721 FGN
6669721 HP
6669721 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6669721 1013454460 20071022 20100305 865 DAY