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
4466787 5665032 I 4466787-7 20040204 20040922 20040930 EXP TPA2004A01148 TAKEDA PHARMACEUTICALS NORTH AMERICA. 71 YR F N 170 LBS 20040929 CN

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
4466787 1005268337 PS ACTOS 1 ORAL 15 MG, 1 IN 1 D, PER ORAL D D 21073
4466787 1005290444 C CARTIA XT 1
4466787 1005290445 C PREVACID 1
4466787 1005290446 C TOPROL-XL 1
4466787 1005290447 C DIGOXIN 1
4466787 1005290449 C LISINOPRIL 1
4466787 1005290450 C WARFARIN SODIUM 1
4466787 1005290451 C GLYBURIDE 1
4466787 1005290452 C FUROSEMIDE 1
4466787 1005290453 C LIPITOR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4466787 1005268337 DIABETES MELLITUS NON-INSULIN-DEPENDENT

Outcome of event

Event ID OUTC COD
4466787 HO

Reactions reported

Event ID PT
4466787 AMNESIA
4466787 CARDIAC DISORDER
4466787 CEREBROVASCULAR ACCIDENT
4466787 ILL-DEFINED DISORDER
4466787 MYOCARDIAL INFARCTION

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

Event ID RPSR COD
4466787 CSM

Therapies reported

no results found