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
5117570 6135339 F 5117570-0 20060905 20060914 20060929 EXP US-ROCHE-463802 ROCHE 68 YR F Y 59.5 KG 20060929 MD UNITED STATES

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
5117570 1007716875 PS CAPECITABINE 2 ORAL 20896
5117570 1007716876 SS AVASTIN 1 INTRAVENOUS 020896
5117570 1007716877 C OXYCODONE HCL 1
5117570 1007716878 C DEXAMETHASONE TAB 1
5117570 1007716879 C DULCOLAX 1
5117570 1007716880 C REGLAN 1
5117570 1007716881 C AMBIEN 1
5117570 1007716882 C PROTONIX 1
5117570 1007716883 C SENOKOT 1
5117570 1007716884 C OXYCONTIN 1
5117570 1007716885 C CORGARD 1
5117570 1007716886 C DIGOXIN 1
5117570 1007716887 C LASIX 1
5117570 1007716888 C GLIPIZIDE 1
5117570 1007716889 C ACTIGALL 1
5117570 1007716890 C CENTRUM 2
5117570 1007716891 C PRILOSEC 1
5117570 1007716892 C DIOVAN 1
5117570 1007716893 C NORVASC 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117570 1007716875 BREAST CANCER
5117570 1007716876 BREAST CANCER

Outcome of event

Event ID OUTC COD
5117570 HO

Reactions reported

Event ID PT
5117570 PERIRECTAL ABSCESS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5117570 1007716875 20060117
5117570 1007716876 20060117