The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
93761181 9376118 1 I 20130424 20130628 20130630 20130630 EXP ES-ROCHE-1242776 ROCHE 76.00 YR M Y 93.00000 KG 20130701 PH ES ES

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
93761181 9376118 1 PS Xeloda 1 ORAL 2000 MG EVERY 12 HOURS FOR 2 WEEKS FOLLOWED BY A 1-WEEK REST PERIOD D 20896 2000 MG FILM-COATED TABLET BID
93761181 9376118 2 C CITALOPRAM 1 UNKNOWN D 0 5 MG QD
93761181 9376118 3 C Omeprazole 1 ORAL D 0 20 MG QD
93761181 9376118 4 C ATORVASTATIN 1 ORAL D 0 40 MG QD
93761181 9376118 5 C Oxaliplatin 1 ORAL D 0 250 MG /cycle
93761181 9376118 6 C ADIRO 1 ORAL D 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93761181 9376118 1 Colon cancer
93761181 9376118 5 Colon cancer

Outcome of event

Event ID CASEID OUTC COD
93761181 9376118 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93761181 9376118 Urinary incontinence

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
93761181 9376118 1 20130422 20130426 0
93761181 9376118 5 20130422 0