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
123577544 12357754 4 F 201604 20160704 20160512 20160706 EXP CA-ROCHE-1732810 ROCHE 74.32 YR F Y 0.00000 20160706 OT CA CA

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
123577544 12357754 1 PS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) N3734,N373 125085 800 MG INFUSION Q3W
123577544 12357754 2 SS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) N3734,N373 125085 400 MG Q3W
123577544 12357754 3 C NORVASC AMLODIPINE BESYLATE 1 0
123577544 12357754 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123577544 12357754 1 Ovarian cancer

Outcome of event

Event ID CASEID OUTC COD
123577544 12357754 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123577544 12357754 Balance disorder
123577544 12357754 Blood pressure increased
123577544 12357754 Ear infection
123577544 12357754 Gastrointestinal disorder
123577544 12357754 Neuropathy peripheral
123577544 12357754 Pneumonia
123577544 12357754 Rash generalised

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
123577544 12357754 1 20160307 0
123577544 12357754 2 20160518 20160628 0