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
90596471 9059647 1 I 20130125 0 20130206 20130206 DIR 80.00 YR M N 132.00000 LBS 20130131 OT US

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
90596471 9059647 1 PS EVEROLIMUS 1 ORAL D D 0 10 MG QD
90596471 9059647 2 SS BICALUTAMIDE 1 ORAL D D 0 50 MG QD
90596471 9059647 4 C MAALOX 1 0
90596471 9059647 5 C VIVONEX TEN 2 0
90596471 9059647 7 C GLUCOSAMINE HCL 1 0
90596471 9059647 9 C CHONDROITIN 1 0
90596471 9059647 11 C REGLAN 1 0
90596471 9059647 13 C MULTIVITAMIN 1 0
90596471 9059647 15 C PANCREATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90596471 9059647 1 Prostate cancer
90596471 9059647 2 Prostate cancer

Outcome of event

Event ID CASEID OUTC COD
90596471 9059647 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90596471 9059647 Chills
90596471 9059647 Diarrhoea
90596471 9059647 Fatigue
90596471 9059647 Hypotension
90596471 9059647 Pneumonia
90596471 9059647 Pyrexia
90596471 9059647 Urinary tract infection

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

Event ID CASEID RPSR COD
90596471 9059647 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
90596471 9059647 1 20130104 0
90596471 9059647 2 20130104 0