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
127338411 12733841 1 I 20141216 20160823 20160912 20160912 EXP US-ROCHE-1827840 ROCHE 19.00 YR M Y 61.40000 KG 20160912 MD US 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
127338411 12733841 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO HYPOPHOSPHATEMIA: 16/APR/2013 (COURSE 1) 125085 1840 MG SOLUTION FOR INFUSION
127338411 12733841 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO DIARRHEA: 05/AUG/2013 (COURSE 3) 125085 2441 MG SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127338411 12733841 1 Medulloblastoma

Outcome of event

Event ID CASEID OUTC COD
127338411 12733841 DE
127338411 12733841 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127338411 12733841 Death
127338411 12733841 Diarrhoea
127338411 12733841 Hypophosphataemia

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
127338411 12733841 1 20130416 0
127338411 12733841 2 20130805 20140131 0