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
127227021 12722702 1 I 20160306 20160823 20160907 20160907 EXP US-ROCHE-1827272 ROCHE 9.00 YR M Y 29.80000 KG 20160908 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
127227021 12722702 1 PS Bevacizumab BEVACIZUMAB 1 Unknown MOST RECENT DOSE: 03/AUG/2015 U 125085
127227021 12722702 2 SS Bevacizumab BEVACIZUMAB 1 Unknown ALTERED DOSE U 125085 580 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127227021 12722702 1 Medulloblastoma

Outcome of event

Event ID CASEID OUTC COD
127227021 12722702 DE
127227021 12722702 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127227021 12722702 Disease progression
127227021 12722702 Lymphocyte count decreased
127227021 12722702 Neutrophil count decreased
127227021 12722702 Platelet count decreased
127227021 12722702 White blood cell count decreased

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
127227021 12722702 1 20150420 0
127227021 12722702 2 20160306 0