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
126782701 12678270 1 I 20151209 20151210 20160823 20160823 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-087119 BRISTOL MYERS SQUIBB 51.65 YR M Y 110.60000 KG 20160823 OT 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
126782701 12678270 1 PS NIVOLUMAB NIVOLUMAB 1 Intravenous (not otherwise specified) 3 MG/KG, Q2WK Y 125554 3 MG/KG SOLUTION FOR INJECTION QOW
126782701 12678270 2 SS TEMOZOLOMIDE. TEMOZOLOMIDE 1 Oral 170 MG, UNK Y 0 170 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126782701 12678270 1 Glioblastoma
126782701 12678270 2 Glioblastoma

Outcome of event

Event ID CASEID OUTC COD
126782701 12678270 HO
126782701 12678270 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126782701 12678270 Anaemia
126782701 12678270 Febrile neutropenia
126782701 12678270 Gastrointestinal haemorrhage
126782701 12678270 Gastrointestinal pain
126782701 12678270 Leukopenia
126782701 12678270 Neutropenia
126782701 12678270 Thrombocytopenia

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
126782701 12678270 1 20151028 0
126782701 12678270 2 20151104 0