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
126875302 12687530 2 F 20160914 20160826 20160921 EXP GB-BAUSCH-BL-2016-020268 BAUSCH AND LOMB 62.00 YR F Y 0.00000 20160921 CN GB GB

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
126875302 12687530 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070
126875302 12687530 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown U 0
126875302 12687530 3 SS DOXORUBICIN DOXORUBICIN 1 Unknown U 0
126875302 12687530 4 SS RITUXIMAB RITUXIMAB 1 Unknown U 0
126875302 12687530 5 SS VINCRISTINE VINCRISTINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126875302 12687530 1 Non-Hodgkin's lymphoma
126875302 12687530 2 Non-Hodgkin's lymphoma
126875302 12687530 3 Non-Hodgkin's lymphoma
126875302 12687530 4 Non-Hodgkin's lymphoma
126875302 12687530 5 Non-Hodgkin's lymphoma

Outcome of event

Event ID CASEID OUTC COD
126875302 12687530 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126875302 12687530 Adverse drug reaction
126875302 12687530 Oral pain
126875302 12687530 Pyrexia
126875302 12687530 Sepsis
126875302 12687530 Transfusion
126875302 12687530 Vomiting
126875302 12687530 Weight decreased

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

no results found

Therapies reported

no results found