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
126838052 12683805 2 F 20160901 20160825 20160908 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201608-004152 CONCORDIA 62.00 YR F Y 0.00000 20160908 OT 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
126838052 12683805 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown SECOND ROUND U U 21959
126838052 12683805 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown U U 0
126838052 12683805 3 SS DOXORUBICIN DOXORUBICIN 1 Unknown SECOND ROUND U U 0
126838052 12683805 4 SS RITUXIMAB RITUXIMAB 1 Unknown U U 0
126838052 12683805 5 SS VINCRISTINE VINCRISTINE 1 Unknown SECOND ROUND U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126838052 12683805 1 Non-Hodgkin's lymphoma
126838052 12683805 3 Non-Hodgkin's lymphoma
126838052 12683805 5 Non-Hodgkin's lymphoma

Outcome of event

Event ID CASEID OUTC COD
126838052 12683805 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126838052 12683805 Adverse drug reaction
126838052 12683805 Oral pain
126838052 12683805 Pyrexia
126838052 12683805 Sepsis
126838052 12683805 Transfusion
126838052 12683805 Vomiting
126838052 12683805 Weight decreased

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

no results found

Therapies reported

no results found