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
125306541 12530654 1 I 20160623 0 20160705 20160705 DIR 42.23 YR M N 72.40000 KG 20160624 N 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
125306541 12530654 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1500 MG
125306541 12530654 3 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 80 MG
125306541 12530654 5 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 400 MG
125306541 12530654 7 SS PREDNISONE. PREDNISONE 1 0 600 MG
125306541 12530654 9 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMRIC) RITUXIMAB 1 0 750 MG
125306541 12530654 10 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 3.2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125306541 12530654 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125306541 12530654 Febrile neutropenia
125306541 12530654 Lung infection
125306541 12530654 Respirovirus test positive
125306541 12530654 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
125306541 12530654 1 20160617 0
125306541 12530654 3 20160616 0
125306541 12530654 5 20160616 0
125306541 12530654 7 20160617 0
125306541 12530654 9 20160613 0
125306541 12530654 10 20160616 0