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
127879101 12787910 1 I 20151105 0 20160928 20160928 DIR FDA-CTU 1.26 YR F N 8.18000 KG 20160927 N 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
127879101 12787910 1 PS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 30 MG
127879101 12787910 2 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 400 MG
127879101 12787910 3 SS IFOSFAMIDE. IFOSFAMIDE 1 0 7200 MG
127879101 12787910 4 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 .8 MG
127879101 12787910 5 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 480 MG

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127879101 12787910 Hepatic atrophy
127879101 12787910 Hepatic congestion
127879101 12787910 Hepatic fibrosis
127879101 12787910 Hepatic lesion
127879101 12787910 Pyrexia

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

Event ID CASEID RPSR COD
127879101 12787910 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127879101 12787910 1 20151003 0
127879101 12787910 2 20151023 0
127879101 12787910 3 20151023 0
127879101 12787910 4 20151002 0
127879101 12787910 5 20151002 0