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
125504791 12550479 1 I 20160527 20160701 20160712 20160712 EXP PHHY2016PL093917 SANDOZ 6.00 YR F Y 20.00000 KG 20160712 CN PL PL

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
125504791 12550479 1 PS DOXORUBICIN DOXORUBICIN 1 Intravenous (not otherwise specified) 16.5 MG, QD U 200146 16.5 MG QD
125504791 12550479 2 SS TEVAGRASTIM FILGRASTIM 1 Subcutaneous 5 UG, QD 50 UG 0 5 UG QD
125504791 12550479 3 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) 2.48 G, QD 7 G U 0 2.48 G QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125504791 12550479 1 Sarcoma
125504791 12550479 2 Febrile neutropenia
125504791 12550479 3 Sarcoma

Outcome of event

Event ID CASEID OUTC COD
125504791 12550479 OT
125504791 12550479 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125504791 12550479 Anaemia
125504791 12550479 Febrile neutropenia
125504791 12550479 Haematemesis

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
125504791 12550479 1 20160524 0
125504791 12550479 2 20160505 20160514 0
125504791 12550479 3 20160524 0