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
126591762 12659176 2 F 20141106 20160822 20160817 20160825 EXP PHHO2014PL021195 NOVARTIS 75.54 YR F Y 62.00000 KG 20160825 MD 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
126591762 12659176 1 PS OFATUMUMAB OFATUMUMAB 1 Intravenous (not otherwise specified) 1000 MG, ONCE/SINGLE 125326 1000 MG 1X
126591762 12659176 2 SS ETOPOSIDE. ETOPOSIDE 1 Unknown 98 MG, UNK 0 98 MG
126591762 12659176 3 SS IFOSFAMIDE. IFOSFAMIDE 1 Unknown 1630 MG, UNK 0 1630 MG
126591762 12659176 4 SS MESNA. MESNA 1 Unknown 1324 MG, UNK 0 1324 MG
126591762 12659176 5 SS CYTARABINE. CYTARABINE 1 Unknown 815 MG, UNK 0 815 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126591762 12659176 1 Diffuse large B-cell lymphoma
126591762 12659176 2 Diffuse large B-cell lymphoma
126591762 12659176 3 Diffuse large B-cell lymphoma
126591762 12659176 4 Diffuse large B-cell lymphoma
126591762 12659176 5 Diffuse large B-cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
126591762 12659176 DS
126591762 12659176 OT
126591762 12659176 LT
126591762 12659176 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126591762 12659176 Agranulocytosis
126591762 12659176 Escherichia sepsis
126591762 12659176 Neutropenia
126591762 12659176 Pancytopenia
126591762 12659176 Pneumonia
126591762 12659176 Pyrexia

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
126591762 12659176 1 20141029 0