The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6316541 7086585 I 6316541-6 20090810 20090814 20090820 EXP US-GENENTECH-288720 GNEFDAAERSPRD 47 M Y 20090820 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6316541 1012078056 PS RITUXIMAB 2 375 MG/M2, UNK NOT REPORTED
6316541 1012078057 SS RITUXIMAB 2 375 MG/M2, UNK NOT REPORTED
6316541 1012078058 SS IFOSFAMIDE 1 INTRAVENOUS 5000 MG/M2, UNK
6316541 1012078059 SS ETOPOSIDE 1 200 MG/M2, Q12H
6316541 1012078060 SS CARBOPLATIN 1 700 MG, UNK
6316541 1012078061 C PEGFILGRASTIM 2 6 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6316541 1012078056 B-CELL LYMPHOMA
6316541 1012078058 B-CELL LYMPHOMA
6316541 1012078059 B-CELL LYMPHOMA
6316541 1012078060 B-CELL LYMPHOMA
6316541 1012078061 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6316541 HO

Reactions reported

Event ID PT
6316541 FEBRILE NEUTROPENIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6316541 1012078056 20090501
6316541 1012078057 20090801
6316541 1012078058 20090801
6316541 1012078059 20090801
6316541 1012078060 20090801
6316541 1012078061 20090803 20090803 1 DAY