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
5577636 6517022 F 5577636-8 20070806 20071219 20071231 EXP PHBS2007JP13424 NOVARTIS PHARMACEUTICALS CORP. 61 YR F Y 46 KG 20071229 MD JAPAN

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
5577636 1009349349 PS GLEEVEC 1 ORAL 600 MG/D 021588
5577636 1009349350 C CYCLOPHOSPHAMIDE 1 INTRAVENOUS 800 MG/M2, UNK
5577636 1009349351 C DAUNOMYCIN 2 INTRAVENOUS 30 MG/M2, UNK
5577636 1009349352 C VINCRISTINE SULFATE 1 INTRAVENOUS 1.3 MG/M2, UNK
5577636 1009349353 C PREDNISOLONE 1 ORAL 60 MG/M2, UNK
5577636 1009349354 C MAGMITT KENEI 2 UNKNOWN 1500 MG/D
5577636 1009349355 C ZYLORIC 2 UNKNOWN 300 MG/D
5577636 1009349356 C GASTER 2 UNKNOWN 20 MG/D

Indications of drugs used

Event ID DRUG SEQ INDI PT
5577636 1009349349 ACUTE LYMPHOCYTIC LEUKAEMIA

Outcome of event

Event ID OUTC COD
5577636 OT

Reactions reported

Event ID PT
5577636 BLADDER CATHETERISATION
5577636 DYSURIA
5577636 OEDEMA
5577636 OLIGURIA
5577636 WEIGHT INCREASED

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
5577636 1009349349 20070803
5577636 1009349350 20070701
5577636 1009349351 20070701
5577636 1009349352 20070701
5577636 1009349353 20070701
5577636 1009349354 20070802
5577636 1009349355 20070724 20070830 54720 MIN
5577636 1009349356 20070724 20070823 44640 MIN