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
4541791 5705636 I 4541791-9 20041101 20041221 20041230 EXP 200413730EU AVENTIS PHARMACEUTICALS, INC. 34 YR F Y 20041230

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
4541791 1005542999 PS FLAGYL 1 ORAL
4541791 1005543000 SS SANDIMMUNE 1 ORAL
4541791 1005543001 SS SPORANOX 1 ORAL
4541791 1005543002 SS CYTOSINE ARABINOSIDE 2
4541791 1005543003 SS MITOXANTRONE 1
4541791 1005543004 SS ETOPOSIDE 1
4541791 1005543005 C IDARUBICINE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4541791 1005542999 ENTEROCOLITIS
4541791 1005543001 BRONCHOPULMONARY ASPERGILLOSIS
4541791 1005543002 ACUTE MYELOID LEUKAEMIA
4541791 1005543003 ACUTE MYELOID LEUKAEMIA
4541791 1005543004 ACUTE MYELOID LEUKAEMIA
4541791 1005543005 ACUTE MYELOID LEUKAEMIA

Outcome of event

Event ID OUTC COD
4541791 HO

Reactions reported

Event ID PT
4541791 BRONCHOPULMONARY ASPERGILLOSIS
4541791 DIPLEGIA
4541791 DIPLOPIA
4541791 POLYNEUROPATHY
4541791 STEM CELL TRANSPLANT
4541791 VOMITING

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
4541791 1005542999 20041001 20041101
4541791 1005543000 20040601
4541791 1005543001 20040601
4541791 1005543002 20021214 20040227
4541791 1005543003 20030325
4541791 1005543004 20021214 20030115
4541791 1005543005 20021214 20030115