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
6138787 6957014 I 6138787-2 20090326 20090331 EXP PHHY2009GB11466 NOVARTIS PHARMACEUTICALS CORP. 19 YR Y 20090331 OT UNITED KINGDOM

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
6138787 1011359245 PS CYCLOSPORINE 1 050574
6138787 1011359246 SS CYCLOSPORINE 1 050574
6138787 1011359247 C CAMPATH 1 100 MG
6138787 1011359248 C BUSULPHAN 2 16 MG/KG
6138787 1011359249 C MELPHALAN 2 140 MG/M^2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6138787 1011359245 STEM CELL TRANSPLANT
6138787 1011359246 PROPHYLAXIS AGAINST GRAFT VERSUS HOST DISEASE

Outcome of event

Event ID OUTC COD
6138787 DE
6138787 HO

Reactions reported

Event ID PT
6138787 ARTERIAL HAEMORRHAGE
6138787 PNEUMONITIS
6138787 SCEDOSPORIUM INFECTION
6138787 SYSTEMIC MYCOSIS
6138787 TRACHEOSTOMY
6138787 TRACHEOSTOMY MALFUNCTION
6138787 ULCER

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

no results found

Therapies reported

no results found