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
5472335 6264796 F 5472335-5 20060401 20070920 20070929 EXP PHBS2007JP04334 NOVARTIS PHARMACEUTICALS CORP. 55 YR M Y 20070927 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
5472335 1008989606 SS SIMULECT 1 20 MG, ONCE/SINGLE
5472335 1008989607 SS SIMULECT 1 20 MG, ONCE/SINGLE
5472335 1008989608 PS NEORAL 1 ORAL UNK, UNK 050715
5472335 1008989609 SS CELLCEPT 1 ORAL 2 G/D
5472335 1008989610 SS MEDROL 1 ORAL UNK, UNK
5472335 1008989611 SS RITUXAN 1 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
5472335 1008989606 RENAL TRANSPLANT
5472335 1008989608 RENAL TRANSPLANT
5472335 1008989609 RENAL TRANSPLANT
5472335 1008989610 RENAL TRANSPLANT
5472335 1008989611 RENAL TRANSPLANT

Outcome of event

Event ID OUTC COD
5472335 HO
5472335 OT

Reactions reported

Event ID PT
5472335 ANAEMIA
5472335 CYTOMEGALOVIRUS ANTIGEN POSITIVE
5472335 DUODENAL ULCER HAEMORRHAGE
5472335 FAECES DISCOLOURED
5472335 GASTRECTOMY
5472335 PYLORECTOMY

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
5472335 1008989606 20060315 20060315 1440 MIN
5472335 1008989607 20060319 20060319 1440 MIN
5472335 1008989608 20060314
5472335 1008989609 20060215
5472335 1008989610 20060215
5472335 1008989611 20060215