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
4463185 4219150 F 4463185-7 20040822 20040823 20040930 EXP DE-ROCHE-378260 ROCHE 51 YR M Y 69 KG 20040930 MD

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
4463185 1005252429 PS DACLIZUMAB 2 INTRAVENOUS
4463185 1005252430 SS DACLIZUMAB 2 INTRAVENOUS
4463185 1005252431 SS DACLIZUMAB 2 INTRAVENOUS
4463185 1005252432 SS MYCOPHENOLATE MOFETIL 2 ORAL
4463185 1005252433 SS MYCOPHENOLATE MOFETIL 2 ORAL 1000 MG + 500 MG.
4463185 1005252434 SS MYCOPHENOLATE MOFETIL 2 ORAL 500 MG + 2 X 750 MG
4463185 1005252435 SS MYCOPHENOLATE MOFETIL 2 ORAL
4463185 1005252436 SS MYCOPHENOLATE MOFETIL 2 ORAL
4463185 1005252437 SS MYCOPHENOLATE MOFETIL 2 ORAL
4463185 1005252438 SS MYCOPHENOLATE MOFETIL 2 ORAL
4463185 1005252439 SS SIROLIMUS 2 ORAL
4463185 1005252440 SS SIROLIMUS 2 ORAL
4463185 1005252441 SS SIROLIMUS 2 ORAL
4463185 1005252442 SS SIROLIMUS 2 ORAL
4463185 1005252443 SS SIROLIMUS 2 ORAL
4463185 1005252444 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252445 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252446 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252447 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252448 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252449 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252450 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252451 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252452 SS PREDNISOLONE 1 INTRAVENOUS
4463185 1005252453 C ACETYLCYSTEINE 1
4463185 1005252454 C AMPHOTERICIN B 1
4463185 1005252455 C CEFUROXIM 2
4463185 1005252456 C DILTIAZEM 1
4463185 1005252457 C FUROSEMIDE 1
4463185 1005252458 C METOPROLOL 2
4463185 1005252459 C URAPIDIL 2
4463185 1005252460 C VALGANCICLOVIR 2 STOPPED ON 04 SEP 2004 AND RESTARTED ON 05 SEP 2004.

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
4463185 HO

Reactions reported

Event ID PT
4463185 ANAEMIA
4463185 ARTERIAL HAEMORRHAGE
4463185 GRAFT COMPLICATION
4463185 HYPOTENSION

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

Event ID RPSR COD
4463185 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4463185 1005252429 20040819 20040819 1
4463185 1005252430 20040902 20040902 1
4463185 1005252431 20040914 20040914 1
4463185 1005252432 20040819
4463185 1005252433 20040827 20040827 1
4463185 1005252434 20040828 20040828 1
4463185 1005252435 20040829
4463185 1005252436 20040901 20040901 1
4463185 1005252437 20040902
4463185 1005252438 20040909
4463185 1005252439 20040819 20040821 3
4463185 1005252440 20040822
4463185 1005252441 20040828
4463185 1005252442 20040904
4463185 1005252443 20040909
4463185 1005252444 20040822
4463185 1005252445 20040819 20040819 1
4463185 1005252446 20040820
4463185 1005252447 20040821
4463185 1005252448 20040823
4463185 1005252449 20040824
4463185 1005252450 20040826
4463185 1005252451 20040914
4463185 1005252452 20040920
4463185 1005252453 20040819
4463185 1005252454 20040819
4463185 1005252455 20040819
4463185 1005252456 20040819
4463185 1005252457 20040822
4463185 1005252458 20040822
4463185 1005252459 20040821 20040903 14
4463185 1005252460 20040820