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
6202953 7008382 I 6202953-8 20080925 20090507 20090519 EXP 2009AP001863 APOTEX INC. F N 20090518 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
6202953 1011628956 PS MYCOPHENOLATE MOFETIL 1 750 MG;BID ; 250 MG;QID D 90419
6202953 1011660230 SS ARANESP 1 SUBCUTANEOUS 20 UG;SC;QW ; 20 UG;SC;QW ; 40 UG;SC;QW ; 60 UG;SC;QW U D
6202953 1011660232 SS EPREX 1 INTRAVENOUS 12000 IU;QW ; 10000 IU;IV;QW D D
6202953 1011660236 SS TACROLIMUS 1 3.5 MG;BID ; 2.5 MG;BID ; 3.5 MG;QD ; 3.5 MG;BID ; 3 MG;QD D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6202953 1011628956 DRUG USE FOR UNKNOWN INDICATION
6202953 1011660230 NEPHROGENIC ANAEMIA
6202953 1011660232 NEPHROGENIC ANAEMIA
6202953 1011660236 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6202953 HO
6202953 OT

Reactions reported

Event ID PT
6202953 APLASIA PURE RED CELL
6202953 BONE MARROW FAILURE
6202953 DRUG INEFFECTIVE
6202953 DRUG SPECIFIC ANTIBODY ABSENT
6202953 RENAL TRANSPLANT

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

Event ID RPSR COD
6202953 HP
6202953 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6202953 1011628956 20080919
6202953 1011660230 20060601 20070826
6202953 1011660230 20081012 20081109
6202953 1011660230 20081110 20081123
6202953 1011660230 20081124 20081201
6202953 1011660232 20080314 20080917
6202953 1011660232 20080207
6202953 1011660236 20080919