The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126965351 12696535 1 I 20160725 20160825 20160830 20160830 EXP CH-SM-2016-06865 CH-ROCHE-1821344 ROCHE 58.38 YR F Y 58.00000 KG 20160830 MD CH CH

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126965351 12696535 1 PS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral 50722 500 MG BID
126965351 12696535 2 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Oral 0 5 MG QD
126965351 12696535 3 SS PREDNISON PREDNISONE 1 Oral 0 10 MG QD
126965351 12696535 4 C VALGANCICLOVIR. VALGANCICLOVIR 1 Unknown 0
126965351 12696535 5 C VALGANCICLOVIR. VALGANCICLOVIR 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126965351 12696535 1 Heart transplant
126965351 12696535 2 Heart transplant
126965351 12696535 3 Heart transplant

Outcome of event

Event ID CASEID OUTC COD
126965351 12696535 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126965351 12696535 Agranulocytosis
126965351 12696535 Cytomegalovirus colitis
126965351 12696535 Cytomegalovirus infection
126965351 12696535 Cytomegalovirus viraemia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126965351 12696535 1 201512 0
126965351 12696535 2 201512 0
126965351 12696535 3 201512 0
126965351 12696535 4 20160620 0
126965351 12696535 5 20160817 0