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
126448941 12644894 1 I 2016 20160705 20160811 20160811 PER US-ENDO PHARMACEUTICALS INC.-2016-004370 ENDO 0.00 M Y 86.26000 KG 20160811 CN US US

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
126448941 12644894 1 PS PREDNISONE TABLETS PREDNISONE 1 Unknown UNKNOWN 40256 UNKNOWN QD
126448941 12644894 2 SS VFEND VORICONAZOLE 1 Unknown 0 250 MG TABLETS Q12H
126448941 12644894 3 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown 0 500 MG TABLETS QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126448941 12644894 1 Graft versus host disease
126448941 12644894 2 Bacterial infection
126448941 12644894 3 Graft versus host disease

Outcome of event

Event ID CASEID OUTC COD
126448941 12644894 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126448941 12644894 Bacterial infection
126448941 12644894 Fluid retention
126448941 12644894 Laceration
126448941 12644894 Muscular weakness
126448941 12644894 Skin atrophy

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
126448941 12644894 1 2009 0
126448941 12644894 2 201506 0
126448941 12644894 3 2009 0