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
126020083 12602008 3 F 2013 20160923 20160728 20160928 PER US-PFIZER INC-2016325672 PFIZER 56.00 YR M Y 123.30000 KG 20160928 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
126020083 12602008 1 PS RAPAMUNE SIROLIMUS 1 1 MG, 1X/DAY 21110 1 MG TABLET QD
126020083 12602008 2 C MYFORTIC MYCOPHENOLATE SODIUM 1 Oral 360 MG, 4X/DAY 0 360 MG QID
126020083 12602008 3 C MYFORTIC MYCOPHENOLATE SODIUM 1 0
126020083 12602008 4 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral 3 DF, DAILY 0 3 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126020083 12602008 1 Liver transplant
126020083 12602008 2 Transplant rejection
126020083 12602008 3 Liver transplant
126020083 12602008 4 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126020083 12602008 Condition aggravated
126020083 12602008 Product use issue
126020083 12602008 Tremor

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
126020083 12602008 1 2005 0
126020083 12602008 2 2005 0
126020083 12602008 4 2007 0