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
124603864 12460386 4 F 2005 20160726 20160613 20160803 EXP US-PFIZER INC-2016257789 PFIZER 17.00 YR F Y 0.00000 20160803 MD 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
124603864 12460386 1 PS RAPAMUNE SIROLIMUS 1 1 MG, 1X/DAY 21110 1 MG TABLET QD
124603864 12460386 2 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 UNK 0
124603864 12460386 3 C AMOXICILLIN. AMOXICILLIN 1 UNK 0
124603864 12460386 4 C URSODIOL. URSODIOL 1 UNK 0
124603864 12460386 5 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 UNK 0
124603864 12460386 6 C PREDNISONE. PREDNISONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124603864 12460386 1 Liver and small intestine transplant

Outcome of event

Event ID CASEID OUTC COD
124603864 12460386 HO
124603864 12460386 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124603864 12460386 Coagulopathy
124603864 12460386 Liver transplant rejection
124603864 12460386 Platelet count decreased
124603864 12460386 Product use issue

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
124603864 12460386 1 19990304 0
124603864 12460386 2 1990 0
124603864 12460386 3 1990 0
124603864 12460386 4 2014 0
124603864 12460386 5 1990 0
124603864 12460386 6 2014 2015 0