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
125894673 12589467 3 F 2001 20160912 20160725 20160916 EXP US-PFIZER INC-2016348927 PFIZER 58.00 YR F Y 62.00000 KG 20160916 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
125894673 12589467 1 PS RAPAMUNE SIROLIMUS 1 Oral 3 MG, DAILY (3 TABLETS OF 1 MG) 21110 3 MG TABLET
125894673 12589467 2 SS SIROLIMUS. SIROLIMUS 1 Oral 3 MG, DAILY (3 TABLETS OF 1 MG) 0 3 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125894673 12589467 1 Prophylaxis against transplant rejection
125894673 12589467 2 Prophylaxis against transplant rejection

Outcome of event

Event ID CASEID OUTC COD
125894673 12589467 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125894673 12589467 Aortic valve stenosis
125894673 12589467 Cardiac murmur
125894673 12589467 Diabetes mellitus
125894673 12589467 Diverticulitis
125894673 12589467 Pancreatitis

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
125894673 12589467 1 20010925 0
125894673 12589467 2 200109 0