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
125646093 12564609 3 F 20160613 20160907 20160718 20160908 EXP US-ROCHE-1794193 ROCHE 64.15 YR M Y 79.50000 KG 20160908 OT 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
125646093 12564609 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 0.125ML/45MG FOR TWO WEEKS THEN 0.25ML/90 MG AND THEN 0.5ML/180MG U 103964 180 UG /wk
125646093 12564609 2 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 0 QD
125646093 12564609 3 C BABY ASPIRIN ASPIRIN 1 0
125646093 12564609 4 C CIALIS TADALAFIL 1 Oral AS REQUIRED 0 5 MG
125646093 12564609 5 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 Oral AS REQUIRED 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125646093 12564609 1 Essential thrombocythaemia

Outcome of event

Event ID CASEID OUTC COD
125646093 12564609 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125646093 12564609 Discomfort
125646093 12564609 Headache
125646093 12564609 Myalgia
125646093 12564609 Neutropenia
125646093 12564609 Pain
125646093 12564609 Splenomegaly
125646093 12564609 Tenderness
125646093 12564609 White blood cell count decreased

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
125646093 12564609 1 20160607 20160719 0
125646093 12564609 2 20130322 0
125646093 12564609 4 20151230 0