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
124790732 12479073 2 F 2015 20160919 20160620 20160921 EXP PL-ROCHE-1776764 ROCHE 30.00 YR M Y 0.00000 20160921 MD PL PL

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
124790732 12479073 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown U 103964
124790732 12479073 2 SS COPEGUS RIBAVIRIN 1 Unknown U 21511 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124790732 12479073 1 Antiviral treatment
124790732 12479073 2 Antiviral treatment

Outcome of event

Event ID CASEID OUTC COD
124790732 12479073 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124790732 12479073 Arthralgia
124790732 12479073 Asthenia
124790732 12479073 Back pain
124790732 12479073 Blood uric acid increased
124790732 12479073 Body temperature increased
124790732 12479073 Chills
124790732 12479073 Fatigue
124790732 12479073 Glomerular filtration rate decreased
124790732 12479073 Headache
124790732 12479073 Influenza like illness
124790732 12479073 Myalgia
124790732 12479073 Neutrophil count decreased
124790732 12479073 Platelet count decreased
124790732 12479073 Pruritus
124790732 12479073 Rash papular
124790732 12479073 Red blood cell count decreased
124790732 12479073 Somnolence
124790732 12479073 Spinal pain
124790732 12479073 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
124790732 12479073 1 20141223 201506 0
124790732 12479073 2 20141223 201506 0