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
126556821 12655682 1 I 20151007 20160816 20160816 PER US-ROCHE-1643492 ROCHE 0.00 M Y 0.00000 20160816 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
126556821 12655682 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 180/0.5 ML Y B2006B04 103964
126556821 12655682 2 SS RIBASPHERE RIBAVIRIN 1 Oral U 0 600 MG BID
126556821 12655682 3 SS SOVALDI SOFOSBUVIR 1 Oral U 0 QD
126556821 12655682 4 C ASPIRIN. ASPIRIN 1 Unknown 0
126556821 12655682 5 C ALBUTEROL. ALBUTEROL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126556821 12655682 1 Hepatitis C
126556821 12655682 2 Hepatitis C
126556821 12655682 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126556821 12655682 HO
126556821 12655682 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126556821 12655682 Chills
126556821 12655682 Dizziness
126556821 12655682 Dyspnoea
126556821 12655682 Rash

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
126556821 12655682 1 20150919 20150919 0