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
126557691 12655769 1 I 20151026 20160816 20160816 PER US-ROCHE-1652528 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
126557691 12655769 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous UNKNOWN 103964 180 UG /wk
126557691 12655769 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral AS DIRECTED 21511 200 MG
126557691 12655769 3 SS SOVALDI SOFOSBUVIR 1 Oral 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126557691 12655769 1 Hepatitis C
126557691 12655769 2 Hepatitis C
126557691 12655769 3 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126557691 12655769 Abdominal pain upper
126557691 12655769 Dizziness
126557691 12655769 Nervousness
126557691 12655769 Pain
126557691 12655769 Pyrexia

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
126557691 12655769 1 20151015 0
126557691 12655769 2 20151015 0
126557691 12655769 3 20151015 0