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
127138871 12713887 1 I 20160506 20160831 20160905 20160905 EXP MX-ROCHE-1824524 ROCHE 51.82 YR M Y 0.00000 20160905 CN MX MX

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
127138871 12713887 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 180 UG SOLUTION FOR INJECTION /wk
127138871 12713887 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 360 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127138871 12713887 1 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127138871 12713887 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127138871 12713887 Abdominal pain
127138871 12713887 Dyspnoea
127138871 12713887 Eye pain
127138871 12713887 Fatigue
127138871 12713887 Insomnia
127138871 12713887 Off label use
127138871 12713887 Pain in extremity
127138871 12713887 Product use issue

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
127138871 12713887 1 201608 0
127138871 12713887 2 20160506 20160729 0