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
126431922 12643192 2 F 20160908 20160811 20160912 EXP US-ROCHE-1811701 ROCHE 56.00 YR M Y 0.00000 20160912 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
126431922 12643192 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 180 UG SOLUTION FOR INJECTION
126431922 12643192 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511
126431922 12643192 3 SS SOVALDI SOFOSBUVIR 1 Unknown U 0
126431922 12643192 4 C CARVEDILOL. CARVEDILOL 1 Unknown 0
126431922 12643192 5 C FINASTERIDE. FINASTERIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126431922 12643192 1 Hepatitis C
126431922 12643192 2 Hepatitis C
126431922 12643192 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126431922 12643192 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126431922 12643192 Dizziness
126431922 12643192 Fatigue
126431922 12643192 Injection site erythema
126431922 12643192 Injection site reaction
126431922 12643192 Nausea
126431922 12643192 Prostate cancer

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found