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
127735801 12773580 1 I 20160919 20160923 20160923 EXP MX-ROCHE-1832794 ROCHE 0.00 M Y 0.00000 20160923 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
127735801 12773580 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous DURING 48 WEEKS Y 103964 180 UG SOLUTION FOR INJECTION /wk
127735801 12773580 2 SS COPEGUS RIBAVIRIN 1 Unknown DURING 48 WEEKS Y 21511 TABLET
127735801 12773580 3 C DANAZOL. DANAZOL 1 Unknown 0
127735801 12773580 4 C FOLIC ACID. FOLIC ACID 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127735801 12773580 1 Hepatitis C
127735801 12773580 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127735801 12773580 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127735801 12773580 Decreased immune responsiveness
127735801 12773580 Headache
127735801 12773580 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
127735801 12773580 1 20151010 20160820 0
127735801 12773580 2 20151010 20160820 0
127735801 12773580 3 20151010 0
127735801 12773580 4 20151010 0