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
126558871 12655887 1 I 20160127 20160816 20160816 PER US-ROCHE-1702448 ROCHE 0.00 F 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
126558871 12655887 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown U 103964
126558871 12655887 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126558871 12655887 1 Hepatitis C
126558871 12655887 2 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126558871 12655887 Feeling abnormal
126558871 12655887 Fibromyalgia
126558871 12655887 Pain
126558871 12655887 Pain in extremity

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

no results found

Therapies reported

no results found