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
126557051 12655705 1 I 20151208 20160816 20160816 PER US-ROCHE-1674906 ROCHE 0.00 M Y 0.00000 20160816 MD 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
126557051 12655705 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown U 103964 180 UG
126557051 12655705 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown 2 IN AM AND 3 IN PM U 21511
126557051 12655705 3 C UNSPECIFIED MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126557051 12655705 1 Hepatitis C
126557051 12655705 2 Hepatitis C
126557051 12655705 3 Oral herpes

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126557051 12655705 Alopecia
126557051 12655705 Cough
126557051 12655705 Decreased appetite
126557051 12655705 Depression
126557051 12655705 Gastric disorder
126557051 12655705 Immunodeficiency
126557051 12655705 Influenza like illness
126557051 12655705 Insomnia
126557051 12655705 Malaise
126557051 12655705 Oral herpes
126557051 12655705 Upper respiratory tract infection

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

no results found

Therapies reported

no results found