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
126556581 12655658 1 I 20150901 20160816 20160816 PER US-ROCHE-1629336 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
126556581 12655658 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown Y 103964
126556581 12655658 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown Y 21511
126556581 12655658 3 SS SOVALDI SOFOSBUVIR 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126556581 12655658 1 Hepatitis C
126556581 12655658 2 Product used for unknown indication
126556581 12655658 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126556581 12655658 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126556581 12655658 Depression
126556581 12655658 Eating disorder
126556581 12655658 Fatigue
126556581 12655658 Hypophagia
126556581 12655658 Pain
126556581 12655658 Suicidal ideation

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

no results found

Therapies reported

no results found