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
125237771 12523777 1 I 20160630 20160704 20160704 EXP CN-ROCHE-1787504 ROCHE 0.00 M Y 0.00000 20160704 CN CN CN

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
125237771 12523777 1 PS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 Unknown 103964
125237771 12523777 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125237771 12523777 1 Hepatitis C
125237771 12523777 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125237771 12523777 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125237771 12523777 Asthenia
125237771 12523777 Haemorrhage
125237771 12523777 Insomnia
125237771 12523777 Nausea
125237771 12523777 Pain
125237771 12523777 Pyrexia

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

no results found

Therapies reported

no results found