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
123796203 12379620 3 F 20160809 20160518 20160810 EXP US-ROCHE-1756676 ROCHE 0.00 M Y 0.00000 20160810 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
123796203 12379620 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Unknown U UNKNOWN 103964 /wk
123796203 12379620 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 U UNKNOWN 103964
123796203 12379620 3 SS COPEGUS RIBAVIRIN 1 Unknown U UNKNOWN 21511

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123796203 12379620 1 Hepatitis C
123796203 12379620 2 Hepatic cancer
123796203 12379620 3 Hepatitis

Outcome of event

Event ID CASEID OUTC COD
123796203 12379620 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123796203 12379620 Anxiety
123796203 12379620 Blood pressure decreased
123796203 12379620 Cerebrovascular accident
123796203 12379620 Crying
123796203 12379620 Hypertension
123796203 12379620 Judgement impaired
123796203 12379620 Loss of consciousness
123796203 12379620 Migraine
123796203 12379620 Product quality issue
123796203 12379620 Skin ulcer
123796203 12379620 Vomiting
123796203 12379620 Weight decreased

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
123796203 12379620 1 2010 2011 0