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
126418991 12641899 1 I 20130624 20150427 20160810 20160810 EXP DE-009507513-1504DEU022769 MERCK 33.00 YR M Y 0.00000 20160810 CN GB DE

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
126418991 12641899 1 PS BOCEPREVIR BOCEPREVIR 1 Oral 2400 MG, QD Y 202258 CAPSULE QD
126418991 12641899 2 SS COPEGUS RIBAVIRIN 1 Oral 1000 MG, QD Y 0 TABLET QD
126418991 12641899 3 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 180 MICROGRAM, QW 8614.132 UG Y 0 180 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126418991 12641899 1 Chronic hepatitis C
126418991 12641899 2 Chronic hepatitis C
126418991 12641899 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126418991 12641899 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126418991 12641899 Cough
126418991 12641899 Dysgeusia
126418991 12641899 Fatigue
126418991 12641899 Headache
126418991 12641899 Leukopenia

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
126418991 12641899 1 20130628 20140429 0
126418991 12641899 2 20130531 20140429 0
126418991 12641899 3 20130527 20140425 0