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
126736483 12673648 3 F 20160205 20160902 20160822 20160909 EXP JP-GILEAD-2016-0227601 GILEAD 65.00 YR E M Y 72.00000 KG 20160909 PH JP JP

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
126736483 12673648 1 PS SOVALDI SOFOSBUVIR 1 Oral 1 DF, UNK Y 204671 1 DF TABLET
126736483 12673648 2 SS SOVALDI SOFOSBUVIR 1 Unknown UNK Y 204671 TABLET
126736483 12673648 3 SS SOVALDI SOFOSBUVIR 1 Unknown 400 MG, UNK Y 204671 400 MG TABLET
126736483 12673648 4 SS REBETOL RIBAVIRIN 1 Oral 400 MG, UNK Y 0 400 MG
126736483 12673648 5 C GASTER FAMOTIDINE 1 Oral 2 DF, UNK 0 2 DF
126736483 12673648 6 C GASTER FAMOTIDINE 1 Oral 20 MG, UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126736483 12673648 1 Chronic hepatitis C
126736483 12673648 4 Chronic hepatitis C
126736483 12673648 5 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
126736483 12673648 OT
126736483 12673648 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126736483 12673648 Drug ineffective
126736483 12673648 Hepatitis C
126736483 12673648 Ileus

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
126736483 12673648 1 20151212 20160208 0
126736483 12673648 2 2016 2016 0
126736483 12673648 3 20160810 0
126736483 12673648 4 20151212 20160208 0
126736483 12673648 5 20150926 20160205 0
126736483 12673648 6 20150926 20160205 0