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
125836283 12583628 3 F 20150525 20160916 20160722 20160920 EXP IT-JNJFOC-20160717762 JANSSEN 66.65 YR E M Y 0.00000 20160920 PH IT IT

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
125836283 12583628 1 PS OLYSIO SIMEPREVIR 1 Oral N 205123 150 MG CAPSULE
125836283 12583628 2 SS SOVALDI SOFOSBUVIR 1 Oral 0 400 MG FILM COATED TABLET
125836283 12583628 3 SS COPEGUS RIBAVIRIN 1 Oral 0 800 MG FILM COATED TABLET
125836283 12583628 4 C ENTACT ESCITALOPRAM OXALATE 1 Oral D 0 10 MG FILM COATED TABLET
125836283 12583628 5 C IPERTEN MANIDIPINE 1 Oral D 0 20 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125836283 12583628 1 Hepatitis C
125836283 12583628 2 Hepatitis C
125836283 12583628 3 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125836283 12583628 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125836283 12583628 Dizziness
125836283 12583628 Dry skin
125836283 12583628 Hypotension
125836283 12583628 Syncope

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
125836283 12583628 1 20150415 20150708 0
125836283 12583628 2 20150415 0
125836283 12583628 3 20150415 20150708 0