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
125229032 12522903 2 F 2014 20160718 20160701 20160726 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-21575667 BRISTOL MYERS SQUIBB 0.00 M Y 69.00000 KG 20160726 CN FR FR

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
125229032 12522903 1 PS DACLATASVIR DIHYDROCHLORIDE DACLATASVIR DIHYDROCHLORIDE 1 Oral 60 MG, QD Y 206843 60 MG QD
125229032 12522903 2 SS SOFOSBUVIR SOFOSBUVIR 1 Oral 400 MG, QD Y 0 400 MG QD
125229032 12522903 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125229032 12522903 1 Chronic hepatitis C
125229032 12522903 2 Chronic hepatitis C
125229032 12522903 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125229032 12522903 HO
125229032 12522903 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125229032 12522903 Facial pain
125229032 12522903 Headache
125229032 12522903 Neck pain
125229032 12522903 Pulmonary arterial hypertension

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
125229032 12522903 1 201404 201407 0
125229032 12522903 2 201401 201407 0
125229032 12522903 3 201401 201404 0