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
123070182 12307018 2 F 20151207 20160707 20160426 20160712 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-030916 BRISTOL MYERS SQUIBB 52.42 YR F Y 0.00000 20160712 PH 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
123070182 12307018 1 PS DAKLINZA DACLATASVIR 1 Oral 1 TAB, QD U 5H71963C 206843 1 DF FILM-COATED TABLET QD
123070182 12307018 2 SS SOVALDI SOFOSBUVIR 1 Unknown 1 TAB, QD 005556 0 1 DF QD
123070182 12307018 3 SS RIBASPHERE RIBAVIRIN 1 Oral 1 DF, BID AB94482 0 1 DF CAPSULE BID
123070182 12307018 4 C KRILL OIL DIETARY SUPPLEMENT 1 Unknown U 0
123070182 12307018 5 C IRON IRON 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123070182 12307018 1 Hepatitis C
123070182 12307018 2 Hepatitis C
123070182 12307018 3 Hepatitis C
123070182 12307018 4 Product used for unknown indication
123070182 12307018 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123070182 12307018 Arthralgia
123070182 12307018 Fatigue
123070182 12307018 Insomnia
123070182 12307018 Migraine
123070182 12307018 Muscle spasms
123070182 12307018 Nausea
123070182 12307018 Stomatitis

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
123070182 12307018 1 20151207 0
123070182 12307018 2 20151207 0
123070182 12307018 3 20151207 0