The Safety Rates Drug Report

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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
124781332 12478133 2 F 20160711 20160617 20160720 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-042676 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160720 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
124781332 12478133 1 PS DAKLINZA DACLATASVIR 1 Oral 60 MG, QD 6A888398 206843 60 MG FILM-COATED TABLET QD
124781332 12478133 2 SS SOVALDI SOFOSBUVIR 1 Unknown UNK 0
124781332 12478133 3 SS RIBASPHERE RIBAVIRIN 1 Unknown UNK 0
124781332 12478133 4 C ASPIRIN /00002701/ ASPIRIN 1 Unknown U 0
124781332 12478133 5 C MULTIVIT /07504101/ 2 Unknown U 0
124781332 12478133 6 C LOSARTAN. LOSARTAN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124781332 12478133 1 Chronic hepatitis C
124781332 12478133 2 Chronic hepatitis C
124781332 12478133 3 Chronic hepatitis C
124781332 12478133 4 Product used for unknown indication
124781332 12478133 5 Product used for unknown indication
124781332 12478133 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124781332 12478133 Fatigue
124781332 12478133 Headache

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
124781332 12478133 1 201604 0
124781332 12478133 2 201604 0
124781332 12478133 3 201604 0