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
126389421 12638942 1 I 20160801 20160809 20160809 EXP AU-BAUSCH-BL-2016-018579 BAUSCH AND LOMB 57.00 YR M Y 0.00000 20160809 OT AU AU

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
126389421 12638942 1 PS RIBAVIRIN. RIBAVIRIN 1 Unknown U 18859
126389421 12638942 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126389421 12638942 1 Product used for unknown indication
126389421 12638942 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126389421 12638942 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126389421 12638942 Decreased immune responsiveness
126389421 12638942 Drug level increased
126389421 12638942 Feeling abnormal
126389421 12638942 Gastroenteritis cryptosporidial
126389421 12638942 Headache
126389421 12638942 Insomnia
126389421 12638942 Malaise
126389421 12638942 Mouth ulceration
126389421 12638942 Nausea
126389421 12638942 Tongue ulceration

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found