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
125559761 12555976 1 I 20160707 20160714 20160714 EXP US-ABBVIE-16P-163-1674530-00 ABBVIE 0.00 F Y 0.00000 20160714 MD 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
125559761 12555976 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619 TABLET
125559761 12555976 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125559761 12555976 1 Hepatitis C
125559761 12555976 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125559761 12555976 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125559761 12555976 Abdominal pain lower
125559761 12555976 Chest pain
125559761 12555976 Diarrhoea
125559761 12555976 Dry mouth
125559761 12555976 Dyspnoea
125559761 12555976 Flatulence
125559761 12555976 Hyperhidrosis

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
125559761 12555976 1 20160503 0
125559761 12555976 2 20160503 0