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
125023442 12502344 2 F 20160329 20160704 20160627 20160708 EXP AU-ABBVIE-16P-008-1658642-00 ABBVIE 59.05 YR M Y 78.60000 KG 20160708 OT COUNTRY NOT SPECIFIED 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
125023442 12502344 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 3 IN THE MORNING, 1 AT NIGHT; THERAPY COMPLETED UNKNOWN 206619 TABLET
125023442 12502344 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral THERAPY COMPLETED UNKNOWN 0 600 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125023442 12502344 1 Hepatitis C
125023442 12502344 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125023442 12502344 LT
125023442 12502344 HO
125023442 12502344 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125023442 12502344 Abdominal pain upper
125023442 12502344 Cholelithiasis
125023442 12502344 Gastritis
125023442 12502344 Hiatus hernia
125023442 12502344 Hydronephrosis
125023442 12502344 Hypertension
125023442 12502344 Inguinal hernia
125023442 12502344 Oesophageal adenocarcinoma
125023442 12502344 Pancreatitis
125023442 12502344 Splenomegaly
125023442 12502344 Varices oesophageal
125023442 12502344 Vomiting

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
125023442 12502344 1 20150925 20160311 0
125023442 12502344 2 20150925 20160311 0