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
126351701 12635170 1 I 20160730 20160802 20160808 20160808 EXP US-ABBVIE-16P-163-1692978-00 ABBVIE 65.70 YR M Y 104.42000 KG 20160808 CN COUNTRY NOT SPECIFIED 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
126351701 12635170 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y U 1047736 206619 TABLET
126351701 12635170 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y U 1047736 206619 TABLET
126351701 12635170 3 SS RIBASPHERE RIBAVIRIN 1 Oral Y 0 400 MG QD
126351701 12635170 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 0
126351701 12635170 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0
126351701 12635170 6 C LISINOPRIL. LISINOPRIL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126351701 12635170 1 Hepatitis C
126351701 12635170 3 Hepatitis C
126351701 12635170 4 Diabetes mellitus
126351701 12635170 5 Hypertension
126351701 12635170 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126351701 12635170 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126351701 12635170 Cholelithiasis
126351701 12635170 Diarrhoea
126351701 12635170 Gallbladder disorder
126351701 12635170 Nephrolithiasis

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
126351701 12635170 1 201606 20160801 0
126351701 12635170 2 20160803 0