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
120954176 12095417 6 F 20160207 20160802 20160219 20160805 EXP AU-ABBVIE-16P-008-1561797-00 ABBVIE 64.05 YR F Y 0.00000 20160805 MD 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
120954176 12095417 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral AV1 X2 IN MORNING, AV2 X 1, 2 TIMES A DAY U UNKNOWN 206619
120954176 12095417 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 U UNKNOWN 206619
120954176 12095417 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral U UNKNOWN 0
120954176 12095417 4 SS RIBAVIRIN. RIBAVIRIN 1 U UNKNOWN 0
120954176 12095417 5 C GLICLAZIDE GLICLAZIDE 1 0
120954176 12095417 6 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
120954176 12095417 7 C METOCLOPRAMIDE HYDROCHLORIDE. METOCLOPRAMIDE HYDROCHLORIDE 1 0
120954176 12095417 8 C PREGABALIN. PREGABALIN 1 0
120954176 12095417 9 C TEMAZEPAM. TEMAZEPAM 1 0
120954176 12095417 10 C ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 0
120954176 12095417 11 C PROPRANOLOL HYDROCHLORIDE. PROPRANOLOL HYDROCHLORIDE 1 0
120954176 12095417 12 C TEMAZEPAM. TEMAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120954176 12095417 1 Chronic hepatitis C
120954176 12095417 2 Hepatic cirrhosis
120954176 12095417 3 Chronic hepatitis C
120954176 12095417 4 Hepatic cirrhosis
120954176 12095417 5 Product used for unknown indication
120954176 12095417 6 Product used for unknown indication
120954176 12095417 7 Product used for unknown indication
120954176 12095417 8 Product used for unknown indication
120954176 12095417 9 Product used for unknown indication
120954176 12095417 10 Product used for unknown indication
120954176 12095417 11 Product used for unknown indication
120954176 12095417 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120954176 12095417 OT
120954176 12095417 HO
120954176 12095417 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
120954176 12095417 Blood bilirubin increased
120954176 12095417 Disease progression
120954176 12095417 Dizziness
120954176 12095417 Hepatic failure
120954176 12095417 Jaundice
120954176 12095417 Nausea
120954176 12095417 Sepsis

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
120954176 12095417 1 20160202 20160209 0
120954176 12095417 3 20160202 20160209 0