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
126354431 12635443 1 I 20160710 20160803 20160808 20160808 EXP RO-ABBVIE-16P-135-1694232-00 ABBVIE 67.35 YR F Y 0.00000 20160808 CN COUNTRY NOT SPECIFIED RO

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
126354431 12635443 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 2 IN THE MORNING (2-0-0) Y UNKNOWN 206619 FILM-COATED TABLET
126354431 12635443 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Y UNKNOWN 206619
126354431 12635443 3 SS EXVIERA DASABUVIR 1 Oral 1 IN THE MORNING AND 1 IN THE EVENING (1-0-0) Y UNKNOWN 206619 FILM-COATED TABLET
126354431 12635443 4 SS EXVIERA DASABUVIR 1 Y UNKNOWN 206619
126354431 12635443 5 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0 TABLET
126354431 12635443 6 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0 TABLET BID
126354431 12635443 7 C DEXAMETHASONE. DEXAMETHASONE 1 UNKNOWN 0
126354431 12635443 8 C PREDNISONE. PREDNISONE 1 0
126354431 12635443 9 C VITAMIN C ASCORBIC ACID 1 UNKNOWN 0
126354431 12635443 10 C BETAMETHASONE. BETAMETHASONE 1 UNKNOWN 0 CREAM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126354431 12635443 1 Hepatitis C
126354431 12635443 2 Hepatic cirrhosis
126354431 12635443 3 Hepatic cirrhosis
126354431 12635443 4 Hepatitis C
126354431 12635443 5 Hepatitis C
126354431 12635443 6 Hepatic cirrhosis
126354431 12635443 7 Product used for unknown indication
126354431 12635443 8 Product used for unknown indication
126354431 12635443 9 Product used for unknown indication
126354431 12635443 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126354431 12635443 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126354431 12635443 Chest pain
126354431 12635443 Decreased appetite
126354431 12635443 Dizziness
126354431 12635443 Faeces soft
126354431 12635443 Fall
126354431 12635443 Oedema peripheral
126354431 12635443 Rash erythematous
126354431 12635443 Speech disorder
126354431 12635443 Vomiting
126354431 12635443 Weight decreased

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
126354431 12635443 1 20160710 20160801 0
126354431 12635443 3 20160710 20160801 0
126354431 12635443 5 20160710 20160726 0
126354431 12635443 7 20160715 20160725 0
126354431 12635443 8 20160726 20160801 0
126354431 12635443 9 20160715 20160725 0