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
126278571 12627857 1 I 20160311 20160806 20160806 PER US-ABBVIE-16P-163-1582485-00 ABBVIE 0.00 F Y 0.00000 20160805 CN 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
126278571 12627857 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 3 TABLETS IN AM: 1 TABLET IN PM U UNKNOWN 206619 TABLET
126278571 12627857 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral 3 TABLETS IN AM: 2 TABLETS IN PM U UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126278571 12627857 1 Hepatitis C
126278571 12627857 2 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126278571 12627857 Anaemia
126278571 12627857 Anxiety
126278571 12627857 Chills
126278571 12627857 Confusional state
126278571 12627857 Constipation
126278571 12627857 Depression
126278571 12627857 Diarrhoea
126278571 12627857 Fatigue
126278571 12627857 Impaired work ability
126278571 12627857 Memory impairment
126278571 12627857 Nausea
126278571 12627857 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found