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
119026272 11902627 2 F 20151127 20160505 20160108 20160805 PER US-ABBVIE-15P-163-1510243-00 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
119026272 11902627 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y UNKNOWN 206619
119026272 11902627 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119026272 11902627 1 Hepatitis C
119026272 11902627 2 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119026272 11902627 Adverse drug reaction
119026272 11902627 Asthenia
119026272 11902627 Depression
119026272 11902627 Dyspnoea
119026272 11902627 Fatigue
119026272 11902627 Feeling abnormal
119026272 11902627 Haemoglobin decreased
119026272 11902627 Irritable bowel syndrome

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
119026272 11902627 1 20151113 0
119026272 11902627 2 20151113 0