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
125455942 12545594 2 F 20160518 20160711 20160711 20160714 EXP FR-ABBVIE-16P-056-1670384-00 ABBVIE 60.97 YR M Y 0.00000 20160714 MD FR FR

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
125455942 12545594 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral Y UNKNOWN 206619 TABLET
125455942 12545594 2 SS EXVIERA DASABUVIR 1 Oral Y UNKNOWN 206619 TABLET
125455942 12545594 3 SS COPEGUS RIBAVIRIN 1 Oral Y 0
125455942 12545594 4 C TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 0
125455942 12545594 5 C ISENTRESS RALTEGRAVIR POTASSIUM 1 0
125455942 12545594 6 C APROVEL IRBESARTAN 1 0
125455942 12545594 7 C TAHOR ATORVASTATIN CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125455942 12545594 1 Chronic hepatitis C
125455942 12545594 2 Chronic hepatitis C
125455942 12545594 3 Chronic hepatitis C
125455942 12545594 4 HIV infection
125455942 12545594 5 HIV infection
125455942 12545594 6 Hypertension
125455942 12545594 7 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
125455942 12545594 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125455942 12545594 Abdominal pain
125455942 12545594 Anaemia
125455942 12545594 Asthenia
125455942 12545594 Pruritus
125455942 12545594 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
125455942 12545594 1 20160318 20160517 0
125455942 12545594 2 20160318 20160517 0
125455942 12545594 3 20160318 20160517 0