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
127254121 12725412 1 I 20160831 20160906 20160908 20160908 EXP ES-ABBVIE-16P-144-1720757-00 ABBVIE 0.00 A F Y 0.00000 20160908 MD ES ES

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
127254121 12725412 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 207931 2 DF TABLET QD
127254121 12725412 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0 200 MG TABLET Q12H
127254121 12725412 3 SS DARUNAVIR DARUNAVIR 1 Unknown Y UNKNOWN 0
127254121 12725412 4 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Unknown Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127254121 12725412 1 Hepatitis C
127254121 12725412 2 Hepatitis C
127254121 12725412 3 HIV infection
127254121 12725412 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127254121 12725412 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127254121 12725412 Diarrhoea
127254121 12725412 Metabolic acidosis

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
127254121 12725412 1 201607 0
127254121 12725412 2 201607 0