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
126278701 12627870 1 I 2015 20160210 20160806 20160806 PER PR-ABBVIE-16P-131-1591493-00 ABBVIE 60.00 YR M Y 0.00000 20160805 MD PR PR

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
126278701 12627870 1 PS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Oral UNKNOWN 206619 TABLET
126278701 12627870 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNKNOWN 0 TABLET
126278701 12627870 3 C TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 0
126278701 12627870 4 C RALTEGRAVIR. RALTEGRAVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126278701 12627870 1 Hepatitis C
126278701 12627870 2 Hepatitis C
126278701 12627870 3 HIV infection
126278701 12627870 4 HIV infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126278701 12627870 Depression
126278701 12627870 Drug prescribing error
126278701 12627870 Haemoglobin decreased
126278701 12627870 Hepatitis C

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
126278701 12627870 1 201508 20151114 0
126278701 12627870 2 201508 20151114 0