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
125502531 12550253 1 I 20160708 20160712 20160712 EXP GB-ABBVIE-16P-167-1672615-00 ABBVIE 0.00 M Y 0.00000 20160712 OT GB GB

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
125502531 12550253 1 PS NORVIR RITONAVIR 1 Unknown UNKNOWN 22417 100 MG TABLET
125502531 12550253 2 SS INTELENCE ETRAVIRINE 1 Unknown 0 200 MG TABLET
125502531 12550253 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown 0 800 MG
125502531 12550253 4 SS RALTEGRAVIR. RALTEGRAVIR 1 Unknown 0 400 MG
125502531 12550253 5 SS BARACLUDE ENTECAVIR 1 Unknown 0 1 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125502531 12550253 1 HIV infection
125502531 12550253 2 Product used for unknown indication
125502531 12550253 3 Product used for unknown indication
125502531 12550253 4 Product used for unknown indication
125502531 12550253 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125502531 12550253 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125502531 12550253 Death

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

no results found

Therapies reported

no results found