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
127236842 12723684 2 F 20160830 20160928 20160908 20160930 EXP GB-JNJFOC-20160901980 JANSSEN 41.89 YR A M Y 0.00000 20160930 CN 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
127236842 12723684 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral U U UNKNOWN 21976 800 MG TABLETS
127236842 12723684 2 SS NORVIR RITONAVIR 1 Oral U UNKNOWN 0 100 MG TABLET
127236842 12723684 3 SS RALTEGRAVIR. RALTEGRAVIR 1 Oral U UNKNOWN 0 400 MG TABLET
127236842 12723684 4 SS LAMIVUDINE. LAMIVUDINE 1 Oral U UNKNOWN 0 300 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127236842 12723684 1 HIV infection
127236842 12723684 2 HIV infection
127236842 12723684 3 HIV infection
127236842 12723684 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127236842 12723684 OT
127236842 12723684 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127236842 12723684 Skin ulcer

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

no results found

Therapies reported

no results found