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
127659781 12765978 1 I 20160830 20160915 20160921 20160921 EXP GB-GLAXOSMITHKLINE-GB2016135114 GLAXOSMITHKLINE 41.00 YR M Y 0.00000 20160921 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
127659781 12765978 1 PS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK U 20564 TABLET
127659781 12765978 2 SS NORVIR RITONAVIR 1 Unknown UNK U 0 TABLET
127659781 12765978 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown UNK, 800MG U 0 TABLET
127659781 12765978 4 SS RALTEGRAVIR POTASSIUM RALTEGRAVIR POTASSIUM 1 Oral UNK, 400 MG U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127659781 12765978 1 Product used for unknown indication
127659781 12765978 2 Product used for unknown indication
127659781 12765978 3 Product used for unknown indication
127659781 12765978 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127659781 12765978 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127659781 12765978 Skin ulcer

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

no results found

Therapies reported

no results found