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
127559781 12755978 1 I 20160915 20160916 20160916 EXP GB-009507513-1609GBR008064 MERCK 41.00 YR M Y 0.00000 20160916 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
127559781 12755978 1 PS RALTEGRAVIR POTASSIUM RALTEGRAVIR POTASSIUM 1 Unknown 400 MG, UNK U U 22145 400 MG TABLET
127559781 12755978 2 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 300 MG, UNK U U 0 300 MG
127559781 12755978 3 SS NORVIR RITONAVIR 1 Oral 100 MG, UNK U U 0 100 MG
127559781 12755978 4 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown 800 MG, UNK U U 0 800 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127559781 12755978 1 Product used for unknown indication
127559781 12755978 2 Product used for unknown indication
127559781 12755978 3 Product used for unknown indication
127559781 12755978 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127559781 12755978 OT
127559781 12755978 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127559781 12755978 Diabetes mellitus
127559781 12755978 Skin ulcer

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

no results found

Therapies reported

no results found