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
127894311 12789431 1 I 20160914 20160928 20160928 EXP GB-AUROBINDO-AUR-APL-2016-11746 AUROBINDO 41.00 YR M Y 0.00000 20160928 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
127894311 12789431 1 PS LAMIVUDINE FILM-COATED TABLETS 300MG LAMIVUDINE 1 Oral 300 MG, UNK U U UNKNOWN 202032 300 MG FILM-COATED TABLET
127894311 12789431 2 SS NORVIR RITONAVIR 1 Oral 100 MG, UNK U U UNKNOWN 0 100 MG TABLET
127894311 12789431 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Oral 800 MG, UNK U U UNKNOWN 0 800 MG TABLET
127894311 12789431 4 SS RALTEGRAVIR. RALTEGRAVIR 1 Oral 400 MG, UNK U U UNKNOWN 0 400 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127894311 12789431 1 HIV infection
127894311 12789431 2 HIV infection
127894311 12789431 3 HIV infection
127894311 12789431 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127894311 12789431 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127894311 12789431 Skin ulcer

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

no results found

Therapies reported

no results found