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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125799512 | 12579951 | 2 | F | 20160725 | 20160721 | 20160728 | EXP | GB-VIIV HEALTHCARE LIMITED-GB2016GSK104081 | VIIV | 0.00 | F | Y | 0.00000 | 20160728 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125799512 | 12579951 | 1 | PS | KIVEXA | ABACAVIR SULFATELAMIVUDINE | 1 | Unknown | UNK | 21652 | TABLET | |||||||||
125799512 | 12579951 | 2 | SS | VIRAMUNE | NEVIRAPINE | 1 | Unknown | 400 MG, UNK | 0 | 400 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125799512 | 12579951 | 1 | HIV infection |
125799512 | 12579951 | 2 | HIV infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125799512 | 12579951 | OT |
125799512 | 12579951 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125799512 | 12579951 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |