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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125980671 | 12598067 | 1 | I | 20160722 | 20160727 | 20160727 | EXP | RU-VIIV HEALTHCARE LIMITED-RU2016GSK106722 | VIIV | 35.00 | YR | F | Y | 0.00000 | 20160727 | CN | RU | RU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125980671 | 12598067 | 1 | PS | KIVEXA | ABACAVIR SULFATELAMIVUDINE | 1 | Oral | U | B471 | 21652 | |||||||||
125980671 | 12598067 | 2 | SS | KALETRA | LOPINAVIRRITONAVIR | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125980671 | 12598067 | 1 | Product used for unknown indication |
125980671 | 12598067 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125980671 | 12598067 | OT |
125980671 | 12598067 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125980671 | 12598067 | Drug-induced liver injury | |
125980671 | 12598067 | Exposure during pregnancy |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |