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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125657233 | 12565723 | 3 | F | 20160819 | 20160718 | 20160825 | EXP | DK-VIIV HEALTHCARE LIMITED-DK2016GSK100806 | VIIV | 50.00 | YR | F | Y | 0.00000 | 20160825 | MD | DK | DK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125657233 | 12565723 | 1 | PS | Dolutegravir | DOLUTEGRAVIR | 1 | Unknown | UNK | U | U | 204790 | ||||||||
125657233 | 12565723 | 2 | SS | COMBIVIR | LAMIVUDINEIDOVUDINE | 1 | 1 DF, BID, TABLET | U | U | 0 | 1 | DF | TABLET | BID | |||||
125657233 | 12565723 | 3 | SS | Maraviroc | MARAVIROC | 1 | 150 MG, BID | U | U | 0 | 150 | MG | TABLET | BID | |||||
125657233 | 12565723 | 4 | SS | RETROVIR | ZIDOVUDINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
125657233 | 12565723 | 5 | SS | NORVIR | RITONAVIR | 1 | Unknown | 100 MG, BID | U | 0 | 100 | MG | BID | ||||||
125657233 | 12565723 | 6 | SS | DARUNAVIR | DARUNAVIR | 1 | Unknown | 600 MG, BID | U | U | 0 | 600 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125657233 | 12565723 | 1 | Acquired immunodeficiency syndrome |
125657233 | 12565723 | 2 | Acquired immunodeficiency syndrome |
125657233 | 12565723 | 3 | Acquired immunodeficiency syndrome |
125657233 | 12565723 | 4 | Acquired immunodeficiency syndrome |
125657233 | 12565723 | 5 | Acquired immunodeficiency syndrome |
125657233 | 12565723 | 6 | Acquired immunodeficiency syndrome |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125657233 | 12565723 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125657233 | 12565723 | Anaemia | |
125657233 | 12565723 | Pathogen resistance | |
125657233 | 12565723 | Treatment noncompliance |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |