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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125972102 | 12597210 | 2 | F | 20160727 | 20160726 | 20160803 | EXP | GB-ABBVIE-16P-167-1685460-00 | ABBVIE | 0.00 | M | Y | 0.00000 | 20160803 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125972102 | 12597210 | 1 | PS | NORVIR | RITONAVIR | 1 | Oral | 1050520 | 20945 | TABLET | |||||||||
125972102 | 12597210 | 2 | SS | DARUNAVIR | DARUNAVIR | 1 | Oral | 0 | 800 | MG | |||||||||
125972102 | 12597210 | 3 | SS | TRUVADA | EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE | 1 | Oral | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125972102 | 12597210 | 1 | HIV infection |
125972102 | 12597210 | 2 | HIV infection |
125972102 | 12597210 | 3 | HIV infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125972102 | 12597210 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125972102 | 12597210 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |