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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126020251 | 12602025 | 1 | I | 20160722 | 20160728 | 20160728 | EXP | GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-060729 | BRISTOL MYERS SQUIBB | 55.00 | YR | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126020251 | 12602025 | 1 | PS | ATAZANAVIR SULFATE | ATAZANAVIR SULFATE | 1 | Unknown | 300 MG, UNK | U | U | 21567 | 300 | MG | CAPSULE, HARD | |||||
| 126020251 | 12602025 | 2 | SS | COTRIMOXAZOLE | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 126020251 | 12602025 | 3 | SS | KIVEXA | ABACAVIR SULFATELAMIVUDINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 126020251 | 12602025 | 4 | SS | NORVIR | RITONAVIR | 1 | Unknown | 100 MG, UNK | U | U | 0 | 100 | MG | ||||||
| 126020251 | 12602025 | 5 | SS | TIVICAY | DOLUTEGRAVIR SODIUM | 1 | Unknown | 50 MG, UNK | U | U | 0 | 50 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126020251 | 12602025 | 1 | Product used for unknown indication |
| 126020251 | 12602025 | 2 | Product used for unknown indication |
| 126020251 | 12602025 | 3 | Product used for unknown indication |
| 126020251 | 12602025 | 4 | Product used for unknown indication |
| 126020251 | 12602025 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126020251 | 12602025 | DE |
| 126020251 | 12602025 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126020251 | 12602025 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |