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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125438742 | 12543874 | 2 | F | 20150429 | 20160711 | 20160713 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-021617 | BRISTOL MYERS SQUIBB | 60.00 | YR | M | Y | 0.00000 | 20160713 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125438742 | 12543874 | 1 | PS | TRIAMCINOLONE ACETONIDE. | TRIAMCINOLONE ACETONIDE | 1 | INTRA-BURSAL | 20 MG, UNK | U | 12041 | 20 | MG | INJECTION | ||||||
| 125438742 | 12543874 | 2 | SS | RITONAVIR. | RITONAVIR | 1 | Unknown | 100 MG, QD | Y | 0 | 100 | MG | QD | ||||||
| 125438742 | 12543874 | 3 | C | LIDOCAINE. | LIDOCAINE | 1 | INTRA-BURSAL | 20 MG, UNK | U | 0 | 20 | MG | |||||||
| 125438742 | 12543874 | 4 | C | ATAZANAVIR | ATAZANAVIR | 1 | Unknown | U | 0 | ||||||||||
| 125438742 | 12543874 | 5 | C | EMTRICITABINE W/TENOFOVIR | EMTRICITABINETENOFOVIR DISOPROXIL | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125438742 | 12543874 | 1 | Product used for unknown indication |
| 125438742 | 12543874 | 2 | Product used for unknown indication |
| 125438742 | 12543874 | 3 | Bursitis |
| 125438742 | 12543874 | 4 | Product used for unknown indication |
| 125438742 | 12543874 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125438742 | 12543874 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125438742 | 12543874 | Cushing's syndrome | |
| 125438742 | 12543874 | Drug interaction |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |