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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
97328774 | 9732877 | 4 | F | 20150429 | 20131205 | 20160715 | EXP | CA-BRISTOL-MYERS SQUIBB COMPANY-19864677 | BRISTOL MYERS SQUIBB | 53.00 | YR | F | Y | 0.00000 | 20160715 | OT | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
97328774 | 9732877 | 1 | PS | TRIAMCINOLONE ACETONIDE. | TRIAMCINOLONE ACETONIDE | 1 | Intra-articular | 40 MG, UNK | U | 14901 | 40 | MG | SUSPENSION FOR INJECTION | ||||||
97328774 | 9732877 | 2 | I | RITONAVIR. | RITONAVIR | 1 | Unknown | 100 MG, QD | U | 0 | 100 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
97328774 | 9732877 | 1 | Musculoskeletal pain |
97328774 | 9732877 | 2 | HIV infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
97328774 | 9732877 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
97328774 | 9732877 | Cushing's syndrome | |
97328774 | 9732877 | Drug interaction |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |