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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118546372 | 11854637 | 2 | F | 20000101 | 20160826 | 20151221 | 20160826 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-2001SUS0137 | BRISTOL MYERS SQUIBB | -0.97 | YR | M | Y | 0.00000 | 20160826 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118546372 | 11854637 | 1 | PS | SUSTIVA | EFAVIRENZ | 1 | Transplacental | 600 MG, QD | U | 20972 | 600 | MG | QD | ||||||
| 118546372 | 11854637 | 2 | SS | ZERIT | STAVUDINE | 1 | Transplacental | UNK | U | 0 | |||||||||
| 118546372 | 11854637 | 3 | SS | DIDANOSINE. | DIDANOSINE | 1 | Transplacental | UNK | U | 0 | |||||||||
| 118546372 | 11854637 | 4 | SS | EPIVIR | LAMIVUDINE | 1 | Transplacental | 300 MG, QD | U | 0 | 300 | MG | QD | ||||||
| 118546372 | 11854637 | 5 | SS | ZIDOVUDINE. | ZIDOVUDINE | 1 | Oral | UNK | U | 0 | |||||||||
| 118546372 | 11854637 | 6 | SS | NELFINAVIR | NELFINAVIR | 1 | Transplacental | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118546372 | 11854637 | 1 | Product used for unknown indication |
| 118546372 | 11854637 | 2 | Product used for unknown indication |
| 118546372 | 11854637 | 3 | Product used for unknown indication |
| 118546372 | 11854637 | 4 | Product used for unknown indication |
| 118546372 | 11854637 | 5 | Product used for unknown indication |
| 118546372 | 11854637 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118546372 | 11854637 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118546372 | 11854637 | Foetal exposure during pregnancy | |
| 118546372 | 11854637 | Pericarditis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 118546372 | 11854637 | 1 | 20000511 | 0 | ||
| 118546372 | 11854637 | 2 | 19970902 | 0 | ||
| 118546372 | 11854637 | 3 | 200012 | 0 | ||
| 118546372 | 11854637 | 4 | 19960814 | 0 | ||
| 118546372 | 11854637 | 5 | 200012 | 0 |