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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119258672 | 11925867 | 2 | F | 19950328 | 20160826 | 20160119 | 20160826 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-10741387 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 0.00000 | 20160826 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119258672 | 11925867 | 1 | PS | VIDEX | DIDANOSINE | 1 | Oral | UNK | U | 20156 | |||||||||
| 119258672 | 11925867 | 2 | SS | RETROVIR | ZIDOVUDINE | 1 | Oral | UNK | U | 0 | |||||||||
| 119258672 | 11925867 | 3 | SS | BACTRIM | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119258672 | 11925867 | 1 | Antiretroviral therapy |
| 119258672 | 11925867 | 2 | Antiretroviral therapy |
| 119258672 | 11925867 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119258672 | 11925867 | OT |
| 119258672 | 11925867 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119258672 | 11925867 | Caesarean section | |
| 119258672 | 11925867 | Live birth | |
| 119258672 | 11925867 | Pre-eclampsia | |
| 119258672 | 11925867 | Pregnancy |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |