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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 57204043 | 5720404 | 3 | F | 20041209 | 20160826 | 20050121 | 20160826 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-12821765 | BRISTOL MYERS SQUIBB | 0.00 | DY | F | Y | 1.80000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 57204043 | 5720404 | 1 | PS | VIDEX | DIDANOSINE | 1 | Transplacental | UNK | U | 20156 | |||||||||
| 57204043 | 5720404 | 2 | SS | RETROVIR | ZIDOVUDINE | 1 | Transplacental | 12 MG, QD | U | 0 | 12 | MG | QD | ||||||
| 57204043 | 5720404 | 3 | SS | VIRACEPT | NELFINAVIR MESYLATE | 1 | Transplacental | UNK | U | 0 | |||||||||
| 57204043 | 5720404 | 4 | SS | TRANQUITAL | HERBALS | 1 | Transplacental | UNK | U | 0 | |||||||||
| 57204043 | 5720404 | 5 | SS | RETROVIR | ZIDOVUDINE | 1 | Intravenous (not otherwise specified) | 1.5 MG/KG, QID | Y | 0 | 1.5 | MG/KG | QID | ||||||
| 57204043 | 5720404 | 6 | SS | RETROVIR | ZIDOVUDINE | 1 | Intravenous (not otherwise specified) | 1.5 MG/KG, BID | Y | 0 | 1.5 | MG/KG | BID | ||||||
| 57204043 | 5720404 | 7 | SS | CLAMOXYL | AMOXICILLINCLAVULANIC ACID | 1 | Intravenous (not otherwise specified) | UNK | Y | 0 | |||||||||
| 57204043 | 5720404 | 8 | C | CLAFORAN | CEFOTAXIME SODIUM | 1 | Unknown | UNK | Y | 0 | |||||||||
| 57204043 | 5720404 | 9 | C | GENTAMICIN. | GENTAMICIN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 57204043 | 5720404 | 1 | Product used for unknown indication |
| 57204043 | 5720404 | 2 | Product used for unknown indication |
| 57204043 | 5720404 | 3 | Product used for unknown indication |
| 57204043 | 5720404 | 4 | Product used for unknown indication |
| 57204043 | 5720404 | 5 | Product used for unknown indication |
| 57204043 | 5720404 | 7 | Product used for unknown indication |
| 57204043 | 5720404 | 8 | Haemophilus test positive |
| 57204043 | 5720404 | 9 | Haemophilus test positive |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 57204043 | 5720404 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 57204043 | 5720404 | Blood bilirubin increased | |
| 57204043 | 5720404 | Blood lactic acid increased | |
| 57204043 | 5720404 | C-reactive protein increased | |
| 57204043 | 5720404 | Foetal exposure during pregnancy | |
| 57204043 | 5720404 | Haemophilus test positive | |
| 57204043 | 5720404 | Premature baby | |
| 57204043 | 5720404 | Respiratory distress | |
| 57204043 | 5720404 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 57204043 | 5720404 | 2 | 20041209 | 20041209 | 0 | |
| 57204043 | 5720404 | 3 | 20041209 | 0 | ||
| 57204043 | 5720404 | 4 | 20041209 | 0 | ||
| 57204043 | 5720404 | 5 | 20041209 | 0 | ||
| 57204043 | 5720404 | 7 | 20041209 | 20041210 | 0 | |
| 57204043 | 5720404 | 8 | 20041210 | 0 |