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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118153732 | 11815373 | 2 | F | 20021025 | 20160824 | 20151209 | 20160824 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-12155131 | BRISTOL MYERS SQUIBB | 0.00 | DY | M | Y | 1.37000 | KG | 20160824 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118153732 | 11815373 | 1 | PS | EFAVIRENZ | EFAVIRENZ | 1 | Transplacental | U | 20972 | ||||||||||
| 118153732 | 11815373 | 2 | SS | VIDEX | DIDANOSINE | 1 | Transplacental | UNK | U | 0 | POWDER FOR ORAL SOLUTION | ||||||||
| 118153732 | 11815373 | 3 | C | EPIVIR | LAMIVUDINE | 1 | Transplacental | UNK | U | 0 | |||||||||
| 118153732 | 11815373 | 4 | C | KALETRA | LOPINAVIRRITONAVIR | 1 | Transplacental | UNK | U | 0 | |||||||||
| 118153732 | 11815373 | 5 | C | TRIZIVIR | ABACAVIR SULFATELAMIVUDINEIDOVUDINE | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118153732 | 11815373 | 1 | Product used for unknown indication |
| 118153732 | 11815373 | 2 | Product used for unknown indication |
| 118153732 | 11815373 | 3 | Product used for unknown indication |
| 118153732 | 11815373 | 4 | Product used for unknown indication |
| 118153732 | 11815373 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118153732 | 11815373 | CA |
| 118153732 | 11815373 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118153732 | 11815373 | Foetal exposure during pregnancy | |
| 118153732 | 11815373 | Patent ductus arteriosus | |
| 118153732 | 11815373 | Premature baby |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |