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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
101908304 | 10190830 | 4 | F | 20160712 | 20140523 | 20160715 | EXP | ZA-BRISTOL-MYERS SQUIBB COMPANY-20782470 | BRISTOL MYERS SQUIBB | 1.00 | DY | F | Y | 2.17000 | KG | 20160715 | OT | ZA | ZA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
101908304 | 10190830 | 1 | PS | EFAVIRENZ | EFAVIRENZ | 1 | Transplacental | UNK | U | 21360 | FILM-COATED TABLET | ||||||||
101908304 | 10190830 | 2 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | Transplacental | UNK | U | 0 | |||||||||
101908304 | 10190830 | 3 | SS | DIACETYLMORPHINE | DIACETYLMORPHINE | 1 | Transplacental | UNK | U | 0 | |||||||||
101908304 | 10190830 | 4 | SS | METHAMPHETAMINE HCL | METHAMPHETAMINE HYDROCHLORIDE | 1 | Transplacental | UNK | U | 0 | |||||||||
101908304 | 10190830 | 5 | SS | RITONAVIR. | RITONAVIR | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
101908304 | 10190830 | 1 | Product used for unknown indication |
101908304 | 10190830 | 2 | Product used for unknown indication |
101908304 | 10190830 | 3 | Product used for unknown indication |
101908304 | 10190830 | 4 | Product used for unknown indication |
101908304 | 10190830 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
101908304 | 10190830 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
101908304 | 10190830 | Drug withdrawal syndrome neonatal | |
101908304 | 10190830 | Exposure during breast feeding | |
101908304 | 10190830 | Foetal exposure during pregnancy | |
101908304 | 10190830 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |