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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
73265815 | 7326581 | 5 | F | 20160908 | 20100321 | 20160909 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-15024797 | BRISTOL MYERS SQUIBB | 0.00 | Y | 0.00000 | 20160909 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
73265815 | 7326581 | 1 | PS | SUSTIVA | EFAVIRENZ | 1 | Transplacental | UNK | U | 20972 | CAPSULE | ||||||||
73265815 | 7326581 | 2 | SS | TENOFOVIR DISOPROXIL FUMARATE. | TENOFOVIR DISOPROXIL FUMARATE | 1 | Transplacental | UNK | U | 0 | |||||||||
73265815 | 7326581 | 3 | SS | EMTRICITABINE | EMTRICITABINE | 1 | Transplacental | UNK | U | 0 | |||||||||
73265815 | 7326581 | 4 | SS | ABACAVIR. | ABACAVIR | 1 | Transplacental | UNK | U | 0 | |||||||||
73265815 | 7326581 | 5 | SS | LAMIVUDINE. | LAMIVUDINE | 1 | Transplacental | UNK | U | 0 | |||||||||
73265815 | 7326581 | 6 | SS | ZIDOVUDINE. | ZIDOVUDINE | 1 | Transplacental | UNK | U | 0 | |||||||||
73265815 | 7326581 | 7 | SS | NELFINAVIR | NELFINAVIR | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
73265815 | 7326581 | 1 | Product used for unknown indication |
73265815 | 7326581 | 2 | Product used for unknown indication |
73265815 | 7326581 | 3 | Product used for unknown indication |
73265815 | 7326581 | 4 | Product used for unknown indication |
73265815 | 7326581 | 5 | Product used for unknown indication |
73265815 | 7326581 | 6 | Product used for unknown indication |
73265815 | 7326581 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
73265815 | 7326581 | OT |
73265815 | 7326581 | CA |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
73265815 | 7326581 | Foetal exposure during pregnancy | |
73265815 | 7326581 | Gastroschisis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |