Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4263257 | 5709722 | I | 4263257-6 | 20031224 | 20040105 | EXP | US-GLAXOSMITHKLINE-A0490813A | GLAXOSMITHKLINE | Y | 20040105 | OT |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4263257 | 1004491196 | PS | BUPROPION HCL | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4263257 | OT |
Reactions reported
Event ID | PT |
---|---|
4263257 | AORTA HYPOPLASIA |
4263257 | CONGENITAL ATRIAL SEPTAL DEFECT |
4263257 | DRUG EXPOSURE DURING PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |