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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5375199 | 6346141 | I | 5375199-3 | 20060914 | 20070629 | PER | US-ASTRAZENECA-2006UW18009 | AZPRODUW00 | F | Y | 20070629 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5375199 | 1008648569 | PS | TAMOXIFEN CITRATE | 1 | ORAL | 017970 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5375199 | OT |
Reactions reported
Event ID | PT |
---|---|
5375199 | PULMONARY THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |