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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6024915 | 6870779 | I | 6024915-6 | 20081223 | 20081231 | EXP | US-PFIZER INC-2008159710 | PFIZERINC | F | Y | 20081231 | CN | 20000101 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6024915 | 1010941293 | PS | DETROL LA | 1 | 021228 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6024915 | 1010941293 | CONVULSION |
Outcome of event
Event ID | OUTC COD |
---|---|
6024915 | DE |
Reactions reported
Event ID | PT |
---|---|
6024915 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |