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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4869372 | 5953260 | I | 4869372-8 | 20051201 | 20051222 | 20051230 | EXP | DE-AVENTIS-200512970DE | AVENTIS PHARMACEUTICALS, INC. | 76 | YR | M | Y | 20051230 | MD | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4869372 | 1006775824 | PS | LANTUS | 1 | 21081 | ||||||
4869372 | 1006775825 | SS | AMARYL | 1 | 020496 | ||||||
4869372 | 1006775826 | SS | CAPTOHEXAL | 2 | |||||||
4869372 | 1006775827 | SS | ASPIRIN | 1 | |||||||
4869372 | 1006775828 | C | METFORMIN | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4869372 | OT |
Reactions reported
Event ID | PT |
---|---|
4869372 | ANGIONEUROTIC OEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |