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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6664085 | 7341252 | I | 6664085-4 | 20100329 | 20100401 | EXP | A0852768A | GLAXOSMITHKLINE | 70 | YR | M | Y | 20100401 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6664085 | 1013430966 | PS | AVANDIA | 1 | ORAL | 2MG PER DAY | 021071 | ||||
| 6664085 | 1013430967 | SS | AVANDARYL | 1 | ORAL | 1TAB TWICE PER DAY | 021700 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6664085 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6664085 | ANGIOPATHY |
| 6664085 | ARTERIAL OCCLUSIVE DISEASE |
| 6664085 | ARTERIOSCLEROSIS |
| 6664085 | HYPERTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6664085 | 1013430966 | 20050624 | |||
| 6664085 | 1013430967 | 20071020 |