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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6732207 | 7393097 | F | 6732207-2 | 20100511 | 20100519 | EXP | A0794858A | GLAXOSMITHKLINE | 63 | YR | F | Y | 95.5 | KG | 20100519 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6732207 | 1013714585 | PS | AVANDIA | 1 | ORAL | 8MG PER DAY | 021071 | ||||
| 6732207 | 1013714586 | SS | AVANDAMET | 1 | ORAL | 1TAB PER DAY | 021410 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6732207 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6732207 | ANXIETY |
| 6732207 | ARRHYTHMIA |
| 6732207 | ASTHENIA |
| 6732207 | BONE PAIN |
| 6732207 | CARDIAC DISORDER |
| 6732207 | DEPRESSION |
| 6732207 | DIZZINESS |
| 6732207 | DYSPNOEA |
| 6732207 | EPISTAXIS |
| 6732207 | FATIGUE |
| 6732207 | JOINT SWELLING |
| 6732207 | PAIN IN EXTREMITY |
| 6732207 | STRESS |
| 6732207 | WEIGHT INCREASED |
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 |
|---|---|---|---|---|---|
| 6732207 | 1013714585 | 19990101 | 20070601 | ||
| 6732207 | 1013714586 | 20051101 |