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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6696600 | 7011111 | F | 6696600-9 | 20100420 | 20100426 | EXP | A0788259A | GLAXOSMITHKLINE | 63 | YR | F | Y | 83.2 | KG | 20100426 | PH | 20080802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6696600 | 1013567780 | PS | AVANDIA | 1 | ORAL | 021071 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6696600 | 1013567780 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6696600 | DE |
| 6696600 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6696600 | ACUTE CORONARY SYNDROME |
| 6696600 | ANGINA PECTORIS |
| 6696600 | ARRHYTHMIA |
| 6696600 | ARTERIOSCLEROSIS |
| 6696600 | CARDIAC FAILURE CONGESTIVE |
| 6696600 | CARDIOMYOPATHY |
| 6696600 | DEATH |
| 6696600 | EMOTIONAL DISORDER |
| 6696600 | FAILURE TO THRIVE |
| 6696600 | FALL |
| 6696600 | HEMIPLEGIA |
| 6696600 | HYPOPHAGIA |
| 6696600 | HYPOVOLAEMIA |
| 6696600 | INTRACARDIAC THROMBUS |
| 6696600 | MYOCARDIAL INFARCTION |
| 6696600 | PAIN |
| 6696600 | PNEUMONIA |
| 6696600 | RENAL FAILURE ACUTE |
| 6696600 | SUBARACHNOID HAEMORRHAGE |
| 6696600 | SUBDURAL HAEMATOMA |
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 |
|---|---|---|---|---|---|
| 6696600 | 1013567780 | 20030527 | 20070214 |