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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6765993 | 7061927 | F | 6765993-6 | 20100604 | 20100611 | EXP | A0787841A | GLAXOSMITHKLINE | 40 | YR | M | Y | 127.3 | KG | 20100611 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6765993 | 1013848778 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 | ||||
| 6765993 | 1013848779 | C | AVELOX | 1 | |||||||
| 6765993 | 1013848780 | C | ALBUTEROL | 1 | |||||||
| 6765993 | 1013848781 | C | ATROVENT | 1 | |||||||
| 6765993 | 1013848782 | C | INSULIN | 1 | |||||||
| 6765993 | 1013848783 | C | LOPRESSOR | 1 | |||||||
| 6765993 | 1013848784 | C | PEPCID | 1 | |||||||
| 6765993 | 1013848785 | C | VYTORIN | 1 | |||||||
| 6765993 | 1013848786 | C | KDUR | 2 | |||||||
| 6765993 | 1013848787 | C | ZESTRIL | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6765993 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6765993 | ACUTE CORONARY SYNDROME |
| 6765993 | CARDIAC DISORDER |
| 6765993 | DYSPNOEA |
| 6765993 | HYPOAESTHESIA |
| 6765993 | MYOCARDIAL INFARCTION |
| 6765993 | PARAESTHESIA |
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 |
|---|---|---|---|---|---|
| 6765993 | 1013848778 | 20060321 | 20070817 | 515 | DAY |