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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6700501 | 7023260 | F | 6700501-7 | 20100423 | 20100428 | EXP | A0790535A | GLAXOSMITHKLINE | 59 | YR | F | Y | 97.7 | KG | 20100428 | OT | 20070217 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6700501 | 1013585019 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 | ||||
6700501 | 1013585020 | C | GLUCOPHAGE | 1 | |||||||
6700501 | 1013585021 | C | XOPENEX | 1 | |||||||
6700501 | 1013585022 | C | ATENOLOL | 1 | |||||||
6700501 | 1013585023 | C | LEVOTHROID | 1 | |||||||
6700501 | 1013585024 | C | ACCUPRIL | 1 | |||||||
6700501 | 1013585025 | C | LIPITOR | 1 | |||||||
6700501 | 1013585026 | C | GLUCOTROL | 1 | |||||||
6700501 | 1013585027 | C | PAXIL | 1 | |||||||
6700501 | 1013585028 | C | NEURONTIN | 1 | |||||||
6700501 | 1013585029 | C | TOPROL-XL | 1 | |||||||
6700501 | 1013585030 | C | PRILOSEC | 1 | |||||||
6700501 | 1013585031 | C | LANTUS | 1 | |||||||
6700501 | 1013585032 | C | DUONEB | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6700501 | DE |
6700501 | HO |
Reactions reported
Event ID | PT |
---|---|
6700501 | ARRHYTHMIA |
6700501 | ATRIAL FIBRILLATION |
6700501 | CARDIAC FAILURE CONGESTIVE |
6700501 | CORONARY ARTERY OCCLUSION |
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 |
---|---|---|---|---|---|
6700501 | 1013585019 | 20020201 | 20070124 |