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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7116321 | 7576379 | F | 7116321-8 | 20101115 | 20101122 | EXP | A0878947A | GLAXOSMITHKLINE | 57 | YR | F | Y | 20101122 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7116321 | 1015164260 | PS | PROMACTA | 1 | ORAL | 1TAB SINGLE DOSE | UNKNOWN | 022291 | |||
| 7116321 | 1015164261 | C | KEPPRA | 1 | |||||||
| 7116321 | 1015164262 | C | HYDROCODONE | 2 | |||||||
| 7116321 | 1015164263 | C | BENZTROPINE MESYLATE | 1 | |||||||
| 7116321 | 1015164264 | C | CALCIPOTRIENE | 1 | |||||||
| 7116321 | 1015164265 | C | CIPROFLOXACIN | 1 | |||||||
| 7116321 | 1015164266 | C | LACTULOSE | 1 | |||||||
| 7116321 | 1015164267 | C | LEVETIRACETAM | 1 | |||||||
| 7116321 | 1015164268 | C | NORFLOXACIN | 1 | |||||||
| 7116321 | 1015164269 | C | PHENYTOIN | 1 | |||||||
| 7116321 | 1015164270 | C | RISPERIDONE | 1 | |||||||
| 7116321 | 1015164271 | C | DILANTIN | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7116321 | DE |
| 7116321 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7116321 | CARDIAC ARREST |
| 7116321 | DEATH |
| 7116321 | DEPRESSED LEVEL OF CONSCIOUSNESS |
| 7116321 | GASTRIC HAEMORRHAGE |
| 7116321 | HEART RATE DECREASED |
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 |
|---|---|---|---|---|---|
| 7116321 | 1015164260 | 20100828 |