Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125543831 | 12554383 | 1 | I | 2012 | 20160708 | 20160713 | 20160713 | EXP | US-GLAXOSMITHKLINE-US2016GSK098703 | GLAXOSMITHKLINE | 0.00 | M | Y | 81.63000 | KG | 20160713 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125543831 | 12554383 | 1 | PS | AVODART | DUTASTERIDE | 1 | 0.5 MG, QD | 21319 | .5 | MG | QD | ||||||||
| 125543831 | 12554383 | 2 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Oral | 200 MG, TID | 0 | 200 | MG | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125543831 | 12554383 | 1 | Nocturia |
| 125543831 | 12554383 | 2 | Epilepsy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125543831 | 12554383 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125543831 | 12554383 | Blood pressure decreased | |
| 125543831 | 12554383 | Fall | |
| 125543831 | 12554383 | Hip fracture | |
| 125543831 | 12554383 | Loss of consciousness |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125543831 | 12554383 | 1 | 2014 | 0 | ||
| 125543831 | 12554383 | 2 | 1990 | 0 |