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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125615041 | 12561504 | 1 | I | 201606 | 20160707 | 20160715 | 20160715 | EXP | US-GLAXOSMITHKLINE-US2016100915 | GLAXOSMITHKLINE | 59.00 | YR | M | Y | 0.00000 | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125615041 | 12561504 | 1 | PS | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK (4 AND HALF MONTHS) | U | UNK | 22122 | GEL |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125615041 | 12561504 | 1 | Limb discomfort |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125615041 | 12561504 | Abdominal discomfort | |
| 125615041 | 12561504 | Diarrhoea | |
| 125615041 | 12561504 | Hyperhidrosis | |
| 125615041 | 12561504 | Incorrect dosage administered | |
| 125615041 | 12561504 | Pyrexia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |