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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125811122 | 12581112 | 2 | F | 2016 | 20160826 | 20160721 | 20160901 | PER | US-GLAXOSMITHKLINE-US2016103141 | GLAXOSMITHKLINE | 88.00 | YR | F | Y | 0.00000 | 20160901 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125811122 | 12581112 | 1 | PS | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | W5601 | 22122 | GEL | |||||||||
| 125811122 | 12581112 | 2 | SS | VOLTAREN | DICLOFENAC SODIUM | 1 | 22122 | GEL |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125811122 | 12581112 | 1 | Meniscus injury |
| 125811122 | 12581112 | 2 | Arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125811122 | 12581112 | Arthralgia | |
| 125811122 | 12581112 | Bone pain | |
| 125811122 | 12581112 | Drug administered at inappropriate site | |
| 125811122 | 12581112 | Drug ineffective for unapproved indication | |
| 125811122 | 12581112 | Inappropriate schedule of drug administration | |
| 125811122 | 12581112 | Product quality issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |