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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124925602 | 12492560 | 2 | F | 2014 | 20160921 | 20160623 | 20160922 | EXP | US-GLAXOSMITHKLINE-US2016088411 | GLAXOSMITHKLINE | 65.00 | YR | F | Y | 0.00000 | 20160922 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124925602 | 12492560 | 1 | PS | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | W5420 | 22122 | GEL | |||||||||
124925602 | 12492560 | 2 | SS | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | U | UNK | 22122 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124925602 | 12492560 | 1 | Arthritis |
124925602 | 12492560 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124925602 | 12492560 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124925602 | 12492560 | Drug administered at inappropriate site | |
124925602 | 12492560 | Hip arthroplasty | |
124925602 | 12492560 | Inability to afford medication | |
124925602 | 12492560 | Peptic ulcer |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |