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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124594913 | 12459491 | 3 | F | 20160525 | 20160810 | 20160613 | 20160812 | EXP | US-GLAXOSMITHKLINE-US2016083424 | GLAXOSMITHKLINE | 93.00 | YR | F | Y | 0.00000 | 20160812 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124594913 | 12459491 | 1 | PS | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | W4040 | 22122 | GEL | |||||||||
124594913 | 12459491 | 2 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | UNK | U | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124594913 | 12459491 | 1 | Arthritis |
124594913 | 12459491 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124594913 | 12459491 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124594913 | 12459491 | Arthralgia | |
124594913 | 12459491 | Drug administered at inappropriate site | |
124594913 | 12459491 | Drug ineffective for unapproved indication | |
124594913 | 12459491 | Fall |
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 |
---|---|---|---|---|---|---|
124594913 | 12459491 | 1 | 20160525 | 0 |