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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800801 | 12680080 | 1 | I | 20160302 | 20160824 | 20160824 | PER | US-GLAXOSMITHKLINE-CHPA2016US003089 | GLAXOSMITHKLINE | 59.00 | YR | F | Y | 0.00000 | 20160824 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800801 | 12680080 | 1 | PS | EXCEDRIN MIGRAINE | ACETAMINOPHENASPIRINCAFFEINE | 1 | Oral | 2 DF, UNK | U | FL6540 | 20802 | 2 | DF | COATED TABLET | |||||
| 126800801 | 12680080 | 2 | SS | IBUPROFEN SANDOZ (NGX) | IBUPROFEN | 1 | Unknown | UNK | U | 0 | |||||||||
| 126800801 | 12680080 | 3 | SS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | UNK, 3D | U | 0 | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126800801 | 12680080 | 1 | Arthralgia |
| 126800801 | 12680080 | 2 | Arthritis |
| 126800801 | 12680080 | 3 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126800801 | 12680080 | Drug ineffective | |
| 126800801 | 12680080 | Product use issue | |
| 126800801 | 12680080 | Therapeutic response unexpected |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |