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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125397751 | 12539775 | 1 | I | 20160624 | 0 | 20160707 | 20160707 | DIR | 69.00 | YR | F | N | 0.00000 | 20160706 | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125397751 | 12539775 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Oral | 3 TABLETS EVERY 12 HOURS TAKEN BY MOUTH | N | D | BX832 | 20190320 | 0 | 3 | DF | COATED TABLET | Q12H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125397751 | 12539775 | 1 | Sinus disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125397751 | 12539775 | Dizziness | |
| 125397751 | 12539775 | Dry mouth | |
| 125397751 | 12539775 | Headache | |
| 125397751 | 12539775 | Joint swelling | |
| 125397751 | 12539775 | Lip swelling | |
| 125397751 | 12539775 | Pruritus | |
| 125397751 | 12539775 | Pyrexia | |
| 125397751 | 12539775 | Rash | |
| 125397751 | 12539775 | Swelling face | |
| 125397751 | 12539775 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 125397751 | 12539775 | 1 | 20160622 | 20160623 | 0 |