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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125094062 | 12509406 | 2 | F | 20151029 | 20151029 | 20160629 | 20160913 | PER | US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-08926-2015 | RECKITT BENCKISER | 0.00 | F | Y | 0.00000 | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125094062 | 12509406 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Unknown | 600 MG, SINGLE | 600 | MG | U | 0 | 600 | MG | TABLET | ||||
| 125094062 | 12509406 | 2 | SS | MUCINEX DM | DEXTROMETHORPHAN HYDROBROMIDEGUAIFENESIN | 1 | Unknown | 600 MG, SINGLE | 600 | MG | U | 0 | 600 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125094062 | 12509406 | 1 | Product used for unknown indication |
| 125094062 | 12509406 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125094062 | 12509406 | No adverse event | |
| 125094062 | 12509406 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 125094062 | 12509406 | 1 | 20151029 | 0 | ||
| 125094062 | 12509406 | 2 | 20151029 | 0 |