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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125109372 | 12510937 | 2 | F | 20160302 | 20160303 | 20160629 | 20160822 | PER | US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-83350-2016 | RECKITT BENCKISER | 0.00 | M | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125109372 | 12510937 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Unknown | UNK, BID, AMOUNT USED WAS FOUR CAPLETS | U | AV918 | 0 | ||||||||
| 125109372 | 12510937 | 2 | SS | MUCINEX | GUAIFENESIN | 1 | U | 0 | |||||||||||
| 125109372 | 12510937 | 3 | SS | MUCINEX | GUAIFENESIN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125109372 | 12510937 | 1 | Cough |
| 125109372 | 12510937 | 2 | Headache |
| 125109372 | 12510937 | 3 | Respiratory tract congestion |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125109372 | 12510937 | Drug ineffective | |
| 125109372 | 12510937 | Expired product administered |
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 |
|---|---|---|---|---|---|---|
| 125109372 | 12510937 | 1 | 20160302 | 0 |