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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125103292 | 12510329 | 2 | F | 20150711 | 20150804 | 20160629 | 20160913 | PER | US-RB-079567-15 | RECKITT BENCKISER | 55.06 | YR | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125103292 | 12510329 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Unknown | 600MG. PATIENT TOOK 2 TABLETS EVERY 2-4 HOURS,FREQUENCY UNK | BG677 | 0 | 600 | MG | TABLET | ||||||
| 125103292 | 12510329 | 2 | SS | MUCINEX | GUAIFENESIN | 1 | Unknown | 600MG. PATIENT TOOK 2 TABLETS EVERY 2-4 HOURS,FREQUENCY UNK | BG677 | 0 | 600 | MG | TABLET | ||||||
| 125103292 | 12510329 | 3 | SS | MUCINEX | GUAIFENESIN | 1 | Unknown | 600MG. PATIENT TOOK 2 TABLETS EVERY 2-4 HOURS,FREQUENCY UNK | BG677 | 0 | 600 | MG | TABLET | ||||||
| 125103292 | 12510329 | 4 | C | PROMETHAZINE | PROMETHAZINEPROMETHAZINE HYDROCHLORIDE | 1 | Unknown | DOSE UNK, UNITS UNK, FREQUENCY UNK | U | 0 | |||||||||
| 125103292 | 12510329 | 5 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Unknown | DOSE UNK, UNITS UNK, FREQUENCY UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125103292 | 12510329 | 1 | Product used for unknown indication |
| 125103292 | 12510329 | 4 | Bronchitis |
| 125103292 | 12510329 | 5 | Bronchitis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125103292 | 12510329 | Inappropriate schedule of drug administration | |
| 125103292 | 12510329 | No adverse event |
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 |
|---|---|---|---|---|---|---|
| 125103292 | 12510329 | 1 | 20150711 | 0 | ||
| 125103292 | 12510329 | 2 | 20150713 | 0 | ||
| 125103292 | 12510329 | 3 | 20150723 | 0 |