Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527739 | 7546905 | I | 6527739-6 | 20091222 | 20091222 | 20100106 | EXP | US-RB-000008-10 | RECKITTBENCKISER | 10 | YR | F | Y | 20100106 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527739 | 1012903910 | PS | MUCINEX | 1 | ORAL | 2 TEASPOONS TWICE YESTERDAY AND ONCE TODAY | 908030 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6527739 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6527739 | AGGRESSION |
| 6527739 | HEART RATE INCREASED |
| 6527739 | HYPERHIDROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6527739 | 1012903910 | 20091221 |