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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6530661 | 7546906 | F | 6530661-2 | 20100101 | 20100105 | 20100108 | EXP | US-RB-000078-10 | RECKITTBENCKISER | 9 | YR | M | Y | 29.25 | KG | 20100108 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6530661 | 1012915009 | PS | MUCINEX | 1 | ORAL | TOOK 1 PACKET | 090574 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6530661 | OT |
Reactions reported
Event ID | PT |
---|---|
6530661 | EPISTAXIS |
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 |
---|---|---|---|---|---|
6530661 | 1012915009 | 20100101 |