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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125622341 | 12562234 | 1 | I | 20160708 | 20160715 | 20160715 | EXP | PHHY2016BR097143 | NOVARTIS | 0.00 | M | Y | 60.00000 | KG | 20160715 | MD | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125622341 | 12562234 | 1 | PS | EXELON PATCH | RIVASTIGMINE | 1 | Transdermal | 4.6 MG, QD (5 CM2 PATCH) | U | 689210 | 22083 | 4.6 | MG | TRANS-THERAPEUTIC-SYSTEM | QD | ||||
| 125622341 | 12562234 | 2 | SS | EXELON PATCH | RIVASTIGMINE | 1 | Transdermal | 9.5 MG, QD (10CM2 PATCH) | U | 689210 | 22083 | 9.5 | MG | TRANS-THERAPEUTIC-SYSTEM | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125622341 | 12562234 | 1 | Memory impairment |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125622341 | 12562234 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125622341 | 12562234 | Condition aggravated | |
| 125622341 | 12562234 | Decreased appetite | |
| 125622341 | 12562234 | Incorrect drug administration duration | |
| 125622341 | 12562234 | Memory impairment | |
| 125622341 | 12562234 | Parkinson's disease |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |