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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7584792 | 7996552 | F | 7584792-9 | 20101201 | 20110617 | 20110630 | EXP | PHHY2011AU51860 | NOVARTIS PHARMACEUTICAL CORPORATION | 82 | YR | M | Y | 20110630 | MD | AUSTRALIA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7584792 | 1016909639 | PS | EXELON | 1 | TRANSDERMAL | 9.5/24 HR MG | 022083 | ||||
7584792 | 1016909640 | C | LERCANIDIPINE | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7584792 | 1016909639 | DEMENTIA |
Outcome of event
Event ID | OUTC COD |
---|---|
7584792 | HO |
Reactions reported
Event ID | PT |
---|---|
7584792 | HICCUPS |
7584792 | SNEEZING |
7584792 | GASTROOESOPHAGEAL REFLUX DISEASE |
7584792 | ABDOMINAL PAIN UPPER |
7584792 | OESOPHAGEAL OBSTRUCTION |
7584792 | COUGH |
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 |
---|---|---|---|---|---|
7584792 | 1016909639 | 20091001 |