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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5207883 | 6432998 | I | 5207883-6 | 20010415 | 20070102 | 20070112 | EXP | DE-PFIZER INC-2007002990 | PFIZER INC | 92 | YR | F | Y | 20070112 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5207883 | 1008040347 | PS | ZOLOFT | 1 | ORAL | DAILY DOSE:50MG | 19839 | ||||
| 5207883 | 1008040348 | SS | REMINYL | 2 | ORAL | DAILY DOSE:8MG | |||||
| 5207883 | 1008040349 | C | OXAZEPAM | 1 | ORAL | ||||||
| 5207883 | 1008040350 | C | ZYPREXA | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5207883 | 1008040348 | DEMENTIA ALZHEIMER'S TYPE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5207883 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5207883 | AGITATION |
| 5207883 | DRUG EFFECT INCREASED |
| 5207883 | SLEEP DISORDER |
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 |
|---|---|---|---|---|---|
| 5207883 | 1008040347 | 20010406 | 20010427 | ||
| 5207883 | 1008040348 | 20010409 | 20010420 |