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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118712893 | 11871289 | 3 | F | 20151209 | 20151228 | 20151228 | 20160720 | EXP | IT-MINISAL02-338628 | IT-MYLANLABS-2015M1045776 | MYLAN | 0.00 | Y | 0.00000 | 20160719 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118712893 | 11871289 | 1 | PS | QUETIAPINE. | QUETIAPINE | 1 | Oral | 100 UNK, UNK | Y | U | 90323 | 100 | MG | QD | |||||
| 118712893 | 11871289 | 2 | C | PORTOLAC | LACTITOL | 1 | Oral | 20 ML, UNK | 0 | 20 | ML | SYRUP |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118712893 | 11871289 | 1 | Dementia Alzheimer's type |
| 118712893 | 11871289 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118712893 | 11871289 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118712893 | 11871289 | Off label use | |
| 118712893 | 11871289 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 118712893 | 11871289 | 1 | 2012 | 0 |