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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86149272 | 8614927 | 2 | F | 20160602 | 20120614 | 20160818 | PER | US-ASTRAZENECA-2012SE37392 | ASTRAZENECA | 50.00 | YR | F | Y | 0.00000 | 20160818 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86149272 | 8614927 | 1 | PS | SEROQUEL XR | QUETIAPINE FUMARATE | 1 | Oral | 400.0MG UNKNOWN | 22047 | 400 | MG | PROLONGED-RELEASE TABLET | |||||||
| 86149272 | 8614927 | 2 | SS | SEROQUEL XR | QUETIAPINE FUMARATE | 1 | Oral | UNKNOWN | 22047 | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 86149272 | 8614927 | Adverse event | |
| 86149272 | 8614927 | Anxiety | |
| 86149272 | 8614927 | Drug dose omission | |
| 86149272 | 8614927 | Feeling abnormal | |
| 86149272 | 8614927 | Panic attack |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |