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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331042 | 4121251 | I | 4331042-2 | 20030101 | 20040323 | 20040331 | EXP | 2004UW05824 | ASTRAZENECA PHARMACEUTICALS | 28 | YR | M | N | 190 | LBS | 20040330 | MD | 20030101 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331042 | 1004758738 | PS | SEROQUEL | 1 | ORAL | 800 MG DAILY PO | D | D | 20639 | ||
| 4331042 | 1004767620 | SS | SEROQUEL | 1 | ORAL | 400 MG DAILY PO | D | D |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4331042 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4331042 | DRUG TOXICITY |
| 4331042 | NEUROLEPTIC MALIGNANT SYNDROME |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4331042 | HP |
Therapies reported
| no results found |