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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5078716 | 6109952 | I | 5078716-6 | 20051224 | 20060809 | DIR | M | N | 217 | LBS | 20060613 | MD | N | Y | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5078716 | 1007572344 | PS | HALDOL | 1 | ORAL | 5 MG PO Q4 HOURS PRN FOR AGITATION [RECEIVED IN 1ST 24 HOURS OF HOSPITALIZATION THEN STOPPED] | Y | D | |||
| 5078716 | 1007590071 | C | DIPHENHYRADMINE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5078716 | 1007572344 | AGITATION |
| 5078716 | 1007572344 | BIPOLAR DISORDER |
| 5078716 | 1007572344 | MANIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5078716 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5078716 | DYSTONIA |
| 5078716 | JAW 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 |
|---|---|---|---|---|---|
| 5078716 | 1007572344 | 24 | HR |