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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127036701 | 12703670 | 1 | I | 20160604 | 20160825 | 20160831 | 20160831 | EXP | CH-JNJFOC-20160826223 | JANSSEN | 83.00 | YR | E | F | Y | 0.00000 | 20160831 | MD | CH | CH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127036701 | 12703670 | 1 | PS | DIPIPERON | PIPAMPERONE | 1 | Oral | U | U | 0 | 140 | MG | UNSPECIFIED | ||||||
| 127036701 | 12703670 | 2 | SS | HALDOL | HALOPERIDOL | 1 | Oral | 65 GTT | U | U | 0 | 6.5 | MG | DROPS |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127036701 | 12703670 | 1 | Delirium |
| 127036701 | 12703670 | 2 | Delirium |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127036701 | 12703670 | HO |
| 127036701 | 12703670 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127036701 | 12703670 | Hyperhidrosis | |
| 127036701 | 12703670 | Hypothermia | |
| 127036701 | 12703670 | Somnolence | |
| 127036701 | 12703670 | Tachycardia |
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 |
|---|---|---|---|---|---|---|
| 127036701 | 12703670 | 1 | 2016 | 0 |