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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124211722 | 12421172 | 2 | F | 2003 | 20160708 | 20160531 | 20160711 | EXP | US-JNJFOC-20160524855 | JANSSEN | 0.00 | A | M | Y | 0.00000 | 20160711 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124211722 | 12421172 | 1 | PS | RISPERDAL | RISPERIDONE | 1 | Unknown | U | U | UNKNOWN | 20272 | UNSPECIFIED | |||||||
| 124211722 | 12421172 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
| 124211722 | 12421172 | 3 | SS | KLONOPIN | CLONAZEPAM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 124211722 | 12421172 | 4 | C | LATUDA | LURASIDONE HYDROCHLORIDE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 124211722 | 12421172 | 5 | C | PROCHLORPERAZINE. | PROCHLORPERAZINE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 124211722 | 12421172 | 6 | C | ATIVAN | LORAZEPAM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 124211722 | 12421172 | 7 | C | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124211722 | 12421172 | 1 | Product used for unknown indication |
| 124211722 | 12421172 | 2 | Seizure |
| 124211722 | 12421172 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124211722 | 12421172 | HO |
| 124211722 | 12421172 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124211722 | 12421172 | Anxiety | |
| 124211722 | 12421172 | Drug ineffective | |
| 124211722 | 12421172 | Hospitalisation | |
| 124211722 | 12421172 | Off label use | |
| 124211722 | 12421172 | Pain | |
| 124211722 | 12421172 | Product taste abnormal | |
| 124211722 | 12421172 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |