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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126207512 | 12620751 | 2 | F | 20160607 | 20160907 | 20160804 | 20160908 | EXP | FR-ROCHE-1808122 | ROCHE | 14.00 | YR | F | Y | 44.00000 | KG | 20160908 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126207512 | 12620751 | 1 | PS | VALIUM | DIAZEPAM | 1 | Oral | ADJUSTABLE DOSE: 5 MG THREE TIMES | Y | 13263 | 5 | MG | TID | ||||||
| 126207512 | 12620751 | 2 | I | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | Y | 0 | ||||||||||
| 126207512 | 12620751 | 3 | SS | RITALIN | METHYLPHENIDATE HYDROCHLORIDE | 1 | Oral | Y | 0 | 10 | MG | QD | |||||||
| 126207512 | 12620751 | 4 | I | TERCIAN | CYAMEMAZINE | 1 | Intramuscular | Y | 0 | 50 | MG | QD | |||||||
| 126207512 | 12620751 | 5 | C | ABILIFY | ARIPIPRAZOLE | 1 | Oral | TREATMENT DURATION: 5 MONTHS | 0 | 5 | MG | ||||||||
| 126207512 | 12620751 | 6 | C | TERCIAN | CYAMEMAZINE | 1 | Oral | 0 | 25 | MG | FILM-COATED TABLET | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126207512 | 12620751 | 1 | Product used for unknown indication |
| 126207512 | 12620751 | 2 | Product used for unknown indication |
| 126207512 | 12620751 | 3 | Product used for unknown indication |
| 126207512 | 12620751 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126207512 | 12620751 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126207512 | 12620751 | Acute respiratory failure | |
| 126207512 | 12620751 | Agitation | |
| 126207512 | 12620751 | Drug interaction |
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 |
|---|---|---|---|---|---|---|
| 126207512 | 12620751 | 1 | 20160607 | 0 | ||
| 126207512 | 12620751 | 2 | 201605 | 20160607 | 0 | |
| 126207512 | 12620751 | 3 | 20160607 | 20160607 | 0 | |
| 126207512 | 12620751 | 4 | 20160607 | 20160607 | 0 |