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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125195152 | 12519515 | 2 | F | 20160706 | 20160630 | 20160718 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-052259 | BRISTOL MYERS SQUIBB | 65.00 | YR | M | Y | 0.00000 | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125195152 | 12519515 | 1 | PS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | UNK UNK, QD | Y | 5A88084 | 21436 | QD | |||||||
| 125195152 | 12519515 | 2 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Oral | 20 MG, UNK | Y | 21436 | 20 | MG | QD | ||||||
| 125195152 | 12519515 | 3 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 15 MG, Q6WK | Y | 21436 | 15 | MG | |||||||
| 125195152 | 12519515 | 4 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 10 MG, UNK | Y | 21436 | 10 | MG | |||||||
| 125195152 | 12519515 | 5 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 5 MG, UNK | Y | 21436 | 5 | MG | |||||||
| 125195152 | 12519515 | 6 | SS | ABILIFY | ARIPIPRAZOLE | 1 | Unknown | 2 MG, UNK | Y | 21436 | 2 | MG | |||||||
| 125195152 | 12519515 | 7 | C | CELEXA | CITALOPRAM HYDROBROMIDE | 1 | Unknown | U | 0 | ||||||||||
| 125195152 | 12519515 | 8 | C | LAMICTAL | LAMOTRIGINE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125195152 | 12519515 | 1 | Major depression |
| 125195152 | 12519515 | 7 | Product used for unknown indication |
| 125195152 | 12519515 | 8 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125195152 | 12519515 | Abnormal behaviour | |
| 125195152 | 12519515 | Bruxism | |
| 125195152 | 12519515 | Headache | |
| 125195152 | 12519515 | Off label use | |
| 125195152 | 12519515 | Tardive dyskinesia | |
| 125195152 | 12519515 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 125195152 | 12519515 | 1 | 200901 | 0 | ||
| 125195152 | 12519515 | 2 | 201001 | 0 | ||
| 125195152 | 12519515 | 6 | 20160611 | 0 |