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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125687501 | 12568750 | 1 | I | 20160705 | 20160719 | 20160719 | EXP | CA-ALEMBIC PHARMACUETICALS LIMITED-2016SCAL000576 | ALEMBIC | 0.00 | Y | 0.00000 | 20160719 | MD | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125687501 | 12568750 | 1 | PS | DESVENLAFAXINE. | DESVENLAFAXINE | 1 | Oral | 100 MG, QD, BOTTLE OF 60 TABLETS | 204150 | 100 | MG | ||||||||
| 125687501 | 12568750 | 2 | SS | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Oral | 100 MG, QD AT BEDTIME, BOTTLE OF 60 TABLETS | 0 | 100 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125687501 | 12568750 | 1 | Depression |
| 125687501 | 12568750 | 2 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125687501 | 12568750 | HO |
| 125687501 | 12568750 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125687501 | 12568750 | Electrocardiogram QT prolonged | |
| 125687501 | 12568750 | Overdose | |
| 125687501 | 12568750 | Suicide attempt |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |