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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126343961 | 12634396 | 1 | I | 1997 | 20160729 | 20160809 | 20160809 | EXP | GB-TEVA-682637ACC | TEVA | 31.00 | YR | F | Y | 0.00000 | 20160809 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126343961 | 12634396 | 1 | PS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | UNK | U | U | 76618 | TABLET | |||||||
| 126343961 | 12634396 | 2 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 20 MILLIGRAM DAILY; 20 MG, QD | U | U | 0 | 20 | MG | TABLET | QD | ||||
| 126343961 | 12634396 | 3 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 30 MILLIGRAM DAILY; 30 MG, QD | U | U | 0 | 30 | MG | TABLET | QD | ||||
| 126343961 | 12634396 | 4 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Oral | UNK | U | U | 0 | TABLET | |||||||
| 126343961 | 12634396 | 5 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Oral | 20 MILLIGRAM DAILY; 20 MG, QD, ONE EACH MORNING | U | U | 0 | 20 | MG | TABLET | QD | ||||
| 126343961 | 12634396 | 6 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Oral | 30 MILLIGRAM DAILY; 30 MG, QD, HALF TABLET | U | U | 0 | 30 | MG | TABLET | QD | ||||
| 126343961 | 12634396 | 7 | C | CLOMIPRAMINE HYDROCHLORIDE. | CLOMIPRAMINE HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126343961 | 12634396 | 1 | Perinatal depression |
| 126343961 | 12634396 | 2 | Product used for unknown indication |
| 126343961 | 12634396 | 3 | Product used for unknown indication |
| 126343961 | 12634396 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126343961 | 12634396 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126343961 | 12634396 | Amnesia | |
| 126343961 | 12634396 | Anxiety | |
| 126343961 | 12634396 | Brief psychotic disorder, with postpartum onset | |
| 126343961 | 12634396 | Bruxism | |
| 126343961 | 12634396 | Cardiac disorder | |
| 126343961 | 12634396 | Cognitive disorder | |
| 126343961 | 12634396 | Depressed mood | |
| 126343961 | 12634396 | Depression | |
| 126343961 | 12634396 | Disorientation | |
| 126343961 | 12634396 | Disturbance in attention | |
| 126343961 | 12634396 | Dizziness | |
| 126343961 | 12634396 | Drug withdrawal syndrome | |
| 126343961 | 12634396 | Fatigue | |
| 126343961 | 12634396 | Feeling of despair | |
| 126343961 | 12634396 | Insomnia | |
| 126343961 | 12634396 | Palpitations | |
| 126343961 | 12634396 | Panic attack | |
| 126343961 | 12634396 | Paraesthesia | |
| 126343961 | 12634396 | Prophylaxis | |
| 126343961 | 12634396 | Psychiatric symptom | |
| 126343961 | 12634396 | Sleep disorder | |
| 126343961 | 12634396 | Suicidal ideation | |
| 126343961 | 12634396 | Syncope | |
| 126343961 | 12634396 | Visual impairment | |
| 126343961 | 12634396 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 126343961 | 12634396 | 1 | 19960626 | 0 | ||
| 126343961 | 12634396 | 4 | 20030520 | 20030925 | 0 | |
| 126343961 | 12634396 | 7 | 19970227 | 0 |