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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125416371 | 12541637 | 1 | I | 2003 | 20160627 | 20160708 | 20160708 | EXP | GB-TEVA-673534ACC | TEVA | 0.00 | F | Y | 0.00000 | 20160708 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125416371 | 12541637 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | Unknown | 20 MILLIGRAM DAILY; 20 MG, QD | 17040.8333 | MG | U | 76618 | 20 | MG | TABLET | QD | |||
| 125416371 | 12541637 | 2 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | 10MG/5ML | U | U | 0 | ORAL SOLUTION | |||||||
| 125416371 | 12541637 | 3 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | 20 MILLIGRAM DAILY; 20 MG, QD | 14000 | MG | U | U | 0 | 20 | MG | TABLET | QD | |||
| 125416371 | 12541637 | 4 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Oral | 20 MILLIGRAM DAILY; 20 MG, QD | 14000 | MG | U | U | 0 | 20 | MG | TABLET | QD | ||
| 125416371 | 12541637 | 5 | C | DIAZEPAM. | DIAZEPAM | 1 | 0 | ||||||||||||
| 125416371 | 12541637 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125416371 | 12541637 | 2 | Product used for unknown indication |
| 125416371 | 12541637 | 3 | Product used for unknown indication |
| 125416371 | 12541637 | 5 | Product used for unknown indication |
| 125416371 | 12541637 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125416371 | 12541637 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125416371 | 12541637 | Abnormal behaviour | |
| 125416371 | 12541637 | Abnormal dreams | |
| 125416371 | 12541637 | Agitation | |
| 125416371 | 12541637 | Anxiety | |
| 125416371 | 12541637 | Confusional state | |
| 125416371 | 12541637 | Crying | |
| 125416371 | 12541637 | Depression | |
| 125416371 | 12541637 | Diarrhoea | |
| 125416371 | 12541637 | Feeling abnormal | |
| 125416371 | 12541637 | Hyperhidrosis | |
| 125416371 | 12541637 | Hypoaesthesia | |
| 125416371 | 12541637 | Nausea | |
| 125416371 | 12541637 | Panic attack | |
| 125416371 | 12541637 | Paraesthesia | |
| 125416371 | 12541637 | Sensory disturbance | |
| 125416371 | 12541637 | Suicidal ideation | |
| 125416371 | 12541637 | Tremor | |
| 125416371 | 12541637 | Withdrawal syndrome |
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 |
|---|---|---|---|---|---|---|
| 125416371 | 12541637 | 1 | 20000901 | 0 | ||
| 125416371 | 12541637 | 2 | 20020729 | 0 | ||
| 125416371 | 12541637 | 3 | 20010131 | 20030124 | 0 | |
| 125416371 | 12541637 | 4 | 20030124 | 0 | ||
| 125416371 | 12541637 | 5 | 20020730 | 0 | ||
| 125416371 | 12541637 | 6 | 20021030 | 0 |