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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125868851 | 12586885 | 1 | I | 19970107 | 20160712 | 20160725 | 20160725 | EXP | GB-TEVA-676943ACC | TEVA | 33.00 | YR | M | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125868851 | 12586885 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | Unknown | 20 MILLIGRAM DAILY; 20 MG, QD | 26919.1666 | MG | U | U | 76618 | 20 | MG | TABLET | QD | ||
| 125868851 | 12586885 | 2 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | 40 MILLIGRAM DAILY; 20 MG, BID | 26919.1666 | MG | U | U | 76618 | 20 | MG | TABLET | BID | ||
| 125868851 | 12586885 | 3 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | UNK | 26919.1666 | MG | U | U | 76618 | TABLET | |||||
| 125868851 | 12586885 | 4 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | U | 0 | TABLET | ||||||||||
| 125868851 | 12586885 | 5 | C | BENDROFLUMETHIAZIDE | BENDROFLUMETHIAZIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 125868851 | 12586885 | 6 | C | PERINDOPRIL | PERINDOPRIL | 1 | UNK | 0 | |||||||||||
| 125868851 | 12586885 | 7 | C | PRAVASTATIN. | PRAVASTATIN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125868851 | 12586885 | 1 | Product used for unknown indication |
| 125868851 | 12586885 | 2 | Product used for unknown indication |
| 125868851 | 12586885 | 4 | Product used for unknown indication |
| 125868851 | 12586885 | 5 | Product used for unknown indication |
| 125868851 | 12586885 | 6 | Product used for unknown indication |
| 125868851 | 12586885 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125868851 | 12586885 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125868851 | 12586885 | Aggression | |
| 125868851 | 12586885 | Anxiety | |
| 125868851 | 12586885 | Chest discomfort | |
| 125868851 | 12586885 | Decreased interest | |
| 125868851 | 12586885 | Depressed mood | |
| 125868851 | 12586885 | Depression | |
| 125868851 | 12586885 | Disturbance in attention | |
| 125868851 | 12586885 | Dizziness | |
| 125868851 | 12586885 | Drug withdrawal syndrome | |
| 125868851 | 12586885 | Epigastric discomfort | |
| 125868851 | 12586885 | Irritability | |
| 125868851 | 12586885 | Memory impairment | |
| 125868851 | 12586885 | Muscle twitching | |
| 125868851 | 12586885 | Palpitations | |
| 125868851 | 12586885 | Panic attack | |
| 125868851 | 12586885 | Paranoia | |
| 125868851 | 12586885 | Pruritus | |
| 125868851 | 12586885 | Psychiatric symptom | |
| 125868851 | 12586885 | Respiratory rate increased | |
| 125868851 | 12586885 | Sexual dysfunction | |
| 125868851 | 12586885 | Suicidal ideation | |
| 125868851 | 12586885 | Tearfulness | |
| 125868851 | 12586885 | Tension |
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 |
|---|---|---|---|---|---|---|
| 125868851 | 12586885 | 1 | 20000914 | 20160526 | 0 | |
| 125868851 | 12586885 | 2 | 19990401 | 20000816 | 0 | |
| 125868851 | 12586885 | 3 | 19961223 | 0 |