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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126065831 | 12606583 | 1 | I | 19951116 | 20160720 | 20160729 | 20160729 | EXP | GB-TEVA-679644ACC | TEVA | 0.00 | F | Y | 0.00000 | 20160729 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126065831 | 12606583 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | Unknown | UNK | U | U | 76618 | TABLET | |||||||
| 126065831 | 12606583 | 2 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 20 MILLIGRAM DAILY; | 16800 | MG | U | U | 76618 | 20 | MG | TABLET | QD | ||
| 126065831 | 12606583 | 3 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 30 MILLIGRAM DAILY; | 16800 | MG | U | U | 76618 | 30 | MG | TABLET | QD | ||
| 126065831 | 12606583 | 4 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 20 MG, U | U | U | 0 | 20 | MG | TABLET | |||||
| 126065831 | 12606583 | 5 | C | PROTHIADEN | DOTHIEPIN HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 126065831 | 12606583 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 126065831 | 12606583 | 7 | C | ZIMOVANE | ZOPICLONE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126065831 | 12606583 | 1 | Product used for unknown indication |
| 126065831 | 12606583 | 2 | Product used for unknown indication |
| 126065831 | 12606583 | 4 | Product used for unknown indication |
| 126065831 | 12606583 | 5 | Muscle relaxant therapy |
| 126065831 | 12606583 | 6 | Product used for unknown indication |
| 126065831 | 12606583 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126065831 | 12606583 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126065831 | 12606583 | Agitation | |
| 126065831 | 12606583 | Asthenia | |
| 126065831 | 12606583 | Bedridden | |
| 126065831 | 12606583 | Depressed mood | |
| 126065831 | 12606583 | Disorientation | |
| 126065831 | 12606583 | Dizziness | |
| 126065831 | 12606583 | Headache | |
| 126065831 | 12606583 | Incontinence | |
| 126065831 | 12606583 | Increased tendency to bruise | |
| 126065831 | 12606583 | Insomnia | |
| 126065831 | 12606583 | Malaise | |
| 126065831 | 12606583 | Mood swings | |
| 126065831 | 12606583 | Nausea | |
| 126065831 | 12606583 | Nightmare | |
| 126065831 | 12606583 | Panic attack | |
| 126065831 | 12606583 | Suicidal ideation | |
| 126065831 | 12606583 | Tearfulness | |
| 126065831 | 12606583 | Tremor | |
| 126065831 | 12606583 | Vomiting | |
| 126065831 | 12606583 | 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 |
|---|---|---|---|---|---|---|
| 126065831 | 12606583 | 1 | 19950810 | 0 | ||
| 126065831 | 12606583 | 2 | 19980305 | 19981223 | 0 | |
| 126065831 | 12606583 | 3 | 19980615 | 20011216 | 0 | |
| 126065831 | 12606583 | 4 | 19960328 | 19971028 | 0 | |
| 126065831 | 12606583 | 5 | 20000317 | 0 | ||
| 126065831 | 12606583 | 6 | 20020618 | 0 |