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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125369981 | 12536998 | 1 | I | 19951116 | 20160628 | 20160707 | 20160707 | EXP | PHHY2016GB089341 | SANDOZ | 39.00 | YR | F | Y | 0.00000 | 20160707 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125369981 | 12536998 | 1 | PS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | U | 75566 | ||||||||||
125369981 | 12536998 | 2 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 20 MG, QD | U | 75566 | 20 | MG | QD | ||||||
125369981 | 12536998 | 3 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 30 MG, QD | U | 75566 | 30 | MG | QD | ||||||
125369981 | 12536998 | 4 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | 20 MG, U | U | 0 | 20 | MG | |||||||
125369981 | 12536998 | 5 | C | PROTHIADEN | DOTHIEPIN HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
125369981 | 12536998 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
125369981 | 12536998 | 7 | C | ZIMOVANE | ZOPICLONE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125369981 | 12536998 | 1 | Product used for unknown indication |
125369981 | 12536998 | 4 | Product used for unknown indication |
125369981 | 12536998 | 5 | Muscle relaxant therapy |
125369981 | 12536998 | 6 | Product used for unknown indication |
125369981 | 12536998 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125369981 | 12536998 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125369981 | 12536998 | Agitation | |
125369981 | 12536998 | Asthenia | |
125369981 | 12536998 | Bedridden | |
125369981 | 12536998 | Depressed mood | |
125369981 | 12536998 | Disorientation | |
125369981 | 12536998 | Dizziness | |
125369981 | 12536998 | Headache | |
125369981 | 12536998 | Incontinence | |
125369981 | 12536998 | Increased tendency to bruise | |
125369981 | 12536998 | Insomnia | |
125369981 | 12536998 | Malaise | |
125369981 | 12536998 | Mood swings | |
125369981 | 12536998 | Nausea | |
125369981 | 12536998 | Nightmare | |
125369981 | 12536998 | Panic attack | |
125369981 | 12536998 | Suicidal ideation | |
125369981 | 12536998 | Tearfulness | |
125369981 | 12536998 | Tremor | |
125369981 | 12536998 | Vomiting | |
125369981 | 12536998 | 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 |
---|---|---|---|---|---|---|
125369981 | 12536998 | 1 | 19950810 | 0 | ||
125369981 | 12536998 | 2 | 19980305 | 19981223 | 0 | |
125369981 | 12536998 | 3 | 19980615 | 20011216 | 0 | |
125369981 | 12536998 | 4 | 19960328 | 19971028 | 0 | |
125369981 | 12536998 | 5 | 20000317 | 0 | ||
125369981 | 12536998 | 6 | 20020618 | 0 |