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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125740332 | 12574033 | 2 | F | 19950523 | 20160727 | 20160720 | 20160808 | EXP | GB-TEVA-676623ACC | TEVA | 17.00 | YR | F | Y | 0.00000 | 20160808 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125740332 | 12574033 | 1 | SS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | UNK | U | U | 0 | ||||||||
125740332 | 12574033 | 2 | PS | PAROXETINE. | PAROXETINE | 1 | Unknown | UNK | U | U | 76618 | TABLET | |||||||
125740332 | 12574033 | 3 | SS | ETHANOL | ALCOHOL | 1 | Unknown | UNK | U | U | 0 | ||||||||
125740332 | 12574033 | 4 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK | Y | U | 0 | TABLET | |||||||
125740332 | 12574033 | 5 | C | IMIPRAMINE | IMIPRAMINE | 1 | UNK | 0 | |||||||||||
125740332 | 12574033 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
125740332 | 12574033 | 7 | C | ST JOHNS WORT | ST. JOHN'S WORT | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125740332 | 12574033 | 1 | Product used for unknown indication |
125740332 | 12574033 | 2 | Product used for unknown indication |
125740332 | 12574033 | 3 | Product used for unknown indication |
125740332 | 12574033 | 4 | Depression |
125740332 | 12574033 | 5 | Product used for unknown indication |
125740332 | 12574033 | 6 | Product used for unknown indication |
125740332 | 12574033 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125740332 | 12574033 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125740332 | 12574033 | Aggression | |
125740332 | 12574033 | Anxiety | |
125740332 | 12574033 | Binge eating | |
125740332 | 12574033 | Crying | |
125740332 | 12574033 | Depression | |
125740332 | 12574033 | Derealisation | |
125740332 | 12574033 | Drug withdrawal syndrome | |
125740332 | 12574033 | Fatigue | |
125740332 | 12574033 | Hunger | |
125740332 | 12574033 | Mood swings | |
125740332 | 12574033 | Nightmare | |
125740332 | 12574033 | Overdose | |
125740332 | 12574033 | Social avoidant behaviour | |
125740332 | 12574033 | Suicide attempt | |
125740332 | 12574033 | Tearfulness |
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 |
---|---|---|---|---|---|---|
125740332 | 12574033 | 4 | 19950512 | 0 | ||
125740332 | 12574033 | 5 | 19950922 | 0 | ||
125740332 | 12574033 | 6 | 19960131 | 1999 | 0 | |
125740332 | 12574033 | 7 | 1999 | 2005 | 0 |