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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124979073 | 12497907 | 3 | F | 199712 | 20160712 | 20160625 | 20160726 | EXP | GB-APOTEX-2016AP009466 | APOTEX | 36.00 | YR | M | Y | 0.00000 | 20160726 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124979073 | 12497907 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | Unknown | 20 MG, QD | U | U | 20031 | 20 | MG | TABLET | |||||
124979073 | 12497907 | 2 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | TABLET | |||||||
124979073 | 12497907 | 3 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | TABLET | |||||||
124979073 | 12497907 | 4 | C | LITHIUM CARBONATE. | LITHIUM CARBONATE | 1 | Unknown | 40 MG, NOCTE | U | U | 0 | 40 | MG | QD | |||||
124979073 | 12497907 | 5 | C | ZOPICLONE | ZOPICLONE | 1 | Unknown | 7.5 MG, UNKNOWN | U | U | 0 | 7.5 | MG | ||||||
124979073 | 12497907 | 6 | C | PROCYCLIDINE | PROCYCLIDINE | 1 | Unknown | 5 MG, TID | U | U | 0 | 5 | MG | TID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124979073 | 12497907 | 1 | Bipolar disorder |
124979073 | 12497907 | 2 | Product used for unknown indication |
124979073 | 12497907 | 3 | Product used for unknown indication |
124979073 | 12497907 | 4 | Product used for unknown indication |
124979073 | 12497907 | 5 | Product used for unknown indication |
124979073 | 12497907 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124979073 | 12497907 | HO |
124979073 | 12497907 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124979073 | 12497907 | Aggression | |
124979073 | 12497907 | Agitation | |
124979073 | 12497907 | Anger | |
124979073 | 12497907 | Anxiety | |
124979073 | 12497907 | Asthenia | |
124979073 | 12497907 | Burning sensation | |
124979073 | 12497907 | Decreased appetite | |
124979073 | 12497907 | Depressed mood | |
124979073 | 12497907 | Disturbance in attention | |
124979073 | 12497907 | Dizziness | |
124979073 | 12497907 | Drug withdrawal syndrome | |
124979073 | 12497907 | Dyskinesia | |
124979073 | 12497907 | Energy increased | |
124979073 | 12497907 | Fatigue | |
124979073 | 12497907 | Flushing | |
124979073 | 12497907 | Head titubation | |
124979073 | 12497907 | Headache | |
124979073 | 12497907 | Hypoaesthesia | |
124979073 | 12497907 | Insomnia | |
124979073 | 12497907 | Irritability | |
124979073 | 12497907 | Malaise | |
124979073 | 12497907 | Mania | |
124979073 | 12497907 | Mood altered | |
124979073 | 12497907 | Pain | |
124979073 | 12497907 | Panic attack | |
124979073 | 12497907 | Paraesthesia | |
124979073 | 12497907 | Personality change | |
124979073 | 12497907 | Rash | |
124979073 | 12497907 | Restlessness | |
124979073 | 12497907 | Skin reaction | |
124979073 | 12497907 | Suicidal ideation | |
124979073 | 12497907 | Suicide attempt | |
124979073 | 12497907 | Tremor |
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 |
---|---|---|---|---|---|---|
124979073 | 12497907 | 1 | 19971113 | 0 | ||
124979073 | 12497907 | 2 | 19970916 | 0 | ||
124979073 | 12497907 | 3 | 19970916 | 0 |