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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125418381 | 12541838 | 1 | I | 20031023 | 20160627 | 20160708 | 20160708 | EXP | GB-TEVA-673555ACC | TEVA | 0.00 | M | Y | 0.00000 | 20160708 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125418381 | 12541838 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | UNK | 10360 | MG | U | U | 76618 | TABLET | ||||||
125418381 | 12541838 | 2 | SS | PAROXETINE. | PAROXETINE | 1 | Unknown | UNK UNK, U | 10360 | MG | U | U | 76618 | TABLET | |||||
125418381 | 12541838 | 3 | SS | PAROXETINE. | PAROXETINE | 1 | Oral | 40 MILLIGRAM DAILY; 20 MG, BID | 10360 | MG | U | U | 76618 | 20 | MG | TABLET | BID | ||
125418381 | 12541838 | 4 | SS | CO-DYDRAMOL | ACETAMINOPHENDIHYDROCODEINE | 1 | Unknown | U | U | 0 | |||||||||
125418381 | 12541838 | 5 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | 5 ML DAILY; 5 ML, QD | 210.208333 | ML | U | U | 0 | 5 | ML | ORAL SOLUTION | QD | ||
125418381 | 12541838 | 6 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | 210.208333 | ML | U | U | 0 | |||||||
125418381 | 12541838 | 7 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Oral | 40 MILLIGRAM DAILY; 20 MG, BID | 40 | MG | U | U | 0 | 20 | MG | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125418381 | 12541838 | 1 | Depression |
125418381 | 12541838 | 4 | Product used for unknown indication |
125418381 | 12541838 | 5 | Depression |
125418381 | 12541838 | 6 | Depression |
125418381 | 12541838 | 7 | Depression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125418381 | 12541838 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125418381 | 12541838 | Abnormal behaviour | |
125418381 | 12541838 | Aggression | |
125418381 | 12541838 | Agitation | |
125418381 | 12541838 | Anxiety | |
125418381 | 12541838 | Chest pain | |
125418381 | 12541838 | Disorientation | |
125418381 | 12541838 | Disturbance in attention | |
125418381 | 12541838 | Dizziness | |
125418381 | 12541838 | Fatigue | |
125418381 | 12541838 | Flat affect | |
125418381 | 12541838 | Headache | |
125418381 | 12541838 | Hyperhidrosis | |
125418381 | 12541838 | Impulsive behaviour | |
125418381 | 12541838 | Insomnia | |
125418381 | 12541838 | Judgement impaired | |
125418381 | 12541838 | Legal problem | |
125418381 | 12541838 | Lethargy | |
125418381 | 12541838 | Memory impairment | |
125418381 | 12541838 | Mood swings | |
125418381 | 12541838 | Nausea | |
125418381 | 12541838 | Nightmare | |
125418381 | 12541838 | Panic attack | |
125418381 | 12541838 | Paraesthesia | |
125418381 | 12541838 | Personality change | |
125418381 | 12541838 | Sleep disorder | |
125418381 | 12541838 | Suicidal ideation | |
125418381 | 12541838 | Syncope | |
125418381 | 12541838 | Tremor | |
125418381 | 12541838 | Vertigo | |
125418381 | 12541838 | Vomiting | |
125418381 | 12541838 | 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 |
---|---|---|---|---|---|---|
125418381 | 12541838 | 2 | 200111 | 0 | ||
125418381 | 12541838 | 3 | 20030206 | 20031204 | 0 | |
125418381 | 12541838 | 4 | 200111 | 0 | ||
125418381 | 12541838 | 5 | 20031204 | 0 | ||
125418381 | 12541838 | 7 | 20031023 | 0 |