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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125699191 | 12569919 | 1 | I | 200003 | 20041203 | 20160719 | 20160719 | EXP | GB-GLAXOSMITHKLINE-B0359599A | GLAXOSMITHKLINE | 31.36 | YR | M | Y | 0.00000 | 20160719 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125699191 | 12569919 | 1 | PS | Seroxat | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK, 1D | U | 20031 | QD | ||||||||
125699191 | 12569919 | 2 | SS | PAROXETINE. | PAROXETINE | 1 | 20 MG, QD | U | 20031 | 20 | MG | QD | |||||||
125699191 | 12569919 | 3 | SS | PAROXETINE. | PAROXETINE | 1 | 50 MG, QD | U | 20031 | 50 | MG | QD | |||||||
125699191 | 12569919 | 4 | SS | Paracetamol | ACETAMINOPHEN | 1 | Unknown | UNK | U | 0 | |||||||||
125699191 | 12569919 | 5 | SS | CO-DYDRAMOL | ACETAMINOPHENDIHYDROCODEINE | 1 | Unknown | UNK | U | 0 | |||||||||
125699191 | 12569919 | 6 | C | FLUOXETINE HYDROCHLORIDE. | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125699191 | 12569919 | 1 | Product used for unknown indication |
125699191 | 12569919 | 2 | Product used for unknown indication |
125699191 | 12569919 | 4 | Product used for unknown indication |
125699191 | 12569919 | 5 | Product used for unknown indication |
125699191 | 12569919 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125699191 | 12569919 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125699191 | 12569919 | Agitation | |
125699191 | 12569919 | Apathy | |
125699191 | 12569919 | Asthenia | |
125699191 | 12569919 | Decreased appetite | |
125699191 | 12569919 | Depressed mood | |
125699191 | 12569919 | Depression | |
125699191 | 12569919 | Disturbance in attention | |
125699191 | 12569919 | Dizziness | |
125699191 | 12569919 | Headache | |
125699191 | 12569919 | Insomnia | |
125699191 | 12569919 | Nausea | |
125699191 | 12569919 | Overdose | |
125699191 | 12569919 | Paraesthesia | |
125699191 | 12569919 | Suicidal ideation | |
125699191 | 12569919 | Tearfulness | |
125699191 | 12569919 | Tension | |
125699191 | 12569919 | Vomiting | |
125699191 | 12569919 | 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 |
---|---|---|---|---|---|---|
125699191 | 12569919 | 1 | 19991121 | 200306 | 0 |