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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126343081 | 12634308 | 1 | I | 200003 | 20160728 | 20160808 | 20160808 | EXP | GB-TEVA-681688ACC | TEVA | 47.00 | YR | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126343081 | 12634308 | 1 | PS | PAROXETINE. | PAROXETINE | 1 | 20 MILLIGRAM DAILY; 20 MG, QD | U | U | 76618 | 20 | MG | QD | ||||||
| 126343081 | 12634308 | 2 | SS | PAROXETINE. | PAROXETINE | 1 | 50 MILLIGRAM DAILY; 50 MG, QD | U | U | 76618 | 50 | MG | QD | ||||||
| 126343081 | 12634308 | 3 | SS | SEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Unknown | U | U | 0 | QD | ||||||||
| 126343081 | 12634308 | 4 | SS | CO-DYDRAMOL | ACETAMINOPHENDIHYDROCODEINE | 1 | Unknown | U | U | 0 | TABLET | ||||||||
| 126343081 | 12634308 | 5 | SS | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | U | U | 0 | TABLET | ||||||||
| 126343081 | 12634308 | 6 | C | FLUOXETINE HYDROCHLORIDE. | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 0 | 20 | MG | |||||||||
| 126343081 | 12634308 | 7 | C | PAROXETINE. | PAROXETINE | 1 | 0 | 30 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126343081 | 12634308 | 1 | Product used for unknown indication |
| 126343081 | 12634308 | 2 | Product used for unknown indication |
| 126343081 | 12634308 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126343081 | 12634308 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126343081 | 12634308 | Agitation | |
| 126343081 | 12634308 | Apathy | |
| 126343081 | 12634308 | Asthenia | |
| 126343081 | 12634308 | Decreased appetite | |
| 126343081 | 12634308 | Depressed mood | |
| 126343081 | 12634308 | Disturbance in attention | |
| 126343081 | 12634308 | Dizziness | |
| 126343081 | 12634308 | Headache | |
| 126343081 | 12634308 | Insomnia | |
| 126343081 | 12634308 | Nausea | |
| 126343081 | 12634308 | Overdose | |
| 126343081 | 12634308 | Paraesthesia | |
| 126343081 | 12634308 | Suicidal ideation | |
| 126343081 | 12634308 | Tearfulness | |
| 126343081 | 12634308 | Tension | |
| 126343081 | 12634308 | Vomiting | |
| 126343081 | 12634308 | 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 |
|---|---|---|---|---|---|---|
| 126343081 | 12634308 | 1 | 19991125 | 0 | ||
| 126343081 | 12634308 | 3 | 19991121 | 200306 | 0 | |
| 126343081 | 12634308 | 6 | 2003 | 0 |