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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126801041 | 12680104 | 1 | I | 20160311 | 20160316 | 20160824 | 20160824 | PER | US-FRI-1000083397 | FOREST | 42.68 | YR | M | Y | 86.18000 | KG | 20160824 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126801041 | 12680104 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | 20MG | Y | 21323 | 20 | MG | TABLET | QD | |||||
| 126801041 | 12680104 | 2 | SS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Y | 21323 | |||||||||||
| 126801041 | 12680104 | 3 | SS | BENAZEPRIL | BENAZEPRIL HYDROCHLORIDE | 1 | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126801041 | 12680104 | 1 | Anxiety |
| 126801041 | 12680104 | 2 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126801041 | 12680104 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126801041 | 12680104 | Paraesthesia | |
| 126801041 | 12680104 | Serotonin syndrome | |
| 126801041 | 12680104 | Wrong patient received medication |
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 |
|---|---|---|---|---|---|---|
| 126801041 | 12680104 | 1 | 2011 | 20160316 | 0 |