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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125899691 | 12589969 | 1 | I | 20160714 | 20160725 | 20160725 | EXP | PHHY2016NO097385 | SANDOZ | 0.00 | A | M | Y | 0.00000 | 20160725 | OT | NO | NO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125899691 | 12589969 | 1 | PS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Unknown | 77040 | FILM-COATED TABLET | ||||||||||
| 125899691 | 12589969 | 2 | SS | LAMOTRIGINE. | LAMOTRIGINE | 1 | Unknown | 0 | |||||||||||
| 125899691 | 12589969 | 3 | SS | ZOPICLONE | ZOPICLONE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125899691 | 12589969 | 1 | Depressed level of consciousness |
| 125899691 | 12589969 | 2 | Depressed level of consciousness |
| 125899691 | 12589969 | 3 | Depressed level of consciousness |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125899691 | 12589969 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125899691 | 12589969 | Accidental poisoning | |
| 125899691 | 12589969 | Drug therapy enhancement |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |