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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125629981 | 12562998 | 1 | I | 201606 | 20160704 | 20160715 | 20160715 | EXP | IT-TAKEDA-2016TUS012217 | TAKEDA | 62.00 | YR | F | Y | 0.00000 | 20160715 | CN | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125629981 | 12562998 | 1 | PS | BRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Oral | 10 GTT, QD | 204447 | 10 | GTT | TABLET | QD | ||||||
| 125629981 | 12562998 | 2 | SS | Elopram | CITALOPRAM HYDROBROMIDE | 1 | Oral | 40 MG, QD | 0 | 40 | MG | FILM-COATED TABLET | QD | ||||||
| 125629981 | 12562998 | 3 | SS | Elopram | CITALOPRAM HYDROBROMIDE | 1 | Oral | 80 MG, QD | 0 | 80 | MG | FILM-COATED TABLET | QD | ||||||
| 125629981 | 12562998 | 4 | SS | Elopram | CITALOPRAM HYDROBROMIDE | 1 | Oral | UNK | 0 | FILM-COATED TABLET | |||||||||
| 125629981 | 12562998 | 5 | SS | Elopram | CITALOPRAM HYDROBROMIDE | 1 | Oral | UNK | 0 | FILM-COATED TABLET | |||||||||
| 125629981 | 12562998 | 6 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | 120 MG, QD | 0 | 120 | MG | QD | |||||||
| 125629981 | 12562998 | 7 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | UNK UNK, QD | 0 | QD | |||||||||
| 125629981 | 12562998 | 8 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | UNK UNK, QD | 0 | QD | |||||||||
| 125629981 | 12562998 | 9 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | |||||||||
| 125629981 | 12562998 | 10 | C | EUTIROX/ LEVOTIROXINE | LEVOTHYROXINE SODIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 125629981 | 12562998 | 11 | C | Lorans/ lorazepam | 2 | Unknown | 1 MG, QD | U | 0 | 1 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125629981 | 12562998 | 1 | Depression |
| 125629981 | 12562998 | 2 | Depression |
| 125629981 | 12562998 | 6 | Depression |
| 125629981 | 12562998 | 9 | Diabetes mellitus |
| 125629981 | 12562998 | 10 | Autoimmune thyroiditis |
| 125629981 | 12562998 | 11 | Anxiety |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125629981 | 12562998 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125629981 | 12562998 | Drug ineffective | |
| 125629981 | 12562998 | Prescribed overdose | |
| 125629981 | 12562998 | Pruritus generalised | |
| 125629981 | 12562998 | Suicidal ideation |
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 |
|---|---|---|---|---|---|---|
| 125629981 | 12562998 | 1 | 20160616 | 0 | ||
| 125629981 | 12562998 | 2 | 201606 | 0 | ||
| 125629981 | 12562998 | 4 | 20160615 | 0 | ||
| 125629981 | 12562998 | 6 | 201606 | 0 | ||
| 125629981 | 12562998 | 7 | 20160615 | 0 |