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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127134441 | 12713444 | 1 | I | 20160822 | 20160903 | 20160903 | EXP | GB-AUROBINDO-AUR-APL-2016-10885 | AUROBINDO | 0.00 | A | F | Y | 0.00000 | 20160903 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127134441 | 12713444 | 1 | PS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Unknown | 30 MG, (PAST DRUG) | U | U | 77031 | 30 | MG | ||||||
| 127134441 | 12713444 | 2 | SS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Unknown | 12 MG, (CURRENT DRUG) | U | U | 77031 | 12 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127134441 | 12713444 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127134441 | 12713444 | OT |
| 127134441 | 12713444 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127134441 | 12713444 | Abdominal pain upper | |
| 127134441 | 12713444 | Chills | |
| 127134441 | 12713444 | Constipation | |
| 127134441 | 12713444 | Critical illness | |
| 127134441 | 12713444 | Diarrhoea | |
| 127134441 | 12713444 | Hyperhidrosis | |
| 127134441 | 12713444 | Nausea | |
| 127134441 | 12713444 | Vomiting | |
| 127134441 | 12713444 | Withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |