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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126714051 | 12671405 | 1 | I | 20160809 | 20160822 | 20160822 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122165 | RANBAXY | 41.00 | YR | F | Y | 58.96000 | KG | 20160822 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126714051 | 12671405 | 1 | PS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | ALTERNATING WITH 7.5MG | U | U | 77032 | 5 | MG | ||||||
| 126714051 | 12671405 | 2 | SS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | ALTERNATING WITH 5MG | U | U | 77032 | 7.5 | MG | ||||||
| 126714051 | 12671405 | 3 | SS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | 10 MG, UNK | U | U | 77032 | 10 | MG | ||||||
| 126714051 | 12671405 | 4 | SS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | 20 MG, UNK | U | U | 77032 | 20 | MG | ||||||
| 126714051 | 12671405 | 5 | C | ACTAVIS UK PREDNISOLONE | 2 | Unknown | U | U | 0 | ||||||||||
| 126714051 | 12671405 | 6 | C | GENERICS UK SULPHASALAZINE | 2 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126714051 | 12671405 | 1 | Anxiety |
| 126714051 | 12671405 | 2 | Anxiety |
| 126714051 | 12671405 | 5 | Product used for unknown indication |
| 126714051 | 12671405 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126714051 | 12671405 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126714051 | 12671405 | Blood pressure decreased | |
| 126714051 | 12671405 | Heart rate abnormal | |
| 126714051 | 12671405 | Palpitations | |
| 126714051 | 12671405 | Syncope | |
| 126714051 | 12671405 | Ventricular tachycardia |
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 |
|---|---|---|---|---|---|---|
| 126714051 | 12671405 | 5 | 1997 | 0 |