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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125825192 | 12582519 | 2 | F | 20160718 | 20160722 | 20160801 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120688 | RANBAXY | 53.00 | YR | M | Y | 0.00000 | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125825192 | 12582519 | 1 | PS | Esomeprazole | ESOMEPRAZOLE | 1 | Oral | 20 MG, DAILY | Y | U | 200882 | 20 | MG | ||||||
| 125825192 | 12582519 | 2 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 75 MG, DAILY | U | U | 0 | 75 | MG | ||||||
| 125825192 | 12582519 | 3 | C | BECLOMETHASONE | BECLOMETHASONE | 1 | Respiratory (inhalation) | 500 ?G, BID | U | U | 0 | 500 | UG | Q12H | |||||
| 125825192 | 12582519 | 4 | C | CARBAMAZEPINE. | CARBAMAZEPINE | 1 | Oral | 200 MG, BID | U | U | 0 | 200 | MG | Q12H | |||||
| 125825192 | 12582519 | 5 | C | PREGABALIN. | PREGABALIN | 1 | Oral | 100 MG, BID | U | U | 0 | 100 | MG | Q12H | |||||
| 125825192 | 12582519 | 6 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | 200 ?G, QID | U | U | 0 | 200 | UG | Q6H | |||||
| 125825192 | 12582519 | 7 | C | THIAMINE. | THIAMINE | 1 | Oral | 100 MG, BID | U | U | 0 | 100 | MG | Q12H | |||||
| 125825192 | 12582519 | 8 | C | VITAMIN B COMPOUND STRONG | 2 | Oral | 1 DF, BID | U | U | 0 | 1 | DF | Q12H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125825192 | 12582519 | 1 | Product used for unknown indication |
| 125825192 | 12582519 | 2 | Product used for unknown indication |
| 125825192 | 12582519 | 3 | Product used for unknown indication |
| 125825192 | 12582519 | 4 | Product used for unknown indication |
| 125825192 | 12582519 | 5 | Product used for unknown indication |
| 125825192 | 12582519 | 6 | Product used for unknown indication |
| 125825192 | 12582519 | 7 | Product used for unknown indication |
| 125825192 | 12582519 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125825192 | 12582519 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125825192 | 12582519 | Fall | |
| 125825192 | 12582519 | Hyponatraemia |
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 |
|---|---|---|---|---|---|---|
| 125825192 | 12582519 | 1 | 20160519 | 0 |