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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125739332 | 12573933 | 2 | F | 20160718 | 20160720 | 20160728 | EXP | GB-MHRA-MIDB-2F135602-2CEF-4B8E-9B56-A24B4036D804 | GB-TEVA-676640ACC | TEVA | 53.00 | YR | M | Y | 0.00000 | 20160728 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125739332 | 12573933 | 1 | PS | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | Oral | 20 MILLIGRAM DAILY; | Y | U | 78003 | 20 | MG | CAPSULE | QD | ||||
125739332 | 12573933 | 2 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 75 MILLIGRAM DAILY; | 0 | 75 | MG | TABLET | QD | ||||||
125739332 | 12573933 | 3 | C | BECLOMETHASONE | BECLOMETHASONE | 1 | Respiratory (inhalation) | 1000 MICROGRAM DAILY; INHALER | 0 | 500 | UG | BID | |||||||
125739332 | 12573933 | 4 | C | CARBAMAZEPINE. | CARBAMAZEPINE | 1 | Oral | 400 MILLIGRAM DAILY; | 0 | 200 | MG | TABLET | BID | ||||||
125739332 | 12573933 | 5 | C | PREGABALIN. | PREGABALIN | 1 | Oral | 200 MILLIGRAM DAILY; | 0 | 100 | MG | CAPSULE | BID | ||||||
125739332 | 12573933 | 6 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | 800 MICROGRAM DAILY; INHALER | 0 | 200 | UG | QID | |||||||
125739332 | 12573933 | 7 | C | THIAMINE. | THIAMINE | 1 | Oral | 200 MILLIGRAM DAILY; | 0 | 100 | MG | TABLET | BID | ||||||
125739332 | 12573933 | 8 | C | VITAMIN B COMPOUND STRONG | 2 | Oral | 2 DOSAGE FORMS DAILY; | 0 | 1 | DF | TABLET | BID |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125739332 | 12573933 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125739332 | 12573933 | Fall | |
125739332 | 12573933 | 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 |
---|---|---|---|---|---|---|
125739332 | 12573933 | 1 | 20160519 | 0 |