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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127044523 | 12704452 | 3 | F | 20160909 | 20160831 | 20160921 | EXP | GB-MHRA-EYC 00143803 | GB-TEVA-687358ACC | TEVA | 99.00 | YR | F | Y | 70.00000 | KG | 20160921 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127044523 | 12704452 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 60 MILLIGRAM DAILY; 20MG DAILY BUT INCREASED IN DAYS PRIOR TO HOSPITAL ADMISSION TO 60MG DAILY | Y | U | 18413 | 60 | MG | QD | |||||
127044523 | 12704452 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 20 MILLIGRAM DAILY; 20MG DAILY BUT INCREASED IN DAYS PRIOR TO HOSPITAL ADMISSION TO 60MG DAILY | Y | U | 18413 | 20 | MG | QD | |||||
127044523 | 12704452 | 3 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MILLIGRAM DAILY; | U | U | 75347 | 20 | MG | QD | |||||
127044523 | 12704452 | 4 | SS | MIRTAZAPINE. | MIRTAZAPINE | 1 | Oral | 15 MILLIGRAM DAILY; | U | U | 76119 | 15 | MG | QD | |||||
127044523 | 12704452 | 5 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 12.5 MILLIGRAM DAILY; | U | U | 0 | 12.5 | MG | QD | |||||
127044523 | 12704452 | 6 | C | CALCICHEW D3 | CALCIUMCHOLECALCIFEROL | 1 | 0 | ||||||||||||
127044523 | 12704452 | 7 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | 0 | |||||||||||
127044523 | 12704452 | 8 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
127044523 | 12704452 | 9 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | PRESSURISED INHALATION, SUSPENSION | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127044523 | 12704452 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127044523 | 12704452 | Acute kidney injury | |
127044523 | 12704452 | Confusional state | |
127044523 | 12704452 | Hyponatraemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |