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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127063311 | 12706331 | 1 | I | 20160818 | 20160901 | 20160901 | EXP | GB-AUROBINDO-AUR-APL-2016-10778 | AUROBINDO | 99.00 | YR | F | Y | 70.00000 | KG | 20160901 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127063311 | 12706331 | 1 | SS | Furosemide 20 mg | FUROSEMIDE | 1 | Oral | 20 MG, ONCE A DAY | Y | U | 0 | 20 | MG | QD | |||||
127063311 | 12706331 | 2 | SS | Furosemide 20 mg | FUROSEMIDE | 1 | Oral | 60 MG, DAILY | Y | U | 0 | 60 | MG | ||||||
127063311 | 12706331 | 3 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MG, ONCE A DAY | U | U | 203270 | 20 | MG | QD | |||||
127063311 | 12706331 | 4 | SS | Mirtazapine 15mg | MIRTAZAPINE | 1 | Oral | 15 MG, ONCE A DAY | U | U | 0 | 15 | MG | QD | |||||
127063311 | 12706331 | 5 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 12.5 MG, ONCE A DAY | U | U | 0 | 12.5 | MG | QD | |||||
127063311 | 12706331 | 6 | C | CALCICHEW D3 | CALCIUMCHOLECALCIFEROL | 1 | Unknown | U | 0 | ||||||||||
127063311 | 12706331 | 7 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | U | 0 | ||||||||||
127063311 | 12706331 | 8 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | U | 0 | ||||||||||
127063311 | 12706331 | 9 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | U | 0 | PRESSURISED INHALATION, SUSPENSION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127063311 | 12706331 | 1 | Product used for unknown indication |
127063311 | 12706331 | 3 | Product used for unknown indication |
127063311 | 12706331 | 4 | Product used for unknown indication |
127063311 | 12706331 | 5 | Product used for unknown indication |
127063311 | 12706331 | 6 | Product used for unknown indication |
127063311 | 12706331 | 7 | Product used for unknown indication |
127063311 | 12706331 | 8 | Product used for unknown indication |
127063311 | 12706331 | 9 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127063311 | 12706331 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127063311 | 12706331 | Acute kidney injury | |
127063311 | 12706331 | Confusional state | |
127063311 | 12706331 | Fall | |
127063311 | 12706331 | Hyponatraemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |