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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281931 | 12528193 | 1 | I | 20160624 | 20160705 | 20160705 | EXP | GB-SYMPLMED PHARMACEUTICALS-2016SYMPLMED000255 | SYMPLMED PHARMACEUTICALS | 0.00 | Y | 0.00000 | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281931 | 12528193 | 1 | PS | PERINDOPRIL ERBUMINE. | PERINDOPRIL ERBUMINE | 1 | Unknown | 4 MG, QD | Y | U | UNKNOWN | 20184 | 4 | MG | TABLET | ||||
| 125281931 | 12528193 | 2 | SS | BUMETANIDE. | BUMETANIDE | 1 | Unknown | 16 MG, QD | Y | U | UNKNOWN | 0 | 16 | MG | |||||
| 125281931 | 12528193 | 3 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | 25 MG, QD | Y | U | UNKNOWN | 0 | 25 | MG | |||||
| 125281931 | 12528193 | 4 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | 75 MG, QD | U | UNKNOWN | 0 | 75 | MG | |||||||
| 125281931 | 12528193 | 5 | C | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | 120 MG, QD | U | UNKNOWN | 0 | 120 | MG | |||||||
| 125281931 | 12528193 | 6 | C | FINASTERIDE. | FINASTERIDE | 1 | 5 MG, QD | U | UNKNOWN | 0 | 5 | MG | |||||||
| 125281931 | 12528193 | 7 | C | ISOSORBIDE MONONITRATE. | ISOSORBIDE MONONITRATE | 1 | 60 MG, QD | U | UNKNOWN | 0 | 60 | MG | |||||||
| 125281931 | 12528193 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 20 MG, QD | U | UNKNOWN | 0 | 20 | MG | |||||||
| 125281931 | 12528193 | 9 | C | PRAVASTATIN. | PRAVASTATIN | 1 | 40 MG, QD | U | UNKNOWN | 0 | 40 | MG | |||||||
| 125281931 | 12528193 | 10 | C | TAMSULOSIN | TAMSULOSIN | 1 | 400 ?G, QD | U | UNKNOWN | 0 | 400 | UG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125281931 | 12528193 | 1 | Product used for unknown indication |
| 125281931 | 12528193 | 2 | Product used for unknown indication |
| 125281931 | 12528193 | 3 | Product used for unknown indication |
| 125281931 | 12528193 | 4 | Product used for unknown indication |
| 125281931 | 12528193 | 5 | Product used for unknown indication |
| 125281931 | 12528193 | 6 | Product used for unknown indication |
| 125281931 | 12528193 | 7 | Product used for unknown indication |
| 125281931 | 12528193 | 8 | Product used for unknown indication |
| 125281931 | 12528193 | 9 | Product used for unknown indication |
| 125281931 | 12528193 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125281931 | 12528193 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125281931 | 12528193 | Acute kidney injury | |
| 125281931 | 12528193 | Anaemia | |
| 125281931 | 12528193 | Dehydration |
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 |
|---|---|---|---|---|---|---|
| 125281931 | 12528193 | 1 | 20160522 | 0 | ||
| 125281931 | 12528193 | 2 | 20160522 | 0 | ||
| 125281931 | 12528193 | 3 | 20160522 | 0 |