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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127666371 | 12766637 | 1 | I | 20160906 | 20160921 | 20160921 | EXP | AU-VALIDUS PHARMACEUTICALS LLC-AU-2016VAL002669 | VALIDUS | KENNARD A, ROBERTS DM.. TRIMETHOPRIM-INDUCED CRITICAL HYPERKALAEMIA.. AUST PRESCR.. 2016;39 (4):136-7 | 88.00 | YR | F | Y | 0.00000 | 20160921 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127666371 | 12766637 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | UNK | Y | 16273 | |||||||||
| 127666371 | 12766637 | 2 | SS | QUINAPRIL HYDROCHLORIDE. | QUINAPRIL HYDROCHLORIDE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127666371 | 12766637 | 3 | SS | NEBIVOLOL HYDROCHLORIDE | NEBIVOLOL HYDROCHLORIDE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127666371 | 12766637 | 4 | SS | PREGABALIN. | PREGABALIN | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127666371 | 12766637 | 5 | SS | DOXEPIN | DOXEPIN | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127666371 | 12766637 | 6 | SS | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | Unknown | UNK | Y | Y | 0 | ||||||||
| 127666371 | 12766637 | 7 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127666371 | 12766637 | 8 | C | WARFARIN | WARFARIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127666371 | 12766637 | 9 | C | HEXAMINE HIPPURATE | 2 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127666371 | 12766637 | 1 | Product used for unknown indication |
| 127666371 | 12766637 | 2 | Product used for unknown indication |
| 127666371 | 12766637 | 3 | Product used for unknown indication |
| 127666371 | 12766637 | 4 | Product used for unknown indication |
| 127666371 | 12766637 | 5 | Product used for unknown indication |
| 127666371 | 12766637 | 6 | Urinary tract infection |
| 127666371 | 12766637 | 7 | Product used for unknown indication |
| 127666371 | 12766637 | 8 | Product used for unknown indication |
| 127666371 | 12766637 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127666371 | 12766637 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127666371 | 12766637 | Asthenia | |
| 127666371 | 12766637 | Bradycardia | |
| 127666371 | 12766637 | Delirium | |
| 127666371 | 12766637 | Hyperkalaemia | |
| 127666371 | 12766637 | Syncope |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |