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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127363901 | 12736390 | 1 | I | 20160830 | 20160913 | 20160913 | EXP | AU-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123729 | RANBAXY | 88.00 | YR | F | Y | 0.00000 | 20160913 | OT | GB | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127363901 | 12736390 | 1 | SS | PREGABALIN. | PREGABALIN | 1 | Unknown | UNK | Y | U | 0 | ||||||||
127363901 | 12736390 | 2 | SS | NEBIVOLOL. | NEBIVOLOL | 1 | Unknown | UNK | Y | U | 0 | ||||||||
127363901 | 12736390 | 3 | PS | Doxepin | DOXEPIN | 1 | Unknown | UNK | Y | U | 71502 | ||||||||
127363901 | 12736390 | 4 | SS | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | Unknown | UNK | Y | Y | 0 | ||||||||
127363901 | 12736390 | 5 | C | WARFARIN | WARFARIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
127363901 | 12736390 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
127363901 | 12736390 | 7 | C | QUINAPRIL. | QUINAPRIL | 1 | Unknown | UNK | Y | U | 0 | ||||||||
127363901 | 12736390 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | UNK | Y | U | 0 | ||||||||
127363901 | 12736390 | 9 | C | HEXAMINE HIPPURATE | 2 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127363901 | 12736390 | 1 | Product used for unknown indication |
127363901 | 12736390 | 2 | Product used for unknown indication |
127363901 | 12736390 | 3 | Product used for unknown indication |
127363901 | 12736390 | 4 | Urinary tract infection |
127363901 | 12736390 | 5 | Product used for unknown indication |
127363901 | 12736390 | 6 | Product used for unknown indication |
127363901 | 12736390 | 7 | Product used for unknown indication |
127363901 | 12736390 | 8 | Product used for unknown indication |
127363901 | 12736390 | 9 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127363901 | 12736390 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127363901 | 12736390 | Hyperkalaemia | Hyperkalaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |