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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127835101 | 12783510 | 1 | I | 20160820 | 20160913 | 20160927 | 20160927 | EXP | AM20161087 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002673 | VALIDUS | 83.00 | YR | F | Y | 0.00000 | 20160927 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127835101 | 12783510 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 1 DOSAGE FORM;DAILY | Y | U | 16273 | 1 | DF | ||||||
| 127835101 | 12783510 | 2 | SS | CANDESARTAN CILEXETIL. | CANDESARTAN CILEXETIL | 1 | Oral | 32 MILLIGRAM(S); DAILY | Y | U | 0 | 32 | MG | ||||||
| 127835101 | 12783510 | 3 | SS | ALDACTAZINE | ALTHIAZIDESPIRONOLACTONE | 1 | Oral | 1 DOSAGE FORM;DAILY | Y | U | 0 | 1 | DF | ||||||
| 127835101 | 12783510 | 4 | C | UMULINE | INSULIN HUMAN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 5 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 6 | C | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 7 | C | ACEBUTOLOL | ACEBUTOLOL | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 8 | C | STAGID | METFORMIN PAMOATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 9 | C | DOLIPRANE | ACETAMINOPHEN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127835101 | 12783510 | 10 | C | FONX | 2 | Unknown | UNK | U | 0 | ||||||||||
| 127835101 | 12783510 | 11 | C | CYTEAL | CHLORHEXIDINE GLUCONATECHLOROCRESOLHEXAMIDINE DIISETHIONATE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127835101 | 12783510 | 1 | Product used for unknown indication |
| 127835101 | 12783510 | 2 | Product used for unknown indication |
| 127835101 | 12783510 | 3 | Product used for unknown indication |
| 127835101 | 12783510 | 4 | Product used for unknown indication |
| 127835101 | 12783510 | 5 | Product used for unknown indication |
| 127835101 | 12783510 | 6 | Product used for unknown indication |
| 127835101 | 12783510 | 7 | Product used for unknown indication |
| 127835101 | 12783510 | 8 | Product used for unknown indication |
| 127835101 | 12783510 | 9 | Product used for unknown indication |
| 127835101 | 12783510 | 10 | Product used for unknown indication |
| 127835101 | 12783510 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127835101 | 12783510 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127835101 | 12783510 | Acute kidney injury | |
| 127835101 | 12783510 | Hyperkalaemia |
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 |
|---|---|---|---|---|---|---|
| 127835101 | 12783510 | 1 | 20160820 | 0 | ||
| 127835101 | 12783510 | 2 | 20160820 | 0 | ||
| 127835101 | 12783510 | 3 | 20160820 | 0 |