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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126002661 | 12600266 | 1 | I | 20160119 | 20160713 | 20160727 | 20160727 | EXP | RE20160672 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002320 | VALIDUS | 75.00 | YR | M | Y | 0.00000 | 20160727 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126002661 | 12600266 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 0.25 DF, DAILY | Y | 16273 | .25 | DF | TABLET | ||||||
| 126002661 | 12600266 | 2 | SS | COUMADINE | WARFARIN SODIUM | 1 | Oral | 1 DF, AT BEDTIME | Y | UNKNOWN | 0 | 1 | DF | TABLET | |||||
| 126002661 | 12600266 | 3 | SS | COVERSYL /00790702/ | PERINDOPRIL | 1 | Oral | 5 MG, DAILY | U | UNKNOWN | 0 | 5 | MG | TABLET | |||||
| 126002661 | 12600266 | 4 | SS | GENTAMICIN /00047102/ | GENTAMICIN | 1 | Unknown | UNK | Y | UNKNOWN | 0 | ||||||||
| 126002661 | 12600266 | 5 | SS | CLOXACILLIN | CLOXACILLIN | 1 | Unknown | UNK | UNKNOWN | 0 | |||||||||
| 126002661 | 12600266 | 6 | C | SPECIAFOLDINE | FOLIC ACID | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 7 | C | TARDYFERON | FERROUS SULFATE | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 8 | C | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 9 | C | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 10 | C | LEVOTHYROX | LEVOTHYROXINE | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 11 | C | BISOPROLOL HEMIFUMARATE | BISOPROLOL FUMARATE | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 12 | C | DIFFU K | POTASSIUM CHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 126002661 | 12600266 | 13 | C | NOVONORM | REPAGLINIDE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126002661 | 12600266 | 1 | Product used for unknown indication |
| 126002661 | 12600266 | 2 | Atrial fibrillation |
| 126002661 | 12600266 | 3 | Hypertension |
| 126002661 | 12600266 | 4 | Product used for unknown indication |
| 126002661 | 12600266 | 5 | Product used for unknown indication |
| 126002661 | 12600266 | 6 | Product used for unknown indication |
| 126002661 | 12600266 | 7 | Product used for unknown indication |
| 126002661 | 12600266 | 8 | Product used for unknown indication |
| 126002661 | 12600266 | 9 | Product used for unknown indication |
| 126002661 | 12600266 | 10 | Product used for unknown indication |
| 126002661 | 12600266 | 11 | Product used for unknown indication |
| 126002661 | 12600266 | 12 | Product used for unknown indication |
| 126002661 | 12600266 | 13 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126002661 | 12600266 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126002661 | 12600266 | Acute kidney injury | |
| 126002661 | 12600266 | International normalised ratio increased | |
| 126002661 | 12600266 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 126002661 | 12600266 | 4 | 20160119 | 20160123 | 0 | |
| 126002661 | 12600266 | 5 | 20160119 | 0 |