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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125016562 | 12501656 | 2 | F | 20160530 | 20160627 | 20160728 | EXP | CH-009507513-1606CHE012509 | MERCK | PIETSCH U. MYOGLOBIN-INDUCED RENAL FAILURE AFTER CONCOMITANT ADMINISTRATION OF SIMVASTATIN AND AMIODARONE. ANAESTHESIST. 2016;1-3 | 74.00 | YR | M | Y | 0.00000 | 20160728 | MD | CH | CH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125016562 | 12501656 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | 40 MG, QD | Y | 19766 | 40 | MG | TABLET | QD | ||||||
| 125016562 | 12501656 | 2 | I | AMIODARONE | AMIODARONE | 1 | Oral | 200 MG PER DAY, MAINTENANCE THERAPY | Y | 0 | 200 | MG | QD | ||||||
| 125016562 | 12501656 | 3 | I | AMIODARONE | AMIODARONE | 1 | 10 G CUMULATIVE UNTIL THE NINTH DAY | Y | 0 | ||||||||||
| 125016562 | 12501656 | 4 | I | AMIODARONE | AMIODARONE | 1 | 10 G CUMULATIVE UNTIL THE NINTH DAY | Y | 0 | ||||||||||
| 125016562 | 12501656 | 5 | I | AMIODARONE | AMIODARONE | 1 | Oral | 200 MG PER DAY, MAINTENANCE THERAPY | Y | 0 | 200 | MG | QD | ||||||
| 125016562 | 12501656 | 6 | C | HEPARIN | HEPARIN SODIUM | 1 | U | 0 | |||||||||||
| 125016562 | 12501656 | 7 | C | FLOXACILLIN | FLUCLOXACILLIN | 1 | Intravenous (not otherwise specified) | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125016562 | 12501656 | 2 | Atrial fibrillation |
| 125016562 | 12501656 | 3 | Tachycardia |
| 125016562 | 12501656 | 7 | Antibiotic therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125016562 | 12501656 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125016562 | 12501656 | Drug interaction | |
| 125016562 | 12501656 | Renal failure | |
| 125016562 | 12501656 | Rhabdomyolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |