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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378881 | 12537888 | 1 | I | 20160622 | 20160707 | 20160707 | EXP | LT-VALIDUS PHARMACEUTICALS LLC-LT-2016VAL002234 | VALIDUS | BILIUKAS M, KARPAVICIENE V. CARDIAC AMYLOIDOSIS. MEDICINOS. 2015;21(4.3):873-80 | 57.00 | YR | M | Y | 0.00000 | 20160707 | OT | LT | LT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378881 | 12537888 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | UNK | 17963 | |||||||||||
| 125378881 | 12537888 | 2 | SS | TORASEMIDE | TORSEMIDE | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 4 | SS | AMIODARONE | AMIODARONE | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 5 | SS | PERINDOPRIL | PERINDOPRIL | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 6 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 7 | SS | MILDRONATE | MELDONIUM | 1 | UNK | 0 | |||||||||||
| 125378881 | 12537888 | 8 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | UNK | U | 0 | ||||||||||
| 125378881 | 12537888 | 9 | C | WARFARIN | WARFARIN | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125378881 | 12537888 | 1 | Product used for unknown indication |
| 125378881 | 12537888 | 2 | Product used for unknown indication |
| 125378881 | 12537888 | 3 | Product used for unknown indication |
| 125378881 | 12537888 | 4 | Product used for unknown indication |
| 125378881 | 12537888 | 5 | Product used for unknown indication |
| 125378881 | 12537888 | 6 | Product used for unknown indication |
| 125378881 | 12537888 | 7 | Product used for unknown indication |
| 125378881 | 12537888 | 8 | Product used for unknown indication |
| 125378881 | 12537888 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125378881 | 12537888 | DE |
| 125378881 | 12537888 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125378881 | 12537888 | Cardiac failure acute | |
| 125378881 | 12537888 | Condition aggravated | |
| 125378881 | 12537888 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |