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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126948921 | 12694892 | 1 | I | 20140607 | 20160817 | 20160829 | 20160829 | EXP | US-MYLANLABS-2016M1034694 | MYLAN | 0.00 | Y | 0.00000 | 20160829 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126948921 | 12694892 | 1 | PS | DIGOXIN. | DIGOXIN | 1 | Oral | 0.125 MG, BID | 40282 | .125 | MG | TABLET | BID | ||||||
| 126948921 | 12694892 | 2 | SS | DIGOXIN. | DIGOXIN | 1 | UNK | 0 | TABLET | ||||||||||
| 126948921 | 12694892 | 3 | SS | DIGOXIN. | DIGOXIN | 1 | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126948921 | 12694892 | 1 | Cardiac failure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126948921 | 12694892 | DE |
| 126948921 | 12694892 | OT |
| 126948921 | 12694892 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126948921 | 12694892 | Blood pressure decreased | |
| 126948921 | 12694892 | Bradycardia | |
| 126948921 | 12694892 | Cardiac arrest | |
| 126948921 | 12694892 | Dizziness | |
| 126948921 | 12694892 | Hypotension | |
| 126948921 | 12694892 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |