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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126389871 | 12638987 | 1 | I | 20160725 | 20160809 | 20160809 | EXP | AU-TAKEDA-2016TEU004280 | TAKEDA | BARTON J, WONG A, GRAUDINS A.. ANTI-XA ACTIVITY IN APIXABAN OVERDOSE: A CASE REPORT. CLIN-TOXICOL-(PHILA). 2016;1-6 | 53.00 | YR | M | Y | 0.00000 | 20160809 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126389871 | 12638987 | 1 | PS | COLCHICINE. | COLCHICINE | 1 | Unknown | 6 MG, UNK | 22352 | 6 | MG | ||||||||
| 126389871 | 12638987 | 2 | SS | Bisoprolol | BISOPROLOL | 1 | Unknown | 105 MG, UNK | 0 | 105 | MG | ||||||||
| 126389871 | 12638987 | 3 | SS | Atorvastatin | ATORVASTATIN | 1 | Unknown | 280 MG, UNK | 0 | 280 | MG | ||||||||
| 126389871 | 12638987 | 4 | SS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 35 MG, UNK | 0 | 35 | MG | ||||||||
| 126389871 | 12638987 | 5 | SS | Magnesium | MAGNESIUM | 1 | Unknown | 37.4 MG, UNK | 0 | 37.4 | MG | ||||||||
| 126389871 | 12638987 | 6 | SS | APIXABAN | APIXABAN | 1 | Unknown | 200 MG, UNK | 0 | 200 | MG | ||||||||
| 126389871 | 12638987 | 7 | SS | CODEINE PHOSPHATE W/PARACETAMOL/PHENYLEPHRINE | ACETAMINOPHENCODEINEPHENYLEPHRINE | 1 | Unknown | FOUR UNITS OF 500 MG PARACETAMOL/9.5 MG CODEINE/5 MG PHENYLEPHRINE,UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126389871 | 12638987 | 1 | Product used for unknown indication |
| 126389871 | 12638987 | 2 | Product used for unknown indication |
| 126389871 | 12638987 | 3 | Product used for unknown indication |
| 126389871 | 12638987 | 4 | Product used for unknown indication |
| 126389871 | 12638987 | 5 | Product used for unknown indication |
| 126389871 | 12638987 | 6 | Atrial fibrillation |
| 126389871 | 12638987 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126389871 | 12638987 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126389871 | 12638987 | Haemorrhage | |
| 126389871 | 12638987 | Hypotension | |
| 126389871 | 12638987 | Intentional overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |