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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126470921 | 12647092 | 1 | I | 20160729 | 20160812 | 20160812 | EXP | AU-MLMSERVICE-20160801-0376507-1 | AU-LUPIN PHARMACEUTICALS INC.-2016-03507 | LUPIN | BARTON J, WONG A, GRAUDINS A. ANTI-XA ACTIVITY IN APIXABAN OVERDOSE: A CASE REPORT. CLINICAL TOXICOLOGY. 2016;1-3. | 53.00 | YR | M | Y | 0.00000 | 20160812 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126470921 | 12647092 | 1 | SS | Apixaban | APIXABAN | 1 | Unknown | 40 X 5MG | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 2 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 28 X 1.25MG | UNKNOWN | 77626 | |||||||||
| 126470921 | 12647092 | 3 | SS | Bisoprolol | BISOPROLOL | 1 | Unknown | 42 X 2.5MG | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 4 | SS | Atorvastatin | ATORVASTATIN | 1 | Unknown | 7 X 40 MG | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 5 | SS | COLCHICINE. | COLCHICINE | 1 | Unknown | 12 X 0.5MG | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 6 | SS | PARACETAMOL + CODEINE + PHENYLEPHRINE | ACETAMINOPHENCODEINEPHENYLEPHRINE | 1 | Unknown | 4 X 500MG PARACETAMOL/9.5MG CODEINE/5MG PHENYLEPHRINE | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 7 | SS | Magnesium | MAGNESIUM | 1 | Unknown | 10X3.74 MG | UNKNOWN | 0 | |||||||||
| 126470921 | 12647092 | 8 | SS | Paracetamol | ACETAMINOPHEN | 1 | Unknown | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126470921 | 12647092 | 1 | Atrial fibrillation |
| 126470921 | 12647092 | 2 | Product used for unknown indication |
| 126470921 | 12647092 | 3 | Product used for unknown indication |
| 126470921 | 12647092 | 4 | Product used for unknown indication |
| 126470921 | 12647092 | 5 | Product used for unknown indication |
| 126470921 | 12647092 | 6 | Product used for unknown indication |
| 126470921 | 12647092 | 7 | Product used for unknown indication |
| 126470921 | 12647092 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126470921 | 12647092 | LT |
| 126470921 | 12647092 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126470921 | 12647092 | Haemorrhage | |
| 126470921 | 12647092 | Heart rate irregular | |
| 126470921 | 12647092 | Hypotension | |
| 126470921 | 12647092 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |