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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126197141 | 12619714 | 1 | I | 20160725 | 20160803 | 20160803 | EXP | PHHY2016AU105345 | SANDOZ | BARTON J, WONG A, GRAUDINS A. ANTI-XA ACTIVITY IN APIXABAN OVERDOSE: A CASE REPORT. CLINICAL TOXICOLOGY. 2016;1-6 | 53.00 | YR | M | Y | 0.00000 | 20160803 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126197141 | 12619714 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 35 MG, UNK | U | 77514 | 35 | MG | |||||||
126197141 | 12619714 | 2 | SS | BISOPROLOL | BISOPROLOL | 1 | Unknown | 105 MG, UNK | U | 0 | 105 | MG | |||||||
126197141 | 12619714 | 3 | SS | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 280 MG, UNK | U | 0 | 280 | MG | |||||||
126197141 | 12619714 | 4 | SS | APIXABAN | APIXABAN | 1 | Unknown | 200 MG, UNK | U | 0 | 200 | MG | |||||||
126197141 | 12619714 | 5 | SS | COLCHICINE. | COLCHICINE | 1 | Unknown | 6 MG, UNK | U | 0 | 6 | MG | |||||||
126197141 | 12619714 | 6 | SS | MAGNESIUM | MAGNESIUM | 1 | Unknown | 37.4 MG, UNK | U | 0 | 37.4 | MG | |||||||
126197141 | 12619714 | 7 | SS | ALCOHOL. | ALCOHOL | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126197141 | 12619714 | 1 | Product used for unknown indication |
126197141 | 12619714 | 2 | Product used for unknown indication |
126197141 | 12619714 | 3 | Product used for unknown indication |
126197141 | 12619714 | 4 | Atrial fibrillation |
126197141 | 12619714 | 5 | Product used for unknown indication |
126197141 | 12619714 | 6 | Product used for unknown indication |
126197141 | 12619714 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126197141 | 12619714 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126197141 | 12619714 | Haemorrhage | |
126197141 | 12619714 | Intentional overdose | |
126197141 | 12619714 | Poisoning |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |