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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125671852 | 12567185 | 2 | F | 20140717 | 20160802 | 20160718 | 20160805 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-46603BI | BOEHRINGER INGELHEIM | 84.71 | YR | F | Y | 0.00000 | 20160805 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125671852 | 12567185 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 300 MG | 22512 | 150 | MG | CAPSULE | BID | ||||||
125671852 | 12567185 | 2 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Unknown | U | 0 | ||||||||||
125671852 | 12567185 | 3 | SS | LOVENOX | ENOXAPARIN SODIUM | 1 | Unknown | U | 0 | ||||||||||
125671852 | 12567185 | 4 | C | AMIODARONE | AMIODARONE | 1 | Oral | 200 MG | 0 | 200 | MG | QD | |||||||
125671852 | 12567185 | 5 | C | METOPROLOL SUCCINATE. | METOPROLOL SUCCINATE | 1 | Oral | 25 MG | 0 | 25 | MG | QD | |||||||
125671852 | 12567185 | 6 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | Unknown | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125671852 | 12567185 | 1 | Atrial fibrillation |
125671852 | 12567185 | 2 | Product used for unknown indication |
125671852 | 12567185 | 3 | Product used for unknown indication |
125671852 | 12567185 | 4 | Product used for unknown indication |
125671852 | 12567185 | 5 | Product used for unknown indication |
125671852 | 12567185 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125671852 | 12567185 | HO |
125671852 | 12567185 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125671852 | 12567185 | Gastrointestinal haemorrhage | |
125671852 | 12567185 | Shock haemorrhagic |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125671852 | 12567185 | 1 | 20120731 | 20140717 | 0 |