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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125761272 | 12576127 | 2 | F | 20160606 | 20160719 | 20160720 | 20160801 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-055832 | BRISTOL MYERS SQUIBB | 75.53 | YR | M | Y | 83.00000 | KG | 20160801 | CN | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125761272 | 12576127 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 1.25 MG, QD | 13699.25 | MG | 9218 | 1.25 | MG | TABLET | QD | ||||
125761272 | 12576127 | 2 | C | LANOXIN | DIGOXIN | 1 | Oral | 1 U, UNK | U | 0 | 1 | DF | TABLET | ||||||
125761272 | 12576127 | 3 | C | DILATREND | CARVEDILOL | 1 | Oral | 1 U, UNK | U | 0 | 1 | DF | TABLET | ||||||
125761272 | 12576127 | 4 | C | NORVASC | AMLODIPINE BESYLATE | 1 | Oral | 1 U, UNK | U | 0 | 1 | DF | TABLET | ||||||
125761272 | 12576127 | 5 | C | LASIX | FUROSEMIDE | 1 | Oral | 1 U, UNK | U | 0 | 1 | DF | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125761272 | 12576127 | 1 | Atrial fibrillation |
125761272 | 12576127 | 2 | Cardiac failure |
125761272 | 12576127 | 3 | Hypertension |
125761272 | 12576127 | 4 | Hypertension |
125761272 | 12576127 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125761272 | 12576127 | OT |
125761272 | 12576127 | DE |
125761272 | 12576127 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125761272 | 12576127 | Cardiopulmonary failure | |
125761272 | 12576127 | Cerebral haemorrhage | |
125761272 | 12576127 | Epilepsy | |
125761272 | 12576127 | Respiratory disorder | |
125761272 | 12576127 | Subdural haematoma | |
125761272 | 12576127 | Subdural haematoma evacuation | |
125761272 | 12576127 | Tracheostomy |
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 |
---|---|---|---|---|---|---|
125761272 | 12576127 | 1 | 19860530 | 20160606 | 0 |