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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126857641 | 12685764 | 1 | I | 20160627 | 20160812 | 20160825 | 20160825 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-067423 | BRISTOL MYERS SQUIBB | 89.21 | YR | M | Y | 0.00000 | 20160825 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126857641 | 12685764 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 1 U, PRN | U | 9218 | 1 | DF | TABLET | ||||||
126857641 | 12685764 | 2 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | U | 0 | ||||||||||
126857641 | 12685764 | 3 | C | LANSOX | LANSOPRAZOLE | 1 | Oral | UNK | U | 0 | CAPSULE | ||||||||
126857641 | 12685764 | 4 | C | DILATREND | CARVEDILOL | 1 | Oral | U | 0 | TABLET | |||||||||
126857641 | 12685764 | 5 | C | MOBIC | MELOXICAM | 1 | Oral | U | 0 | ||||||||||
126857641 | 12685764 | 6 | C | EUTIROX | LEVOTHYROXINE SODIUM | 1 | Oral | U | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126857641 | 12685764 | 1 | Atrial fibrillation |
126857641 | 12685764 | 2 | Product used for unknown indication |
126857641 | 12685764 | 3 | Product used for unknown indication |
126857641 | 12685764 | 4 | Product used for unknown indication |
126857641 | 12685764 | 5 | Product used for unknown indication |
126857641 | 12685764 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126857641 | 12685764 | HO |
126857641 | 12685764 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126857641 | 12685764 | Asthenia | |
126857641 | 12685764 | Overdose | |
126857641 | 12685764 | Rectal haemorrhage |
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 |
---|---|---|---|---|---|---|
126857641 | 12685764 | 1 | 20160101 | 20160627 | 0 |