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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118125652 | 11812565 | 2 | F | 20150927 | 20160816 | 20151208 | 20160819 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-082830 | BRISTOL MYERS SQUIBB | 87.21 | YR | M | Y | 0.00000 | 20160819 | CN | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118125652 | 11812565 | 1 | PS | COUMADINE | WARFARIN SODIUM | 1 | Unknown | 1 UNK, UNK | Y | 9218 | 1 | DF | TABLET | ||||||
118125652 | 11812565 | 2 | SS | LOVENOX | ENOXAPARIN SODIUM | 1 | Subcutaneous | 2 DF, BID | U | 0 | 2 | DF | SOLUTION FOR INJECTION | QD | |||||
118125652 | 11812565 | 3 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 5 MG, UNK | U | 0 | 5 | MG | QD | ||||||
118125652 | 11812565 | 4 | C | NEBIVOLOL. | NEBIVOLOL | 1 | Unknown | 1 UNK, UNK | U | 0 | 1 | DF | QD | ||||||
118125652 | 11812565 | 5 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118125652 | 11812565 | 1 | Deep vein thrombosis |
118125652 | 11812565 | 2 | Deep vein thrombosis |
118125652 | 11812565 | 3 | Product used for unknown indication |
118125652 | 11812565 | 4 | Product used for unknown indication |
118125652 | 11812565 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118125652 | 11812565 | OT |
118125652 | 11812565 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118125652 | 11812565 | Abscess drainage | |
118125652 | 11812565 | Cholecystitis acute | |
118125652 | 11812565 | General physical health deterioration | |
118125652 | 11812565 | Haematuria | |
118125652 | 11812565 | International normalised ratio increased | |
118125652 | 11812565 | Liver abscess | |
118125652 | 11812565 | Malnutrition | |
118125652 | 11812565 | Overdose | |
118125652 | 11812565 | Sepsis |
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 |
---|---|---|---|---|---|---|
118125652 | 11812565 | 1 | 20150929 | 0 | ||
118125652 | 11812565 | 2 | 20150930 | 20151004 | 0 |