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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125944791 | 12594479 | 1 | I | 20160702 | 20160713 | 20160726 | 20160726 | EXP | GB-AUROBINDO-AUR-APL-2016-09286 | AUROBINDO | 62.00 | YR | M | Y | 0.00000 | 20160726 | PH | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125944791 | 12594479 | 1 | PS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, ONCE A DAY | Y | U | 90540 | 75 | MG | QD | |||||
125944791 | 12594479 | 2 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | U | 0 | ||||||||||
125944791 | 12594479 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | U | 0 | ||||||||||
125944791 | 12594479 | 4 | C | GLIMEPIRIDE. | GLIMEPIRIDE | 1 | Unknown | U | 0 | ||||||||||
125944791 | 12594479 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
125944791 | 12594479 | 6 | C | MIXTARD /00806401/ | 2 | Unknown | U | 0 | |||||||||||
125944791 | 12594479 | 7 | C | OLMESARTAN | OLMESARTAN | 1 | Unknown | U | 0 | ||||||||||
125944791 | 12594479 | 8 | C | PREGABALIN. | PREGABALIN | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125944791 | 12594479 | 1 | Cardiovascular event prophylaxis |
125944791 | 12594479 | 2 | Product used for unknown indication |
125944791 | 12594479 | 3 | Product used for unknown indication |
125944791 | 12594479 | 4 | Product used for unknown indication |
125944791 | 12594479 | 5 | Product used for unknown indication |
125944791 | 12594479 | 6 | Product used for unknown indication |
125944791 | 12594479 | 7 | Product used for unknown indication |
125944791 | 12594479 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125944791 | 12594479 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125944791 | 12594479 | Duodenal ulcer haemorrhage | |
125944791 | 12594479 | Haematemesis |
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 |
---|---|---|---|---|---|---|
125944791 | 12594479 | 1 | 20160702 | 0 |