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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126003141 | 12600314 | 1 | I | 20160720 | 20160727 | 20160727 | EXP | PHHY2016TR102371 | SANDOZ | APARCI M, DOGAN M, YALCIN M, ISILAK Z, BICAKCI B. PROTON PUMP INHIBITORS SHOULD BE USED CAUTIOUSLY IN PATIENTS WITH ACUTE CORONARY SYNDROME. AMERICAN JOURNAL OF CARDIOLOGY. 2016;117:S71 | 72.00 | YR | F | Y | 0.00000 | 20160727 | OT | TR | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126003141 | 12600314 | 1 | PS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Intravenous (not otherwise specified) | 40 MG, QD | Y | 90296 | 40 | MG | QD | ||||||
| 126003141 | 12600314 | 2 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Intravenous (not otherwise specified) | 40 MG, BID | Y | 90296 | 40 | MG | BID | ||||||
| 126003141 | 12600314 | 3 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | 75 MG, QD | U | 0 | 75 | MG | QD | ||||||
| 126003141 | 12600314 | 4 | C | ACETYLSALICYLIC ACID | ASPIRIN | 1 | Unknown | 100 MG, QD | U | 0 | 100 | MG | QD | ||||||
| 126003141 | 12600314 | 5 | C | ATORVASTATIN | ATORVASTATIN | 1 | Oral | 20 MG, QD | U | 0 | 20 | MG | QD | ||||||
| 126003141 | 12600314 | 6 | C | ENOXAPARIN | ENOXAPARIN | 1 | Subcutaneous | 0.6 ML, BID | U | 0 | .6 | ML | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126003141 | 12600314 | 1 | Gastrointestinal haemorrhage |
| 126003141 | 12600314 | 3 | Product used for unknown indication |
| 126003141 | 12600314 | 4 | Product used for unknown indication |
| 126003141 | 12600314 | 5 | Product used for unknown indication |
| 126003141 | 12600314 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126003141 | 12600314 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126003141 | 12600314 | Anaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |