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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127140192 | 12714019 | 2 | F | 20160507 | 20160919 | 20160905 | 20160928 | EXP | DE-PFIZER INC-2016302531 | PFIZER | 73.00 | YR | M | Y | 120.00000 | KG | 20160928 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127140192 | 12714019 | 1 | SS | ELIQUIS | APIXABAN | 1 | 5 MG, 2X/DAY | 860 | MG | U | 0 | 5 | MG | FILM-COATED TABLET | BID | ||||
| 127140192 | 12714019 | 2 | PS | IBUPROFEN. | IBUPROFEN | 1 | 600 MG, 1X/DAY | U | 18989 | 600 | MG | QD | |||||||
| 127140192 | 12714019 | 3 | C | PRAVASTATIN. | PRAVASTATIN | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
| 127140192 | 12714019 | 4 | C | LIORESAL | BACLOFEN | 1 | 5 MG, 3X/DAY | 0 | 5 | MG | TID | ||||||||
| 127140192 | 12714019 | 5 | C | TRILEPTAL | OXCARBAZEPINE | 1 | 600 MG, 2X/DAY | 0 | 600 | MG | BID | ||||||||
| 127140192 | 12714019 | 6 | C | CANDESARTAN | CANDESARTAN | 1 | 8 MG, 1X/DAY | 0 | 8 | MG | QD | ||||||||
| 127140192 | 12714019 | 7 | C | CARBIMAZOL HENNING | 2 | 10 MG, 2X/DAY | 0 | 10 | MG | BID | |||||||||
| 127140192 | 12714019 | 8 | C | KEPPRA | LEVETIRACETAM | 1 | 500 MG, 1X/DAY | 0 | 500 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127140192 | 12714019 | 1 | Cerebrovascular accident prophylaxis |
| 127140192 | 12714019 | 2 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127140192 | 12714019 | DE |
| 127140192 | 12714019 | HO |
| 127140192 | 12714019 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127140192 | 12714019 | Haematemesis | |
| 127140192 | 12714019 | Packed red blood cell transfusion | |
| 127140192 | 12714019 | Shock haemorrhagic | |
| 127140192 | 12714019 | Transfusion | |
| 127140192 | 12714019 | Upper gastrointestinal 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 |
|---|---|---|---|---|---|---|
| 127140192 | 12714019 | 1 | 20160212 | 20160507 | 0 | |
| 127140192 | 12714019 | 2 | 2012 | 0 |