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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126023411 | 12602341 | 1 | I | 201606 | 20160718 | 20160728 | 20160728 | PER | US-AMGEN-USASL2016093428 | AMGEN | 76.00 | YR | E | F | Y | 0.00000 | 20160728 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126023411 | 12602341 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, QWK | U | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||
| 126023411 | 12602341 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 126023411 | 12602341 | 3 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK 7 DAY PACK | 0 | ||||||||||
| 126023411 | 12602341 | 4 | SS | MEDROL | METHYLPREDNISOLONE | 1 | Unknown | UNK | 0 | ||||||||||
| 126023411 | 12602341 | 5 | C | BYSTOLIC | NEBIVOLOL HYDROCHLORIDE | 1 | Unknown | 5 MG, QD | 0 | 5 | MG | QD | |||||||
| 126023411 | 12602341 | 6 | C | BYSTOLIC | NEBIVOLOL HYDROCHLORIDE | 1 | 10 MG, QD | 0 | 10 | MG | QD | ||||||||
| 126023411 | 12602341 | 7 | C | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 20/12.5MG IN THE MORNING | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126023411 | 12602341 | 1 | Rheumatoid arthritis |
| 126023411 | 12602341 | 2 | Product used for unknown indication |
| 126023411 | 12602341 | 3 | Pain |
| 126023411 | 12602341 | 5 | Hypertension |
| 126023411 | 12602341 | 7 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126023411 | 12602341 | Abdominal pain | |
| 126023411 | 12602341 | Adverse drug reaction | |
| 126023411 | 12602341 | Blood pressure increased | |
| 126023411 | 12602341 | Cushingoid | |
| 126023411 | 12602341 | Drug ineffective | |
| 126023411 | 12602341 | Drug intolerance | |
| 126023411 | 12602341 | Nausea | |
| 126023411 | 12602341 | Pain | |
| 126023411 | 12602341 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 126023411 | 12602341 | 3 | 20160616 | 20160623 | 0 |