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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127359511 | 12735951 | 1 | I | 2016 | 20160901 | 20160912 | 20160912 | EXP | US-AMGEN-USASP2016117370 | AMGEN | 64.00 | YR | A | F | Y | 0.00000 | 20160912 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127359511 | 12735951 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, UNK ON SUNDAYS | 1066401 | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
| 127359511 | 12735951 | 2 | SS | BONIVA | IBANDRONATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 127359511 | 12735951 | 3 | C | VIVELLE-DOT | ESTRADIOL | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 5 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 6 | C | PROGESTERONE. | PROGESTERONE | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 8 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 9 | C | FISH OIL | FISH OIL | 1 | UNK | 0 | |||||||||||
| 127359511 | 12735951 | 10 | C | CORTISONE | CORTISONEHYDROCORTISONE | 1 | UNK | 0 | CREAM |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127359511 | 12735951 | 1 | Rheumatoid arthritis |
| 127359511 | 12735951 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127359511 | 12735951 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127359511 | 12735951 | Arthralgia | |
| 127359511 | 12735951 | Blood cholesterol increased | |
| 127359511 | 12735951 | Blood pressure abnormal | |
| 127359511 | 12735951 | Chills | |
| 127359511 | 12735951 | Condition aggravated | |
| 127359511 | 12735951 | Foot operation | |
| 127359511 | 12735951 | Gait disturbance | |
| 127359511 | 12735951 | Herpes virus infection | |
| 127359511 | 12735951 | Hyperkeratosis | |
| 127359511 | 12735951 | Inflammation | |
| 127359511 | 12735951 | Joint dislocation | |
| 127359511 | 12735951 | Malaise | |
| 127359511 | 12735951 | Mobility decreased | |
| 127359511 | 12735951 | Muscle strain | |
| 127359511 | 12735951 | Oropharyngeal pain | |
| 127359511 | 12735951 | Pain in extremity | |
| 127359511 | 12735951 | Papilloma viral infection | |
| 127359511 | 12735951 | Pityriasis rosea | |
| 127359511 | 12735951 | Skin discolouration | |
| 127359511 | 12735951 | Swelling | |
| 127359511 | 12735951 | Visual acuity reduced |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |