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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127285971 | 12728597 | 1 | I | 201607 | 20160811 | 20160909 | 20160909 | EXP | US-AMGEN-USASL2016105417 | AMGEN | 73.00 | YR | E | F | Y | 0.00000 | 20160909 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127285971 | 12728597 | 1 | PS | SENSIPAR | CINACALCET HYDROCHLORIDE | 1 | Oral | 30 MG, QD | Y | 1057501 | 21688 | 30 | MG | TABLET | QD | ||||
| 127285971 | 12728597 | 2 | C | FISH OIL | FISH OIL | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127285971 | 12728597 | 1 | Hyperparathyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127285971 | 12728597 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127285971 | 12728597 | Abdominal discomfort | |
| 127285971 | 12728597 | Abdominal pain | |
| 127285971 | 12728597 | Malaise | |
| 127285971 | 12728597 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 127285971 | 12728597 | 1 | 201607 | 0 |