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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127949831 | 12794983 | 1 | I | 20160722 | 20160915 | 20160929 | 20160929 | EXP | US-ELI_LILLY_AND_COMPANY-US201609006356 | ELI LILLY AND CO | 66.14 | YR | F | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127949831 | 12794983 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Subcutaneous | 20 UG, UNKNOWN | Y | U | C465010C | 21318 | 20 | UG | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127949831 | 12794983 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127949831 | 12794983 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127949831 | 12794983 | Agitation | |
| 127949831 | 12794983 | Back pain | |
| 127949831 | 12794983 | Bone pain | |
| 127949831 | 12794983 | Eating disorder | |
| 127949831 | 12794983 | Fatigue | |
| 127949831 | 12794983 | Irritability | |
| 127949831 | 12794983 | Nausea | |
| 127949831 | 12794983 | Neck pain | |
| 127949831 | 12794983 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 127949831 | 12794983 | 1 | 20160722 | 20160805 | 0 |