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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126701261 | 12670126 | 1 | I | 20160606 | 20160811 | 20160821 | 20160821 | EXP | US-ELI_LILLY_AND_COMPANY-US201608007306 | ELI LILLY AND CO | 70.99 | YR | F | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126701261 | 12670126 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Unknown | UNK, QD | Y | N | C462926D | 21318 | INJECTION | QD | |||||
| 126701261 | 12670126 | 2 | C | CALCIUM | CALCIUM | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126701261 | 12670126 | 1 | Osteoporosis |
| 126701261 | 12670126 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126701261 | 12670126 | OT |
| 126701261 | 12670126 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126701261 | 12670126 | Concussion | |
| 126701261 | 12670126 | Fall | |
| 126701261 | 12670126 | Head injury | |
| 126701261 | 12670126 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 126701261 | 12670126 | 1 | 201504 | 0 |